FITC标记的锌指蛋白843抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的锌指蛋白843抗体

FITC标记的锌指蛋白843抗体

商家询价

产品名称: FITC标记的锌指蛋白843抗体

英文名称: Anti-ZNF843/FITC

产品编号: HZ-12225R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-ZNF843/FITC Conjugated antibody

FITC标记的锌指蛋白843抗体

 

英文名称 Anti-ZNF843/FITC
中文名称 FITC标记的锌指蛋白843抗体
别    名 Zinc finger protein 843; ZN843_HUMAN; ZNF843.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  神经生物学  转录调节因子  锌指蛋白  表观遗传学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 37kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from Human ZNF843
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 °C 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°C. 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 °C.
产品介绍 background:
ZNF843 is a 348 amino acid protein that is encoded by a gene which maps to chromosome 16. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The ZNF843 gene product has been provisionally designated MGC46336 pending further characterization.

Similarity:
Contains 2 C2H2-type zinc fingers.

Database links:
Entrez Gene: 283933 Human
SwissProt: Q8N446 Human
Unigene: 722243 Human


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

ZNF843是由一个基因编码的348氨基酸蛋白质,该基因映射到16号染色体。染色体16在大约9千万碱基对中编码900多个基因,占人类细胞DNA的近3%,并且与多种遗传病有关。GAN基因位于16号染色体上,随着突变,可能导致巨大的轴突神经病变,一种神经系统紊乱,特征是随着生长而增加功能障碍。罕见的Rubinstein-Taybi综合征也通过编码关键CREB结合蛋白的CREBBP基因与16号染色体相关。Rubinstein Taybi的症状包括精神发育迟滞和肿瘤生长和白细胞肿瘤的易感性。Crohn病是通过NOD2基因与16号染色体相关的胃肠道炎症状态。系统性红斑狼疮和许多其它与染色体16的着丝粒周区相关的自身免疫性疾病导致SLC5A11被鉴定为潜在的自身免疫调节剂。ZNF843基因产物已暂时指定为MGC46336,有待进一步鉴定。