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Rabbit Anti-CHCHD10  antibody (bs-13888R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-13888R
英文名稱 Rabbit Anti-CHCHD10  antibody
中文名稱 卷曲螺旋結構域蛋白CHCHD10抗體
別    名 C22orf16; CHC10_HUMAN; CHCHD10; Chromosome 22 open reading frame 16; Coiled coil helix coiled coil helix domain containing 10; Coiled coil helix coiled coil helix domain containing protein 10 mitochondrial; Coiled-coil-helix-coiled-coil-helix domain-containing protein 10; MGC70831; mitochondrial; N27C7-4; OTTHUMP00000198408; OTTHUMP00000198409; Protein N27C7-4.  
研究領域 腫瘤  細胞生物  神經生物學  信號轉導  新陳代謝  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Pig,Sheep,Cow)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,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 12.5kDa
細胞定位 細胞漿 線粒體
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CHCHD10: 81-142/142 
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 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. Translo-acations 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 C22orf16 gene product has been provisionally designated CHCHD10 pending further characterization.

Subcellular Location:
Mitochondrion.

Similarity:
Contains 1 CHCH domain.

SWISS:
Q8WYQ3

Gene ID:
400916

Database links:

Entrez Gene: 400916 Human

SwissProt: Q8WYQ3 Human

Unigene: 66915 Human



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