HFM1 Antibody
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								中文名稱:HFM1兔多克隆抗體
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								貨號:CSB-PA010325LA01HU
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								規(guī)格:¥880
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								圖片:
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								其他:
產品詳情
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											產品名稱:Rabbit anti-Homo sapiens (Human) HFM1 Polyclonal antibody
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											Uniprot No.:
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											基因名:HFM1
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											別名:HFM1 antibody; SEC3D1Probable ATP-dependent DNA helicase HFM1 antibody; EC 3.6.4.12 antibody; SEC63 domain-containing protein 1 antibody
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											宿主:Rabbit
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											反應種屬:Human
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											免疫原:Recombinant Human Probable ATP-dependent DNA helicase HFM1 protein (121-420AA)
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											免疫原種屬:Homo sapiens (Human)
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											標記方式:Non-conjugated本頁面中的產品,HFM1 Antibody (CSB-PA010325LA01HU),的標記方式是Non-conjugated。對于HFM1 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
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											產品提供形式:Liquid
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											應用范圍:ELISA, IHC
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											推薦稀釋比:Application Recommended Dilution IHC 1:20-1:200 
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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.
相關產品
靶點詳情
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											功能:Required for crossover formation and complete synapsis of homologous chromosomes during meiosis.
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											基因功能參考文獻:- Data suggest that HFM1 gene might be associated with primary ovarian insufficiency in Chinese population. PMID: 26679638
- Exome sequencing of two Chinese sisters with primary ovarian insufficiency and their parents identified a shared compound heterozygous mutation in a meiotic gene, HFM1, which encodes a protein necessary for homologous recombination of chromosomes. PMID: 24597873
- hHFM1 is the evolutionally conserved putative human DNA helicase, which may function as a modulator for genome integrity in germ-line tissues. PMID: 17286053
 
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											相關疾病:Premature ovarian failure 9 (POF9)
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											蛋白家族:Helicase family, SKI2 subfamily
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											組織特異性:Preferentially expressed in testis and ovary.
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											數據庫鏈接:
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