FITC标记的KLHDC4蛋白抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的KLHDC4蛋白抗体

FITC标记的KLHDC4蛋白抗体

商家询价

产品名称: FITC标记的KLHDC4蛋白抗体

英文名称: Anti-KLHDC4/FITC

产品编号: HZ-16760R-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-KLHDC4/FITC Conjugated antibody

FITC标记的KLHDC4蛋白抗体

 

英文名称 Anti-KLHDC4/FITC
中文名称 FITC标记的KLHDC4蛋白抗体
别    名 DKFZp434G0522; FLJ00104; Kelch domain containing protein 4. KLDC4_HUMAN   
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  免疫学  发育生物学  转录调节因子  表观遗传学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Horse, 
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 58kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human KLHDC4
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:
KLHDC4 is a 520 amino acid protein that contains six kelch repeats and exists as three alternatively spliced isoforms. The gene encoding KLHDC4 maps to human chromosome 16q24.2 and mouse chromosome 8 E1. 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.

Function:
Kelch proteins (and Kelch-like proteins) are proteins that have repeated kelch domains. Most Kelch proteins also have a BTB (defn) domain. Each kelch domain forms the blade of a propellar structure, with the repeated kelch domains forming a Beta-propellar. The structure of this Beta-propellar is known but the function is not characterised. KLHDC4 contains six Kelch repeats. There are three named isoforms.

Similarity:
Contains 6 Kelch repeats.

Database links:

Entrez Gene: 54758 Human

SwissProt: Q8TBB5 Human



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

KLHDC4是包含六个KelCH重复序列的520个氨基酸的蛋白质,存在三个交替剪接的异构体。编码KLHDC4的基因定位于人类染色体16q24.2和小鼠染色体8 E1。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。