| 产品详情 |
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| Product Name | Bardet-Biedl Syndrome 4 (BBS4) peptide |
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| Description | 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 mental retardation. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's 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. |
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| Size | 100 µg |
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| Concentration | n/a |
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| Applications | Western Blotting (WB),Immunohistochemistry (IHC),Blocking Peptide (BP) |
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| Other Names | CG13232|Dmel\\CG13232|zgc:152964|AW537059|AW742241|D9Ertd464e |
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| Gene, Accession, CAS # | n/a |
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| Catalog # | ABIN940364 |
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| Price | |
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| Order / More Info | Bardet-Biedl Syndrome 4 (BBS4) peptide from ANTIBODIES-ONLINE GmbH |
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| Product Specific References | n/a |
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| 产品资料 |
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