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    C22orf32 Rabbit pAb (bs-15136R)  
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    產(chǎn)品編號 bs-15136R
    英文名稱(chēng) C22orf32 Rabbit pAb
    中文名稱(chēng) 22號染色體開(kāi)放閱讀框32抗體
    別    名 Chromosome 22 open reading frame 32; CV032_HUMAN; DDDD; dJ186O1.1; mitochondrial; UPF0466 protein C22orf32.  
    研究領(lǐng)域 細胞生物  免疫學(xué)  線(xiàn)粒體  
    抗體來(lái)源 Rabbit
    克隆類(lèi)型 Polyclonal
    克 隆 號
    交叉反應 Human (predicted: Mouse,Rat,Sheep,Cow,Dog,Horse)
    產(chǎn)品應用 WB=1:500-2000
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 7 kDa
    檢測分子量
    細胞定位 細胞膜 線(xiàn)粒體
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human C22orf32: 1-60/107 
    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 Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf32 gene product has been provisionally designated C22orf32 pending further characterization

    Subcellular Location:
    Mitochondrion (Potential). Membrane; Single-pass membrane protein (Potential).

    Similarity:
    Belongs to the UPF0466 family.

    SWISS:
    Q9H4I9

    Gene ID:
    91689

    Database links:

    Entrez Gene: 91689 Human

    SwissProt: Q9H4I9 Human

    Unigene: 306083 Human



    產(chǎn)品圖片
    Sample: Lane 1: Recombinant human C22orf32 protein, N-Trx-His(bs-42185P) Primary: Anti-C22orf32 (bs-15136R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 7 kDa Observed band size: 27 kDa
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