BBS9 antibody
Product Specifications
Background
The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This ciliogenic function is mediated in part by the Rab8 GDP/GTP exchange factor, which localizes to the basal body and contacts the BBSome. Rab8 (GTP) enters the primary cilium and promotes extension of the ciliary membrane. Firstly the BBSome associates with the ciliary membrane and binds to RAB3IP/Rabin8, the guanosyl exchange factor (GEF) for Rab8 and then the Rab8-GTP localizes to the cilium and promotes docking and fusion of carrier vesicles to the base of the ciliary membrane. Required for proper BBSome complex assembly and its ciliary localization.
Synonyms
Protein PTHB1|Bardet-Biedl syndrome 9 protein|Parathyroid hormone-responsive B1 gene protein|BBS9|PTHB1
Gene ID
27241
UniProt
Q3SYG4
Host
Rabbit
Reactivity
Human, Mouse
Immunogen
Bardet-Biedl syndrome 9
Target
BBS9
Clonality
Polyclonal
Isotype
IgG
Applications
ELISA, IHC, IF, WB, IP
Field of Research
Neuroscience
Purification
Immunogen affinity purified
Dilution
WB: 1:1000-1:6000; IP: 1:500-1:3000; IHC: 1:50-1:500; IF: 1:50-1:500
Purity
≥95% as determined by SDS-PAGE
Form
Liquid
Molecular Weight
60 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Tested Applications
ELISA, IHC, IF, WB, IP
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