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    MOSPD1 Rabbit pAb (bs-17726R)  
    訂購熱線(xiàn):400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
    技術(shù)支持:techsupport@bioss.com.cn
    50ul/1180.00元
    100ul/1980.00元
    200ul/2800.00元
    大包裝/詢(xún)價(jià)
    產(chǎn)品編號 bs-17726R
    英文名稱(chēng) MOSPD1 Rabbit pAb
    中文名稱(chēng) 精子運動(dòng)結構域蛋白1抗體
    別    名 DJ473B4; MOSPD1; Motile sperm domain containing 1; Motile sperm domain-containing protein 1; MSPD1_HUMAN.  
    研究領(lǐng)域 細胞生物  發(fā)育生物學(xué)  細胞膜蛋白  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Zebrafish,Chicken,Dog,Cat)
    產(chǎn)品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 24 kDa
    檢測分子量
    細胞定位 細胞膜 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human MOSPD1: 51-150/213 
    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(chǎn)品介紹 MOSPD1 is a 213 amino acid multi-pass membrane protein that contains one MSP domain and exists as three alternatively spliced isoforms. The gene encoding MOSPD1 maps to human chromosome Xq26.3. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome

    Subcellular Location:
    Membrane.

    Similarity:
    Contains 1 MSP domain.

    SWISS:
    Q9UJG1

    Gene ID:
    56180

    Database links:

    Entrez Gene: 56180 Human

    Entrez Gene: 70380 Mouse

    Entrez Gene: 317312 Rat

    Omim: 300674 Human

    SwissProt: Q9UJG1 Human

    SwissProt: Q8VEL0 Mouse

    SwissProt: Q5RJS6 Rat

    Unigene: 726077 Human



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