Bardet-Biedl Syndrome 4 (BBS4) Peptide
BBS4
适用: 哺乳动物
宿主: 合成
BP, WB, IHC
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- 抗原 See all BBS4 products
- BBS4 (Bardet-Biedl Syndrome 4 (BBS4))
- 蛋白类型
- Synthetic
- 宿主
- 哺乳动物
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- 序列
- YVQALIFRLE GNIQESLELF QTCAVLSPQS ADNLKQVARS LFLLGKHKAA
- 产品特性
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A synthetic peptide for use as a blocking control in assays to test for specificity of BBS4 antibody,
Alternative Names: BBS4 control peptide, BBS4 antibody Blocking Peptide, Anti-BBS4 Blocking Peptide, Bardet-Biedl Syndrome 4 Blocking Peptide
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- 应用备注
- Optimal conditions should be determined by the investigator
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- 缓冲液
- PBS
- 注意事项
- Avoid repeated freeze/thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- Store at -20 °C long term.
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- 抗原
- BBS4 (Bardet-Biedl Syndrome 4 (BBS4))
- 别名
- CG13232 Peptide, Dmel\\CG13232 Peptide, zgc:152964 Peptide, AW537059 Peptide, AW742241 Peptide, D9Ertd464e Peptide, Bardet-Biedl syndrome 4 Peptide, bardet-biedl syndrome 4 Peptide, Bardet-Biedl syndrome 4 (human) Peptide, BBS4 Peptide, bbs4 Peptide, Bbs4 Peptide
- 背景
- 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.
- 分子量
- 58 kDa
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