TCTN3 Antibody
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货号:CSB-PA747352LA01HU
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规格:¥440
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促销:
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图片:
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Western Blot
Positive WB detected in: HEK293 whole cell lysate, A549 whole cell lysate, HepG2 whole cell lysate, Rat heart tissue, Rat liver tissue, Rat stomach tissue
All lanes: TCTN3 antibody at 3.5µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 67, 48, 23, 51 kDa
Observed band size: 67, 51 kDa -
Immunofluorescent analysis of HepG2 cells using CSB-PA747352LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) TCTN3 Polyclonal antibody
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Uniprot No.:Q6NUS6
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基因名:TCTN3
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别名:C10orf61 antibody; Chromosome 10 open reading frame 61 antibody; DKFZP564D116 antibody; JBTS18 antibody; OFD4 antibody; TCTN3 antibody; TECT3 antibody; TECT3_HUMAN antibody; Tectonic 3 antibody; Tectonic 3 precursor antibody; Tectonic family member 3 antibody; Tectonic-3 antibody
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宿主:Rabbit
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反应种属:Human, Rat
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免疫原:Recombinant Human Tectonic-3 protein (348-472AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,TCTN3 Antibody (CSB-PA747352LA01HU),的标记方式是Non-conjugated。对于TCTN3 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IF
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 IF 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Part of the tectonic-like complex which is required for tissue-specific ciliogenesis and may regulate ciliary membrane composition. May be involved in apoptosis regulation. Necessary for signal transduction through the sonic hedgehog (Shh) signaling pathway.
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基因功能参考文献:
- TCTN3 mutations cause Mohr-Majewski syndrome. PMID: 22883145
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相关疾病:Orofaciodigital syndrome 4 (OFD4); Joubert syndrome 18 (JBTS18)
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亚细胞定位:Membrane; Single-pass type I membrane protein.
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蛋白家族:Tectonic family
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数据库链接:
HGNC: 24519
OMIM: 258860
KEGG: hsa:26123
STRING: 9606.ENSP00000265993
UniGene: Hs.438991
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