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環(huán)指蛋白210抗體
  • 產(chǎn)品貨號(hào):
    BN41331R
  • 中文名稱:
    環(huán)指蛋白210抗體
  • 英文名稱:
    Rabbit anti-RNF210 Polyclonal antibody
  • 品牌:
    Biorigin
  • 貨號(hào)

    產(chǎn)品規(guī)格

    售價(jià)

    備注

  • BN41331R-100ul

    100ul

    ¥2360.00

    交叉反應(yīng):Human,Rat(predicted:Mouse,Pig,Horse) 推薦應(yīng)用:WB,IHC-P,IHC-F,IF,ELISA

  • BN41331R-200ul

    200ul

    ¥3490.00

    交叉反應(yīng):Human,Rat(predicted:Mouse,Pig,Horse) 推薦應(yīng)用:WB,IHC-P,IHC-F,IF,ELISA

產(chǎn)品描述

英文名稱RNF210
中文名稱環(huán)指蛋白210抗體
別    名RNF210; Ret finger protein like 4; Ret finger protein-like 4A; RFPL4; RFPL4A; RFPLA_HUMAN; RING finger protein 210.  
研究領(lǐng)域腫瘤  細(xì)胞生物  免疫學(xué)  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應(yīng)Human, Rat,  (predicted: Mouse, Pig, Horse, )
產(chǎn)品應(yīng)用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (石蠟切片需做抗原修復(fù))
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量32kDa
細(xì)胞定位細(xì)胞核 細(xì)胞漿 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human RFPL4A/RNF210:101-200/287 
亞    型IgG
純化方法affinity purified by Protein A
儲(chǔ) 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產(chǎn)品介紹RFPL4A is a 287 amino acid protein. RFPL4A contains a cysteine-rich RING finger-like region (C3YC4), a coiled-coil motif, and B30.2 domains characteristic of the RING-B30 family of E3 ubiquitin-protein ligases, such as MID1. The RFPL4A gene maps to human chromosome 19q13.42. Chromosome 19 consists of approximately 63 million bases and 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 Fc?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.

Similarity:
Contains 1 B30.2/SPRY domain.
Contains 1 RING-type zinc finger.

SWISS:
A6NLU0

Gene ID:
342931

Database links:

Entrez Gene: 342931 Human

Omim: 612601 Human

SwissProt: A6NLU0 Human

Unigene: 631553 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.










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