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    Rabbit Anti-DDI1/HRP Conjugated antibody (bs-14212R-HRP)
    訂購熱線:400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
    技術支持:techsupport@bioss.com.cn
    說 明 書: 100ul  
    100ul/2980.00元
    大包裝/詢價
    產品編號 bs-14212R-HRP
    英文名稱 Rabbit Anti-DDI1/HRP Conjugated antibody
    中文名稱 辣根過氧化物酶標記的DNA損傷誘導蛋白1抗體
    別    名 ddi1; DDI1 DNA damage inducible 1 homolog 1; DDI1_HUMAN; DNA-damage inducible 1, homolog 1; DNA-damage inducible protein 1; FLJ36017; OTTHUMP00000231644; Protein DDI1 homolog 1.  
    規格價格 100ul/2980元 購買        大包裝/詢價
    說 明 書 100ul  
    研究領域 細胞生物  細胞凋亡  細胞周期蛋白  泛素  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Rabbit, )
    產品應用 WB=1:500-2000 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 44kDa
    性    狀 Lyophilized or Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human DDI1
    亞    型 IgG
    純化方法 affinity purified by Protein A
    儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
    產品介紹 background:
    DDI1 is a 396 amino acid protein that contains one ubiquitin-like domain. The gene encoding DDI1 maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene.

    Similarity:
    Belongs to the DDI1 family.
    Contains 1 ubiquitin-like domain.

    Database links:

    Entrez Gene: 414301 Human

    Entrez Gene: 71829 Mouse

    Entrez Gene: 367012 Rat

    SwissProt: Human

    SwissProt: Q8WTU0 Human

    SwissProt: Q9DAF3 Mouse

    SwissProt: A0JPP7 Rat

    Unigene: 591941 Human

    Unigene: 141452 Mouse

    Unigene: 92290 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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