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    TRIM29 (acetyl K116) Rabbit pAb (bs-16731R)  
    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-16731R
    英文名稱(chēng) TRIM29 (acetyl K116) Rabbit pAb
    中文名稱(chēng) 乙?;疶RIM29蛋白抗體
    別    名 Ataxia telangiectasia group D associated protein; Ataxia telangiectasia group D-associated protein; ATDC; FLJ36085; TRI29_HUMAN; TRIM 29; TRIM29; Tripartite motif containing 29; Tripartite motif containing protein 29; Tripartite motif protein 29; Tripartite motif protein TRIM29; Tripartite motif-containing protein 29.  
    產(chǎn)品類(lèi)型 乙?;贵w 
    研究領(lǐng)域 細胞生物  免疫學(xué)  信號轉導  轉錄調節因子  表觀(guān)遺傳學(xué)  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Rabbit,Pig,Cow)
    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 66 kDa
    檢測分子量
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated Synthesised acetylpeptide derived from human TRIM29 around the acetylation site of K116: AK(Ac-K)PP 
    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 The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype. [provided by RefSeq, Jul 2008]

    Function:
    It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell line.

    Subcellular Location:
    Cytoplasm. Colocalizes with intermediate filaments.

    Tissue Specificity:
    Expressed in placenta, prostate and thymus.

    Post-translational modifications:
    Constitutively phosphorylated by PKC on serine/threonine in A431 cells.

    Similarity:
    Contains 1 B box-type zinc finger.

    SWISS:
    Q14134

    Gene ID:
    23650

    Database links:

    Entrez Gene: 23650 Human

    Entrez Gene: 525062 Cow

    Entrez Gene: 72169 Mouse

    Entrez Gene: 300656 Rat

    Omim: 610658 Human

    SwissProt: Q14134 Human

    SwissProt: Q8R2Q0 Mouse

    Unigene: 504115 Human

    Unigene: 273277 Mouse



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