FITC标记的2号染色体开放阅读框50抗体-抗体-抗体-生物在线
FITC标记的2号染色体开放阅读框50抗体

FITC标记的2号染色体开放阅读框50抗体

商家询价

产品名称: FITC标记的2号染色体开放阅读框50抗体

英文名称: Anti-C2orf50/FITC

产品编号: HZ-15151R-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

上海沪震实业有限公司
  • 联系人 : 鲍丽雯
  • 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 139****0749
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  • 邮箱 : www.shzbio.net

 Rabbit Anti-C2orf50/FITC Conjugated antibody

FITC标记的2号染色体开放阅读框50抗体

 

英文名称 Anti-C2orf50/FITC
中文名称 FITC标记的2号染色体开放阅读框50抗体
别    名 C2orf50; CB050_HUMAN; Chromosome 2 open reading frame 50; FLJ25143; Hypothetical protein LOC130813; MGC149401; Uncharacterized protein C2orf50.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 细胞生物  免疫学  
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 18kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C2orf50
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:
C2orf50 (chromosome 2 open reading frame 50), also known as FLJ25143 or MGC149401, is a 162 amino acid protein that is encoded by a gene located on human chromosome 2p25.1. The second largest human chromosome, chromosome 2 consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

Database links:
UniProtKB/Swiss-Prot: Q96LR7.1

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

C2orf50(染色体2开放阅读框50),也称为FLJ25143或MGC149401,是由位于人类染色体2p25.1上的基因编码的162个氨基酸蛋白。人类第二大染色体2号染色体由2.37亿个碱基组成,编码1400多个基因,约占人类基因组的8%。许多遗传疾病与2号染色体上的基因有关。丑角鳞癣,一种罕见的病态皮肤畸形,与ABCA12基因突变有关。脂类代谢紊乱是与ABCG5和ABCG8相关的。ALSTR综合征是一种极为罕见的隐性遗传性疾病,其原因在于ALMS1基因的突变。有趣的是,染色体2包含看起来是残留的第二着丝粒和残留端粒,这证实了人类染色体2是今天在猿类中以现代形式出现的两个祖先染色体的古老融合的结果。