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NCCRP1 Rabbit pAb (bs-19046R)  
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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(hào) bs-19046R
英文名稱 NCCRP1 Rabbit pAb
中文名稱 非特異性細(xì)胞毒性受體蛋白1抗體
別    名 Gm163; FBXO50; LOC342897; NCCRP 1; NCCRP1; NCRP1_HUMAN; Non specific cytotoxic cell receptor protein 1 homolog(zebrafish); Non specific cytotoxic cell receptor protein 1 homolog; Non-specific cytotoxic cell receptor protein 1 homolog; Nonspecific cytotoxic cell receptor protein 1 homolog; RGD1305932v.  
研究領(lǐng)域 細(xì)胞生物  轉(zhuǎn)錄調(diào)節(jié)因子  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號(hào)
交叉反應(yīng) (predicted: Human,Mouse,Rat)
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 31 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NCCRP1: 201-275/275 
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 NCCRP1 is a 275 amino acid protein that contains one FBA (F-box associated) domain. The gene encoding NCCRP1 maps to human chromosome 19q13.2. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG families, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Function:
Promotes cell proliferation.

Subcellular Location:
Cytoplasm

Tissue Specificity:
Expressed in the esophagus, oral cavity, skin, tongue and reproductive organs.

Similarity:
Contains 1 FBA (F-box associated) domain.

SWISS:
Q6ZVX7

Gene ID:
342897

Database links:

Entrez Gene: 342897 Human

Entrez Gene: 233038 Mouse

SwissProt: Q6ZVX7 Human

Unigene: 726934 Human



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