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ZC3H3 Rabbit pAb (bs-18465R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
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產(chǎn)品編號 bs-18465R
英文名稱 ZC3H3 Rabbit pAb
中文名稱 ZC3H3蛋白抗體
別    名 KIAA0150; ZC3H3; ZC3H3_HUMAN; ZC3HDC3; Zinc finger CCCH domain containing protein 3; Zinc finger CCCH domain-containing protein 3; Zinc finger CCCH type containing 3; Zinc finger CCCH type domain containing 3.  
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
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Horse)
產(chǎn)品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/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 103 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZC3H3: 851-948/948 
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(chǎn)品介紹 ZC3HDC3 is a 948 amino acid protein that contains five C3H1-type zinc finger domains. ZC3HDC3 plays a regulatory role in nuclear adenylation and export. Two isoforms of ZC3H13 exists as a result of alternative splicing events. The gene encoding ZC3H13 maps to chromosome 8, which encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects.

Similarity:
Contains 5 C3H1-type zinc fingers.

SWISS:
Q8IXZ2

Gene ID:
23144

Database links:

Entrez Gene: 23144 Human

SwissProt: Q8IXZ2 Human

Unigene: 521915 Human



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