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22号染色体开放阅读框32抗体
  • 产品货号:
    BN40720R
  • 中文名称:
    22号染色体开放阅读框32抗体
  • 英文名称:
    Rabbit anti-C22orf32 Polyclonal antibody
  • 品牌:
    Biorigin
  • 货号

    产品规格

    售价

    备注

  • BN40720R-100ul

    100ul

    ¥2360.00

    交叉反应:Mouse,Rat(predicted:Human,Pig,Cow,Horse,Rabbit,Sheep) 推荐应用:IHC-P

  • BN40720R-200ul

    200ul

    ¥3490.00

    交叉反应:Mouse,Rat(predicted:Human,Pig,Cow,Horse,Rabbit,Sheep) 推荐应用:IHC-P

产品描述

英文名称C22orf32
中文名称22号染色体开放阅读框32抗体
别    名Chromosome 22 open reading frame 32; EMRE_HUMAN; DDDD; dJ186O1.1; mitochondrial; UPF0466 protein C22orf32.  
研究领域细胞生物  免疫学  线粒体  
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Mouse, Rat,  (predicted: Human, Pig, Cow, Horse, Rabbit, Sheep, )
产品应用IHC-P=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量7kDa
细胞定位细胞膜 线粒体
性    状Liquid
浓    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human C22orf32:41-107/107 
亚    型IgG
纯化方法affinity purified by Protein A
储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
产品介绍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.