Explore
Validate
LearnTissue expression
Cell line expression
Protein structure
BBS2
Bardet-Biedl syndrome 2BBS
This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. 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 forms a multiprotein BBSome complex with seven other BBS proteins. [provided by RefSeq, Oct 2014]
Top validated antibodies |
|||||
| Proteintech Group |  11188-2-AP |
12 references | Polyclonal |
WB
EL
ICC
IP
|
|
| Invitrogen Antibodies | 11188-2-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
|
||
| NovoPro Bioscience Inc. | 108369 |
Polyclonal |
WB
EL
ICC
IP
|
||
| Wuhan Fine Biotech Co., Ltd. | FNab00815 |
Polyclonal |
WB
EL
ICC
IP
|
||
| Cusabio Biotech Co., Ltd | CSB-PA866303ESR1HU |
Polyclonal |
WB
EL
IHC
|
||
All Antibodies
Filters
Enhanced validation Supportive data in Antibodypedia Data presented on provider website
Data in Antibodypedia (inconclusive) Recommended by provider