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BBS12


Official Full Name
Bardet-Biedl syndrome 12
Organism
Homo sapiens
Gene ID
166379
Background
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]
Synonyms
C4orf24

Cat.No. Product Name Price
SHG092129 shRNA set against Mouse Bbs12(NM_001008502.2) Inquiry
SHG092135 shRNA set against Human BBS12(NM_152618.2) Inquiry
SHH245130 shRNA set against Human BBS12 (NM_152618.2) Inquiry
SHH245134 shRNA set against Mouse BBS12 (NM_001008502.2) Inquiry
Cat.No. Product Name Price
CDCG010609 Mouse BBS12 ORF clone(NM_001255992.1) Inquiry
CDFG009536 Human BBS12 cDNA Clone(NM_152618.2) Inquiry
CDFH001671 Human BBS12 cDNA Clone(NM_001178007.1) Inquiry
MiUTR1H-00824 BBS12 miRNA 3'UTR clone Inquiry
MiUTR1M-01988 BBS12 miRNA 3'UTR clone Inquiry
CDCB183469 Rabbit BBS12 ORF clone (XM_002717237.2) Inquiry
CDCL211887 Mouse Bbs12 ORF Clone(NM_001008502.2) Inquiry
CDCR033343 Human BBS12 ORF clone (NM_152618.2) Inquiry
CDCR357190 Human BBS12 ORF Clone(NM_001178007.1) Inquiry
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