Bardet-Biedl Syndrome 4 (BBS4) (N-Term) Peptide
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Quick Overview for Bardet-Biedl Syndrome 4 (BBS4) (N-Term) Peptide (ABIN5672066)
抗原
宿主
资源
应用范围
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蛋白结构域
- N-Term
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序列
- TESQKPRQKK APEFPILEKQ NWLIHLHYIR KDYEACKAVI KEQLQETQGL
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产品特性
- This is a synthetic peptide designed for use in combination with anti- BBS4 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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储存条件
- -20 °C
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储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- BBS4 (Bardet-Biedl Syndrome 4 (BBS4))
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背景
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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. 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. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants.
Protein Size: 519 -
基因ID
- 585
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NCBI登录号
- NM_001252678, NP_001239607
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UniProt
- Q96RK4
抗原
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