FITC标记的21号染色体开放阅读框59抗体-抗体-抗体-生物在线
FITC标记的21号染色体开放阅读框59抗体

FITC标记的21号染色体开放阅读框59抗体

商家询价

产品名称: FITC标记的21号染色体开放阅读框59抗体

英文名称: Anti-C21orf59/FITC

产品编号: HZ-15126R-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
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  • 所在区域 : 上海
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 Rabbit Anti-C21orf59/FITC Conjugated antibody

FITC标记的21号染色体开放阅读框59抗体

 

英文名称 Anti-C21orf59/FITC
中文名称 FITC标记的21号染色体开放阅读框59抗体
别    名 C21orf48; C21orf59; Chromosome 21 open reading frame 59; CU059_HUMAN; FLJ20467; FLJ37137; FLJ40247; Uncharacterized protein C21orf59.   
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  神经生物学  Alzheimer's  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Pig, Cow, Horse, 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 33kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C21orf59
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:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization. 

Similarity:
To D.melanogaster CG18675.

Database links:
UniProtKB/Swiss-Prot: P57076.1

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

人类染色体中最小的21个构成了人类基因组的1.5%。第21染色体含有近300个基因和4700万个碱基对。唐氏综合征,又称21三体,是最常见的与21号染色体相关的疾病。阿尔茨海默病、Jever和Lange Nielsen综合征和肌萎缩侧索硬化也与第21号染色体有关。在某些白血病中,染色体易位发生在21号染色体和8号染色体之间,以及染色体21和12之间。C21orf59,也称为C21orf48,是一种290个氨基酸的蛋白质,其基因产物暂时命名为C21orf59,有待进一步鉴定。