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    MFAP4 Rabbit pAb (bs-18824R)  
    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-18824R
    英文名稱(chēng) MFAP4 Rabbit pAb
    中文名稱(chēng) 微絲相關(guān)蛋白4抗體
    別    名 MFAP4; MFAP4_HUMAN; Microfibril-associated glycoprotein 4; Microfibrillar associated protein 4.  
    研究領(lǐng)域 細胞生物  免疫學(xué)  信號轉導  細胞外基質(zhì)  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Cow,Dog,Horse)
    產(chǎn)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 26 kDa
    檢測分子量
    細胞定位 分泌型蛋白 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human MFAP4: 181-255/255 
    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 This gene encodes a protein with similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

    Function:
    Could be involved in calcium-dependent cell adhesion or intercellular interactions.

    Subcellular Location:
    Secreted; extracellular space; extracellular matrix.

    DISEASE:
    MFAP4 is deleted in the Smith-Magenis syndrome (SMS) [MIM:182290].

    Similarity:
    Contains 1 fibrinogen C-terminal domain.

    SWISS:
    P55083

    Gene ID:
    4239

    Database links:

    Entrez Gene: 4239 Human

    Entrez Gene: 286766 Cow

    Entrez Gene: 489531 Dog

    Entrez Gene: 76293 Mouse

    Entrez Gene: 287382 Rat

    Omim: 600596 Human

    SwissProt: P55918 Cow

    SwissProt: P55083 Human

    SwissProt: Q9D1H9 Mouse

    Unigene: 296049 Human

    Unigene: 272278 Mouse



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