Anti-RNF210/FITC Conjugated抗体-抗体-抗体-生物在线
上海沪震实业有限公司
Anti-RNF210/FITC Conjugated抗体

Anti-RNF210/FITC Conjugated抗体

商家询价

产品名称: Anti-RNF210/FITC Conjugated抗体

英文名称: Anti-RNF210/FITC

产品编号: YB--8494R-FITC

产品价格: null

产品产地: 中国/美国

品牌商标: Ybscience

更新时间: 2023-08-17T10:24:20

使用范围: 科研使用

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 Anti-RNF210/FITC Conjugated抗体

品编号 YB-8494R-FITC
英文名称 Anti-RNF210/FITC
中文名称 FITC标记的环指蛋白210抗体
别    名 RNF210; Ret finger protein like 4; Ret finger protein-like 4A; RFPL4; RFPL4A; RFPLA_HUMAN; RING finger protein 210.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Pig, Horse, 
产品应用 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 32kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RFPL4A/RNF210
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 癈 for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20癈. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 癈.
产品介绍 background:
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. 

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.