BBS12 Polyclonal Antibody

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.

Research Area: Cancer, Metabolism, Neuroscience

Synonyms:
Bardet Biedl syndrome 12 protein, Bardet-Biedl syndrome 12 (human), Bardet-Biedl syndrome 12 protein, Bardet-Biedl syndrome 12 protein homolog, BBS12, BBS12 gene, BBS12, C4orf24, FLJ35630, FLJ41559, Gm1805, Gm407, Gm721, RP23-137F6.2

Immunogen: Synthetic peptide of human BBS12

Swissprot: Q6ZW61
Gene Accession: NP689831

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 0.9 mg/mL
Dilution: IHC 1:40-1:200, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.