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Antibodies

BBS10 antibody - C-terminal region

Product Sizes
25ul
£177.00
ARP59803-P050-25UL
100 ul
£412.00
ARP59803-P050-100UL
About this Product
SKU:
ARP59803-P050
Additional Names:
C12orf58
Clonality:
Polyclonal
Concentration:
0.5 mg/ml
Extra Details:
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration; obesity; polydactyly; renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies; ciliary axonemes; and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone; this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10.
Gene Details:
Bardet-Biedl syndrome 10
Host:
Rabbit
Immunogen:
The immunogen is a synthetic peptide directed towards the C terminal region of human BBS10
Molecular Weight:
81kDa
Protein Details:
Bardet-Biedl syndrome 10 protein
Purification:
Affinity Purified
Shipping Conditions:
Blue Ice
Storage Conditions:
For short term use; store at 2-8C up to 1 week. For long term storage; store at -20C in small aliquots to prevent freeze-thaw cycles.
Supplier:
Aviva Systems Biology
Type:
Antibodies: Polyclonal Antibody