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        FUNDC2 Rabbit pAb (bs-16195R)  
        訂購熱線:400-901-9800
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        訂購QQ:  400-901-9800
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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-16195R
        英文名稱 FUNDC2 Rabbit pAb
        中文名稱 Cervical cancer oncogene 3/宮頸癌原癌基因3抗體
        別    名 Cervical cancer oncogene 3; Cervical cancer proto oncogene 3 protein; DC44; FLJ33773; FUN14 domain containing 2; FUN14 domain containing protein 2; FUNDC 2; HCBP 6; HCBP6; FUND2_HUMAN; HCC 3; HCC3; Hepatitis C virus core binding protein 6; MGC131676; MGC2495; OTTHUMP00000015441; OTTHUMP00000061459; PD03104.  
        研究領域 腫瘤  細胞生物  轉錄調節因子  細菌及病毒  新陳代謝  線粒體  表觀遺傳學  
        抗體來源 Rabbit
        克隆類型 Polyclonal
        克 隆 號
        交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,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 21 kDa
        檢測分子量
        細胞定位 細胞核 細胞漿 線粒體
        性    狀 Liquid
        濃    度 1mg/ml
        免 疫 原 KLH conjugated synthetic peptide derived from human FUNDC2: 101-189/189 
        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 FUNDC2 is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. 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. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as 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.

        Function:
        The function of FUNDC2 (FUN14 domain-containing protein 2) is unknown.

        Subcellular Location:
        Mitochondrial

        Similarity:
        Belongs to the FUN14 family.

        SWISS:
        Q9BWH2

        Gene ID:
        65991

        Database links:

        Entrez Gene: 65991 Human

        Entrez Gene: 67391 Mouse

        SwissProt: Q9BWH2 Human

        SwissProt: Q9D6K8 Mouse

        Unigene: 356050 Human

        Unigene: 126404 Mouse



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