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BBS5
Bardet-Biedl syndrome 5DKFZp762I194
This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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| Proteintech Group |  14569-1-AP |
22 references | Polyclonal |
WB
EL
IP
IHC
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| Invitrogen Antibodies | 14569-1-AP |
Polyclonal |
WB
ICC
IP
IHC
OA
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| NovoPro Bioscience Inc. | 108372 |
Polyclonal |
WB
EL
ICC
IP
IHC
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| FineTest Biotech | FNab00819 |
Polyclonal |
WB
EL
ICC
IP
IHC
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| antibodies-online | ABIN2838514 |
3 references | Polyclonal |
WB
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