FAM20C Rabbit pAb, AP conjugated(bs-12376R-AP)-100ul

FAM20C Rabbit pAb, AP conjugat

ed(bs-12376R-AP)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-12376R-AP
  • 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-12376R-AP
    英文名称FAM20C Rabbit pAb, AP conjugated
    中文名称AP标记的胞外分泌型丝氨酸/苏氨酸蛋白激酶FAM20C抗体
    英文别名C76981; Dentin matrix protein 4; DKFZp547C074; DMP-4; DMP4; DMP4_HUMAN; Extracellular serine/threonine protein kinase Fam20C; Fam20c; Family with sequence similarity 20 member C; GEF CK; Golgi enriched fraction casein kinase; Protein FAM20C; RNS antibod.
    产品应用IHC-P=1:100-500, IHC-F=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 FAM20C
    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

    Developmental Biology > Organogenesis > Skeletal development > Bone

    Signal Transduction > Cytoskeleton / ECM > Extracellular Matrix > ECM Proteins > Other ECM Proteins

    Signal Transduction > Cytoskeleton / ECM > Extracellular Matrix > Structures > Bone

    Signal Transduction > Signaling Pathway > Calcium Signaling > Calcium Binding Proteins

    Stem Cells > Mesenchymal Stem Cells > Osteogenesis

    亚细胞定位Secreted.
    组织特异性Widely expressed.
    相似性Belongs to the FAM20 family.
    功能Calcium-binding protein which may play a role in dentin mineralization.
    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The FAM20 proteins are a family of secreted proteins that regulate differentiation and function of hematopoietic and other tissues. FAM20C, also known as DMP4 (Dentin matrix protein 4), is a 570 amino acid secreted protein that binds calcium and may play a role in dentin mineralization. Defects in the gene encoding FAM20C are the cause of Raine syndrome (Lethal osteosclerotic bone dysplasia), an autosomal recessive osteosclerotic bone dysplasia, that is characterized by generalized osteosclerosis, microencephaly and craniofacial dysplasia. Usually, affected individuals survive only days or weeks. The mutations of the FAM20C gene include four nonsynomous base changes and four splice-site changes that have a detrimental affect on splicing.

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}

     

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