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22號(hào)染色體開(kāi)放閱讀框32抗體
  • 產(chǎn)品貨號(hào)：
    BN40720R
  • 中文名稱：
    22號(hào)染色體開(kāi)放閱讀框32抗體
  • 英文名稱：
    Rabbit anti-C22orf32 Polyclonal antibody
  • 品牌：
    Biorigin

  • 貨號(hào)

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  • BN40720R-100ul

    100ul

    ￥2360.00

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

  • BN40720R-200ul

    200ul

    ￥3490.00

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

產(chǎn)品描述

英文名稱C22orf32
中文名稱22號(hào)染色體開(kāi)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(lǐng)域細(xì)胞生物  免疫學(xué)  線粒體  
抗體來(lái)源Rabbit
克隆類型Polyclonal
交叉反應(yīng)Mouse, Rat,  (predicted: Human, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用IHC-P=1:100-500 （石蠟切片需做抗原修復(fù)）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量7kDa
細(xì)胞定位細(xì)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(chǔ) 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(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



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