BBS7 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
BBS7
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
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- 抗原 See all BBS7 蛋白
- BBS7 (Bardet-Biedl Syndrome 7 (BBS7))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 2
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This BBS7 protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human BBS7 (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product BBS7 蛋白
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Bardet-Biedl Syndrome 7 (BBS7) (AA 1-715) protein (GST tag)
BBS7 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AA, AP
Bardet-Biedl Syndrome 7 (BBS7) (AA 574-672) protein (GST tag)BBS7 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AA, AP
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- BBS7 (Bardet-Biedl Syndrome 7 (BBS7))
- 别名
- Bbs7 (BBS7 产品)
- 别名
- BBS7 Protein, bbs2l1 Protein, BBS2L1 Protein, id:ibd5048 Protein, zgc:153772 Protein, 8430406N16Rik Protein, Bardet-Biedl syndrome 7 Protein, bardet-biedl syndrome 7 Protein, Bardet-Biedl syndrome 7 L homeolog Protein, Bardet-Biedl syndrome 7 (human) Protein, BBS7 Protein, bbs7 Protein, MICPUN_100192 Protein, MICPUCDRAFT_16331 Protein, bbs7.L Protein, Bbs7 Protein
- 背景
- This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014].
- 分子量
- 75.3 kDa
- NCBI登录号
- NP_060660
- 途径
- Hedgehog Signaling
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