BBS5 蛋白
(Bardet-Biedl Syndrome 5 (BBS5))
This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized. [provided by RefSeq, Jul 2008].
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7 results
custom-made
BBS5
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
BBS5
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 BBS5 蛋白
Bardet-Biedl syndrome 5 (bbs5) 蛋白Bardet-Biedl syndrome 5 (BBS5) 蛋白
Bardet-Biedl syndrome 5 (Bbs5) 蛋白
Bardet-Biedl syndrome 5 (human) (Bbs5) 蛋白
1700049I01Rik 蛋白
2700023J09Rik 蛋白
zgc:56578 蛋白
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