Search result for 'form '.
Viewing records 301 to 350 of 521 hits.
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N16674
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Name: YNACS7YCACS7 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16675
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Name: YNACS8YCACS1 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16676
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Name: YNACS8YCACS2 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16677
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Name: YNACS8YCACS4 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16678
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Name: YNACS8YCACS5 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16679
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Name: YNACS8YCACS6 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16680
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Name: YNACS8YCACS7 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16681
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Name: YNACS8YCACS8 |
Price:
£11.00
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Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16682
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Name: YNACS9YCACS1 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16683
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Name: YNACS9YCACS2 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16684
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Name: YNACS9YCACS4 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16685
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Name: YNACS9YCACS5 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
|
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16686
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Name: YNACS9YCACS6 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16687
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Name: YNACS9YCACS7 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16688
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Name: YNACS9YCACS8 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
|
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16689
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Name: YNACS9YCACS9 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16690
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Name: YNACS11YCACS1 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16691
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Name: YNACS11YCACS4 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16692
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Name: YNACS11YCACS5 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16693
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Name: YNACS11YCACS6 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
|
|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16694
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Name: YNACS11YCACS7 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16695
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Name: YNACS11YCACS8 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16696
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Name: YNACS11YCACS9 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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|
Stock type: individual line
|
Material type: seed
|
|
Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N16697
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Name: YNACS11YCACS11 |
Price:
£11.00
|
Donor
- University of California, Berkeley Athanasios Theologis
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Stock type: individual line
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Material type: seed
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Description YN (the N-terminus of Citrine YFP with Q69M mutation (Griesbeck et al., J Biol Chem 2001)) and YC (the C-terminus of YFP) were used to make the N-terminal fusion and C-terminal fusion proteins for Bimolecular Fluorescence Complementation (BiFC), respectively. Aside from the T7 tag, YNACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP132 vector. Aside form the His tag, YCACS constructs contained ACS coding sequence and ACS 3' UTR under control of the corresponding ACS promoter in pPZP122 vector. Each N-terminal BiFC construct in pPZP132 vector and each C-terminal BiFC construct in pPZP122 were separately introduced in the pentuple2 mutant acs2-1acs4-1acs5-2acs6-1acs9-1 (CS16644) by transformation. The single identified homozygous line of pentuple 2 mutant transformed with the N-terminal BiFC construct was crossed to the single identified homozygous line of pentuple 2 mutant transformed with the C-terminal BiFC construct.
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N25248
|
Name: deformed root hairs 3 |
Price:
£11.00
|
Donor
- University of Zurich Christoph Ringli
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Locus
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Stock type: individual line
|
Material type: seed
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Description Impaired root hair development; seedlings form root hairs in a regular pattern; length of the hair proper is not affected, but side branches develop from the enlarged bases; backcrossed 3 times to C24.
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N25249
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Name: deformed root hairs 4 |
Price:
£11.00
|
Donor
- University of Zurich Christoph Ringli
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Locus
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Stock type: individual line
|
Material type: seed
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Description Impaired root hair development; seedlings form root hairs in a regular pattern, but significantly shorter than in the wild type; root hair appears normal beside the reduced length; backcrossed 3 times to C24.
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N25252
|
Name: deformed root hairs 7 |
Price:
£11.00
|
Donor
- University of Zurich Christoph Ringli
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Locus
|
Stock type: individual line
|
Material type: seed
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|
Description Impaired root hair development; seedlings form root hairs in a regular pattern, but significantly shorter than in the wild type; develops two different types of root hair structures: relatively short stumps with a clearly wider diameter than wild type hairs and longer hair structures which are wider in the lower half of the root hair proper while the upper half is wild type like; backcrossed 3 times to C24.
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N30916
|
Name: NFB1 |
Price:
£11.00
|
Donor
- University of Arizona Natalie Doetsch
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Locus
|
Stock type: individual line
|
Material type: seed
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|
Description homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
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Phenotype
homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
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N30917
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Name: NFB1 |
Price:
£11.00
|
Donor
- University of Arizona Natalie Doetsch
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
|
Phenotype
homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
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N30918
|
Name: NFB1 |
Price:
£11.00
|
Donor
- University of Arizona Natalie Doetsch
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
|
Phenotype
homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
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N30919
|
Name: NFB1 |
Price:
£11.00
|
Donor
- University of Arizona Natalie Doetsch
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
|
Phenotype
homologous to human CAF1 subunit B or yeast CAC2, the p60 subunit s of human and yeast chromatin assembly factor I , respectively. Human CAF1 is composed of three subunits that are 150 kd, 60 kd and 48 kd in size. The smallest subunit dissociates during G1 phase of the cell cycle. CAF1 is thought to deposit histones H3 and H4 onto newly replicated DNA such that histone H2A and H2B can then bind to form nucleosome core particles.
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N42994
|
Name: SLAT Filter Type 2 - NASC style |
Price:
£15.00
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Donor
- University of Nottingham Sean May
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Stock type: individual line
|
Material type: seed
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Description filter.Filter type 2: NASC style filter representing 60,000 lines (WITH MARKER); uses the original Sainsbury laboratory DNAs, and the original SL IPCR products; rearrayed in a linear form for ease of picking pools.
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N69096
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Name: p35S:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
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Stock type: individual line
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Material type: seed
|
|
Description The 35S promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69097
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Name: pCER5:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The CER5 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69098
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Name: pCO2:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
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|
Stock type: individual line
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Material type: seed
|
|
Description The CO2 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69099
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Name: pKAT1:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
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|
Stock type: individual line
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Material type: seed
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Description The KAT1 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69100
|
Name: pLAT52:HF-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
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Material type: seed
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Description The Solanum lycopersicum LAT52 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69101
|
Name: pPEP:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The PEP promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
|
N69102
|
Name: pRBCS:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The RBSC promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
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N69103
|
Name: pRPL11C:HF-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The RPL11C promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
|
N69104
|
Name: pRPL11C:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The RPL11C promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
|
Phenotype
No visible phenotype.
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N69105
|
Name: pSCR:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The SCR promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
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Phenotype
No visible phenotype.
|
N69106
|
Name: pSUC2:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The SUC2 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
|
Phenotype
No visible phenotype.
|
N69107
|
Name: pSULTR2;1:HF-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The SULTR2;1 promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
|
Phenotype
No visible phenotype.
|
N69108
|
Name: pWOL:HF-GFP-RPL18 |
Price:
£11.00
|
Donor
- University of California, Riverside Julia Bailey-Serres
|
|
Stock type: individual line
|
Material type: seed
|
|
Description The WOL promoter sequence was cloned into pENTR/D-TOPO. The TMV omega leader sequence, His6-FLAG tag, sGFP, coding region of RPL18B and 3 UTR of the OSC gene were cloned into a modified pPZP111 to form the vector construct, pGATA:HF-sGFP-RPL18. Following recombination, the Col-0 plant was transformed using the floral dip method; kanamycin resistant. This line is homozygous for the insertion and the insertion site is known. Users are strongly encouraged to confirm the genotype by use of genomic PCR. A primer list and protocols for the use of these lines will be posted on the donor's website (see URL link).
|
Phenotype
No visible phenotype.
|
N69886
|
Name: 69886 |
Price:
£11.00
|
Donor
- Leiden University Bert J. van der Zaal
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Phosphomimetic form of RACK1A, RACK1A (S122D/T162E), driven by the native promoter of RACK1A in pGWB40 was transformed into the rack1a-2 (CS68987) mutant background. Kanamycin and Hygromycin resistant. Genotype of transgene is unknown.
|
Phenotype
Hypersensitivity to glucose. Reduced number of rosette leaves, late flowering.
|
N69887
|
Name: 69887 |
Price:
£11.00
|
Donor
- Leiden University Bert J. van der Zaal
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Phosphomimetic form of RACK1A, RACK1A (S122D/T162E), driven by the native promoter of RACK1A in pGWB40 was transformed into the rack1a-2 (CS68987) mutant background. Kanamycin and Hygromycin resistant. Genotype of transgene is unknown.
|
Phenotype
Hypersensitivity to glucose. Reduced number of rosette leaves, late flowering.
|
N69888
|
Name: 69888 |
Price:
£11.00
|
Donor
- Leiden University Bert J. van der Zaal
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Phosphorylation-dead form of RACK1A, RACK1A (S122A/T162A), driven by the native promoter of RACK1A in pGWB40 was transformed into the rack1a-2 (CS68987) mutant background. Kanamycin and Hygromycin resistant. Genotype of transgene is unknown.
|
Phenotype
No visible phenotype
|
N69889
|
Name: 69889 |
Price:
£11.00
|
Donor
- Leiden University Bert J. van der Zaal
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Phosphorylation-dead form of RACK1A, RACK1A (S122A/T162A), driven by the native promoter of RACK1A in pGWB40 was transformed into the rack1a-2 (CS68987) mutant background. Kanamycin and Hygromycin resistant. Genotype of transgene is unknown.
|
Phenotype
No visible phenotype
|
Donor
- University of Pennsylvania Scott Poethig
|
|
Stock type: individual line
|
Material type: seed
|
|
Description line transformed with the enhancer trap vector GAL4-VP16 under the regulation of a minimal CaMV 35S promoter; expression of this vector is monitored by the reporter gene UAS::mGFP5-ER, an endoplasmic reticulum ER-localized form of the GFP gene; no visible phenotype; kanamycin resistant; T4 generation.
|
Phenotype
no visible phenotype
|
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