FITC标记的2号染色体开放阅读框61抗体-抗体-抗体-生物在线
FITC标记的2号染色体开放阅读框61抗体

FITC标记的2号染色体开放阅读框61抗体

商家询价

产品名称: FITC标记的2号染色体开放阅读框61抗体

英文名称: Anti-C2orf61/FITC

产品编号: HZ-15155R-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
  • 传真 : 021-60345367
  • 邮箱 : www.shzbio.net

 Rabbit Anti-C2orf61/FITC Conjugated antibody 

FITC标记的2号染色体开放阅读框61抗体

 

英文名称 Anti-C2orf61/FITC
中文名称 FITC标记的2号染色体开放阅读框61抗体
别    名 CCDC113; Chromosome 2 open reading frame 61; Coiled-coil domain-containing protein 113 Gene names; DKFZp434N1418; HSPC065; Uncharacterized protein C2orf61; CB061_HUMAN.  
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, Mouse, Rat, Dog, Cow, Rabbit, Sheep, 
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 19kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C2orf61
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:
C2orf61 (chromosome 2 open reading frame 61), also known as FLJ40172, is a 177 amino acid protein encoded by a gene that maps to human chromosome 2p21. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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 related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Database links:
UniProtKB/Swiss-Prot: Q8N801.1

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

C2orf61(2号染色体开放阅读框61),也称为FLJ40172,是由一个基因编码的177个氨基酸蛋白,该基因与人类2号染色体2p21定位。染色体2作为人类第二大染色体,约占人类基因组的8%,包含2.37亿个编码1400多个基因的碱基。许多遗传疾病与2号染色体上的基因有关。HARKQUIN是一种罕见的皮肤畸形,与ABCA12基因的突变有关。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,与ALMS1基因突变有关。染色体2包含一个可能的残留第二着丝粒以及残留端粒,这证实了人类染色体2是由两个祖先染色体的古老融合形成的假说,这两个祖先染色体仍然存在于现代猿类中。