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    MAMDC2 Rabbit pAb (bs-18641R)  
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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-18641R
    英文名稱 MAMDC2 Rabbit pAb
    中文名稱 MAMDC2蛋白抗體
    別    名 MAM domain-containing protein 2; MAM domain-containing proteoglycan; MAMC2_HUMAN; Mamcan; Mamdc2.  
    研究領域 細胞生物  發育生物學  信號轉導  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Dog,Horse)
    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 75 kDa
    檢測分子量
    細胞定位 細胞外基質 分泌型蛋白 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human MAMDC2: 601-686/686 
    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 MAMDC2 is a 686 amino acid secreted protein that localizes to extracellular matrix. Containing four MAM domains and existing as two alternatively spliced isoforms, MAMDC2 is encoded by a gene located on human chromosome 9q21.11. Chromosome 9 consists of about 145 million bases, 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, Familial dysautonomia and certain leukemias are also associated with chromosome 9.

    Subcellular Location:
    Secreted > extracellular space > extracellular matrix.

    Post-translational modifications:
    O-glycosylated.

    Similarity:
    Contains 4 MAM domains.

    SWISS:
    Q7Z304

    Gene ID:
    256691

    Database links:

    Entrez Gene: 256691 Human

    Omim: 612879 Human

    SwissProt: Q7Z304 Human

    Unigene: 547172 Human



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