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ZNFX1 Rabbit pAb (bs-16418R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-16418R
英文名稱 ZNFX1 Rabbit pAb
中文名稱 ZNFX1蛋白抗體
別    名 KIAA1404; NFX1 type zinc finger containing protein 1; RP4-686N3.1404-002; Zinc finger, NFX1-type containing 1.  
研究領(lǐng)域 細(xì)胞生物  轉(zhuǎn)錄調(diào)節(jié)因子  鋅指蛋白  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應(yīng) (predicted: Human,Mouse,Rat,Horse)
產(chǎn)品應(yīng)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 220 kDa
檢測分子量
細(xì)胞定位 細(xì)胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZNFX1: 1601-1700/1918 
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(xiàng) 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 ZNFX1 is a 1918 amino acid nuclear protein that is widely expressed and contains six NF-X1-type zinc fingers, which are presumed to function as zinc binding domains. The gene encoding ZNFX1 maps to human chromosome 20, which contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. There are two isoforms of ZNFX1 that are produced as a result of alternative splicing events.

Function:
ZNFX1 is widely expressed in all tissues. There are two named isoforms.

Tissue Specificity:
Widely expressed.

Similarity:
Contains 6 NF-X1-type zinc fingers.

SWISS:
Q9P2E3

Gene ID:
57169

Database links:

Entrez Gene: 57169 Human

SwissProt: Q9P2E3 Human



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