IMPAD1 Rabbit pAb, Biotin conjugated(bs-6248R-Bio)-100ul

IMPAD1 Rabbit pAb, Biotin conj

ugated(bs-6248R-Bio)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-6248R-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-6248R-Bio
    英文名称IMPAD1 Rabbit pAb, Biotin conjugated
    中文名称Biotin标记的肌醇单磷酸酶IMPA3抗体
    英文别名IMP 3; IMPA3; IMPase 3; Inositol monophosphatase domain containing protein 1; Myo inositol monophosphatase A3.
    产品应用WB=1:500-2000

    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 IMPAD1
    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

    Cancer > Signal transduction > Protein phosphorylation

    Cardiovascular > Lipids / Lipoproteins > Lipid Metabolism > Hydrolysis

    Metabolism > Pathways and Processes > Metabolic signaling pathways > Lipid and lipoprotein metabolism > Hydrolysis

    Signal Transduction > Metabolism > Lipid metabolism

    亚细胞定位Golgi apparatus, trans-Golgi network membrane; Single-pass type II membrane protein.
    翻译后修饰Contains N-linked glycan resistant to endoglycosydase H.
    相似性Belongs to the inositol monophosphatase family.
    功能May play a role in the formation of skeletal elements derived through endochondral ossification, possibly by clearing adenosine 3',5'-bisphosphate produced by Golgi sulfotransferases during glycosaminoglycan sulfation
    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This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

     

    应用推荐稀释比例
    {WB}{1:500-2000}

     

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