VWA3B Antibody, FITC conjugated
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中文名稱:VWA3B兔多克隆抗體, FITC偶聯(lián)
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貨號:CSB-PA681377LC01HU
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規(guī)格:¥880
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) VWA3B Polyclonal antibody
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Uniprot No.:
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基因名:VWA3B
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別名:VWA3B antibody; von Willebrand factor A domain-containing protein 3B antibody; VWA domain-containing protein 3B antibody
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宿主:Rabbit
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反應(yīng)種屬:Human
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免疫原:Recombinant Human von Willebrand factor A domain-containing protein 3B protein (1-160AA)
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免疫原種屬:Homo sapiens (Human)
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標(biāo)記方式:FITC
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克隆類型:Polyclonal
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抗體亞型:IgG
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純化方式:>95%, Protein G purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
產(chǎn)品提供形式:Liquid
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期: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.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
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靶點詳情
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基因功能參考文獻(xiàn):
- Mutated VWA3B was found to be likely associated with cerebellar degeneration with intellectual disability. Although a rare cause of cerebellar degeneration, these findings indicate a critical role for VWA3B in the apoptosis pathway in neuronal tissues. PMID: 26157035
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相關(guān)疾?。?/div>Spinocerebellar ataxia, autosomal recessive, 22 (SCAR22)亞細(xì)胞定位:Cytoplasm.數(shù)據(jù)庫鏈接:
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