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    CMYA2/PDE4DIP Rabbit pAb (bs-9477R)  
    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-9477R
    英文名稱(chēng) CMYA2/PDE4DIP Rabbit pAb
    中文名稱(chēng) 心肌病相關(guān)蛋白2抗體
    別    名 Cardiomyopathy associated protein 2; Cardiomyopathy-associated protein 2; CMYA2; MMGL; MYOME_HUMAN; Myomegalin; Pde4dip; phosphodiesterase 4D interacting protein; phosphodiesterase 4D-interacting protein.  
    研究領(lǐng)域 心血管  信號轉導  細胞骨架  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,Pig,Sheep,Cow,Chicken,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 265 kDa
    檢測分子量
    細胞定位 細胞核 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human CMYA2/PDE4DIP: 1501-1600/2365 
    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 May function as an anchor sequestering components of the cAMP-dependent pathway to Golgi and/or centrosomes. Myomegalin, is a 2,346 amino acid protein that contains one NBPF domain and localizes to the nucleus, cytoplasm, centrosome and Golgi apparatus. Expressed at high levels in fetal and adult heart and at lower levels in brain and placenta, myomegalin is thought to function as an anchoring protein that sequesters members of the cAMP-dependent pathway to the Golgi and to centrosomes, thereby mediating cAMP pathway dynamics. Translocations in the gene that encodes myomegalin are associated with myeloproliferative disorders (MBDs), a group of diseases caused by an overproduction of blood cells. Myomegalin exists as twelve isoforms due to alternative splicing events.

    Function:
    May function as an anchor sequestering components of thecAMP-dependent pathway to Golgi and/or centrosomes (By similarity).

    Subunit:
    Interacts with PDE4D (By similarity).

    Subcellular Location:
    Golgi apparatus (By similarity). Cytoplasm,cytoskeleton, centrosome (By similarity). Cytoplasm. Nucleus.

    Tissue Specificity:
    Highly expressed in heart and skeletal muscle and to a lower extent in brain and placenta.

    DISEASE:
    Note=A chromosomal aberration involving PDE4DIP may bethe cause of a myeloproliferative disorder (MBD) associated witheosinophilia. Translocation t(1;5)(q23;q33) that forms aPDE4DIP-PDGFRB fusion protein.

    Similarity:
    Contains 1 NBPF domain.

    SWISS:
    Q5VU43

    Gene ID:
    9659

    Database links:

    Entrez Gene: 9659 Human

    Entrez Gene: 83679 Mouse

    Entrez Gene: 64183 Rat

    Omim: 608117 Human

    SwissProt: Q5VU43 Human

    SwissProt: Q80YT7 Mouse

    SwissProt: Q9WUJ3 Rat

    Unigene: 584841 Human

    Unigene: 613082 Human

    Unigene: 657490 Human

    Unigene: 728768 Human

    Unigene: 129840 Mouse

    Unigene: 48693 Rat



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