ENDOD1 Rabbit pAb, Biotin conjugated(bs-14591R-Bio)-100ul

ENDOD1 Rabbit pAb, Biotin conj

ugated(bs-14591R-Bio)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-14591R-Bio
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-14591R-Bio
    英文名称ENDOD1 Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的核酸内切酶结构域蛋白1抗体
    英文别名C85344; ENDD1_HUMAN; Endonuclease domain containing 1; Endonuclease domain-containing 1 protein; KIAA0830.
    产品应用IHC-P=1:100-500, IHC-F=1:100-500, ICC/IF=1:100-500, ELISA=1:5000-10000, IF=1:100-500

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human ENDOD1
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Epigenetics and Nuclear Signaling > Chromatin Binding Proteins > DNA / RNA binding

    亚细胞定位Secreted.
    相似性Belongs to the DNA/RNA non-specific endonuclease family.
    功能May act as a DNase and a RNase.
    保存条件Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料ENDOD1 is a 500 amino acid secreted protein that belongs to the DNA/RNA non-specific endonuclease family. ENDOD1 is thought to act as a DNase and an RNase. The gene that encodes ENDOD1 maps to human chromosome 11, which comprises approximately 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, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}
    {ICC/IF}{1:100-500}
    {ELISA}{1:5000-10000}
    {IF}{1:100-500}

     

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