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    22號染色體開放閱讀框32抗體
    • 產品貨號:
      BN40720R
    • 中文名稱:
      22號染色體開放閱讀框32抗體
    • 英文名稱:
      Rabbit anti-C22orf32 Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN40720R-100ul

      100ul

      ¥2360.00

      交叉反應:Mouse,Rat(predicted:Human,Pig,Cow,Horse,Rabbit,Sheep) 推薦應用:IHC-P

    • BN40720R-200ul

      200ul

      ¥3490.00

      交叉反應:Mouse,Rat(predicted:Human,Pig,Cow,Horse,Rabbit,Sheep) 推薦應用:IHC-P

    產品描述

    英文名稱C22orf32
    中文名稱22號染色體開放閱讀框32抗體
    別    名Chromosome 22 open reading frame 32; EMRE_HUMAN; DDDD; dJ186O1.1; mitochondrial; UPF0466 protein C22orf32.  
    研究領域細胞生物  免疫學  線粒體  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Mouse, Rat,  (predicted: Human, Pig, Cow, Horse, Rabbit, Sheep, )
    產品應用IHC-P=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量7kDa
    細胞定位細胞膜 線粒體
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human C22orf32:41-107/107 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產品介紹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



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


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