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        HSPC142 Rabbit pAb (bs-18088R)  
        訂購熱線:400-901-9800
        訂購郵箱:sales@bioss.com.cn
        訂購QQ:  400-901-9800
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        50ul/1180.00元
        100ul/1980.00元
        200ul/2800.00元
        大包裝/詢價
        產品編號 bs-18088R
        英文名稱 HSPC142 Rabbit pAb
        中文名稱 乳腺癌易感基因復合物HSPC142抗體
        別    名 BABA1_HUMAN; babam1; BRCA1 A complex subunit MERIT40; BRISC and BRCA1-A complex member 1; C19orf62; FLJ20571; HSPC142; hypothetical protein LOC29086; Mediator of Rap80 interactions and targeting 40 kDa; Mediator of RAP80 interactions and targeting subunit of 40 kDa; MERIT 40; MERIT40; NBA1; New component of the BRCA1 A complex; New component of the BRCA1-A complex; Uncharacterized protein C19orf62.  
        研究領域 腫瘤  細胞生物  轉錄調節因子  糖尿病  表觀遺傳學  
        抗體來源 Rabbit
        克隆類型 Polyclonal
        克 隆 號
        交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Cat,Horse,Chinese Hamster, Orangutan,Elephant)
        產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
        not yet tested in other applications.
        optimal dilutions/concentrations should be determined by the end user.
        理論分子量 36 kDa
        檢測分子量
        細胞定位 細胞核 細胞漿 
        性    狀 Liquid
        濃    度 1mg/ml
        免 疫 原 KLH conjugated synthetic peptide derived from human HSPC142: 101-200/329 
        亞    型 IgG
        純化方法 affinity purified by Protein A
        緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
        保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
        注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
        PubMed PubMed
        產品介紹 Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf62 gene product has been provisionally designated C19orf62 pending further characterization.

        Function:
        Component of the BRCA1-A complex, a complex that specifically recognizes 'Lys-63'-linked ubiquitinated histones H2A and H2AX at DNA lesions sites, leading to target the BRCA1-BARD1 heterodimer to sites of DNA damage at double-strand breaks (DSBs). The BRCA1-A complex also possesses deubiquitinase activity that specifically removes 'Lys-63'-linked ubiquitin on histones H2A and H2AX. In the BRCA1-A complex, it is required for the complex integrity and its localization at DSBs. Probably also plays a role as a component of the BRISC complex, a multiprotein complex that specifically cleaves 'Lys-63'-linked ubiquitin. In these 2 complexes, it is probably required to maintain the stability of BRE/BRCC45 and help the 'Lys-63'-linked deubiquitinase activity mediated by BRCC3/BRCC36. component.

        Subcellular Location:
        Cytoplasm. Nucleus. Localizes at sites of DNA damage at double-strand breaks.

        Similarity:
        Belongs to the BABAM1 family.

        SWISS:
        Q9NWV8

        Gene ID:
        29086

        Database links:

        Entrez Gene: 29086 Human

        Entrez Gene: 68251 Mouse

        Entrez Gene: 290631 Rat

        Omim: 612766 Human

        SwissProt: Q9NWV8 Human

        SwissProt: Q3UI43 Mouse

        SwissProt: Q5XIJ6 Rat

        Unigene: 190722 Human

        Unigene: 21749 Mouse

        Unigene: 74107 Rat



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