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Rabbit Anti-ZCCHC2  antibody (bs-18550R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-18550R
英文名稱 Rabbit Anti-ZCCHC2  antibody
中文名稱 ZCCHC2蛋白抗體
別    名 9930114B20Rik; AW212015; DKFZp451A185; FLJ20281; KIAA1744; MGC112793; MGC13269; ZCCHC2; ZCHC2_HUMAN; Zinc finger CCHC domain containing protein 2; Zinc finger CCHC domain-containing protein 2.  
研究領域 細胞生物  結合蛋白  鋅指蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Horse)
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 126kDa
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZCCHC2: 101-200/1178 
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 ZCCHC2 is a 1178 amino acid protein that contains one CCHC-type zinc finger, suggesting a role in transcriptional regulation. The gene encoding ZCCHC10 maps to human chromosome 18, which encodes over 300 genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, and erythropoietic protoporphyria. Translocation between chromosome 18 and 14 is also the most common translocation in cancers and occurs in follicular lymphomas.

Similarity:
Contains 1 CCHC-type zinc finger.

SWISS:
Q9C0B9

Gene ID:
54877

Database links:

Entrez Gene: 54877 Human

Entrez Gene: 304695 Rat

SwissProt: Q9C0B9 Human

SwissProt: Q498S6 Rat

Unigene: 114191 Human

Unigene: 714637 Human

Unigene: 225097 Rat



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