BBS12 抗体
(Bardet-Biedl Syndrome 12 (BBS12))
The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
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| BBS12 抗体 (Alexa Fluor 555) | 人 | 兔 Polyclonal |
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| BBS12 抗体 (Alexa Fluor 647) | 人 | 兔 Polyclonal |
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| BBS12 抗体 (Alexa Fluor 750) | 人 | 兔 Polyclonal |
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| BBS12 抗体 (Alexa Fluor 488) | 人 | 兔 Polyclonal |
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| BBS12 抗体 (Alexa Fluor 594) | 人 | 兔 Polyclonal |
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Aliases for BBS12 抗体
Bardet-Biedl syndrome 12 (human) (Bbs12) 抗体Bardet-Biedl syndrome 12 (Bbs12) 抗体
Bardet-Biedl syndrome 12 (BBS12) 抗体
Bardet-Biedl syndrome 12 (bbs12) 抗体
Bardet-Biedl syndrome 12 L homeolog (bbs12.L) 抗体
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