C12orf57 Antibody
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中文名稱:C12orf57兔多克隆抗體
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貨號:CSB-PA859105LA01HU
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規(guī)格:¥440
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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) C12orf57 Polyclonal antibody
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Uniprot No.:
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基因名:C12orf57
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別名:C10_HUMAN antibody; C12orf57 antibody; Protein C10 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 Protein C10 protein (2-126AA)
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免疫原種屬:Homo sapiens (Human)
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標記方式:Non-conjugated
本頁面中的產(chǎn)品,C12orf57 Antibody (CSB-PA859105LA01HU),的標記方式是Non-conjugated。對于C12orf57 Antibody,我們還提供其他標記。見下表:
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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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應(yīng)用范圍:ELISA
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Protocols:
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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.
相關(guān)產(chǎn)品
靶點詳情
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功能:In brain, may be required for corpus callosum development.
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基因功能參考文獻:
- Exome sequencing identifies compound heterozygous mutations in C12orf57 in two siblings with severe intellectual disability, hypoplasia of the corpus callosum, chorioretinal coloboma, and intractable seizures. PMID: 24798461
- The findings strongly support the candidacy of C12orf57 as a gene that is mutated in a distinct syndromic form of colobomatous microphthalmia in humans. PMID: 23453665
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相關(guān)疾病:Temtamy syndrome (TEMTYS)
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亞細胞定位:Cytoplasm.
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蛋白家族:UPF0456 family
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組織特異性:Ubiquitously expressed, with higher expression in lung and fetal brain.
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數(shù)據(jù)庫鏈接:
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