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货号: bs-15308R-PE-Cy7 基本售价: 2980.0 元 规格: 100ul
产品信息
- 产品编号
 - bs-15308R-PE-Cy7
 
- 英文名称
 - Anti-C9orf103/PE-Cy7
 
- 中文名称
 - PE-Cy7标记的9号染色体开放阅读框103抗体
 
- 别 名
 - bA522I20.2; C9orf103; Chromosome 9 open reading frame 103; Glucokinase like protein; Gluconate kinase; Gluconokinase like protein; GNTK_HUMAN; IDNK; OTTHUMP00000021546; OTTHUMP00000021547; Probable gluconokinase; RP11-522I20.2.
 
- 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 信号转导 新陈代谢
 
- 抗体来源
 - Rabbit
 
- 克隆类型
 - Polyclonal
 
- 交叉反应
 - Human, Mouse,
 
- 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
 - 21kDa
 
- 性 状
 - Lyophilized or Liquid
 
- 浓 度
 - 1mg/ml
 
- 免 疫 原
 - KLH conjugated synthetic peptide derived from human C9orf103
 
- 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:
C9orf103 (chromosome 9 open reading frame 103), also known as gluconate kinase, is a 187 amino acid protein that belongs to the gluconokinase gntK/gntV family and catalyzes the conversion of ATP and D-gluconate to ADP and 6-phospho-D-gluconate. Existing as three alternatively spliced isoforms, the gene encoding C9orf103 maps to human chromosome 9q21.32. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Similarity:
Belongs to the gluconokinase GntK/GntV family.
Database links:
UniProtKB/Swiss-Prot: Q5T6J7.1
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

