BBS7 抗体 (AA 85-135)
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北京 101111
Quick Overview for BBS7 抗体 (AA 85-135) (ABIN8119957)
抗原
See all BBS7 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 85-135
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原理
- BBS7 Antibody
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特异性
- This antibody detects endogenous levels of BBS7 at Human/Mouse
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from human BBS7 AA range: 85-135
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亚型
- IgG
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anti-Bardet-Biedl Syndrome 7 (BBS7) (Internal Region) antibody
BBS7 适用: 人, 小鼠, 大鼠 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 1-715) antibodyBBS7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (Internal Region) antibodyVerified BBS7 适用: 人, 大鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) antibodyBBS7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 574-672) antibodyBBS7 适用: 人 ELISA, WB 宿主: 小鼠 Monoclonal 2H6 unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 73-99), (N-Term) antibodyBBS7 适用: 人 WB 宿主: 兔 Polyclonal RB36934 unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 1-270) antibodyBBS7 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 289-393) antibodyBBS7 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 7 (BBS7) (AA 1-715) antibodyBBS7 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB 1:500-2000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C/1 year
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有效期
- 12 months
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- BBS7 (Bardet-Biedl Syndrome 7 (BBS7))
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别名
- BBS7
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背景
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Background: This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy, however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014],
Gene Name: BBS7 BBS2L1
Protein Name: BBS7
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基因ID
- 55212
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UniProt
- Q8IWZ6
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途径
- Hedgehog Signaling
抗原
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