BBS12 蛋白
(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].
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custom-made
BBS12
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
BBS12
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for BBS12 蛋白
Bardet-Biedl syndrome 12 (human) (Bbs12) 蛋白Bardet-Biedl syndrome 12 (Bbs12) 蛋白
Bardet-Biedl syndrome 12 (BBS12) 蛋白
Bardet-Biedl syndrome 12 (bbs12) 蛋白
Bardet-Biedl syndrome 12 L homeolog (bbs12.L) 蛋白
C4orf24 蛋白
DKFZP468P0511 蛋白
Gm407 蛋白
Gm721 蛋白
Gm1805 蛋白
RGD1561608 蛋白
RP23-137F6.2 蛋白
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