FITC标记的22号染色体开放阅读框43抗体-抗体-抗体-生物在线
FITC标记的22号染色体开放阅读框43抗体

FITC标记的22号染色体开放阅读框43抗体

商家询价

产品名称: FITC标记的22号染色体开放阅读框43抗体

英文名称: Anti-C22orf43 /FITC

产品编号: HZ-15140R-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-C22orf43 /FITC Conjugated antibody

FITC标记的22号染色体开放阅读框43抗体

 

英文名称 Anti-C22orf43 /FITC
中文名称 FITC标记的22号染色体开放阅读框43抗体
别    名 C22orf43; Chromosome 22 open reading frame 43; CV043_HUMAN; Putative uncharacterized protein C22orf43; Uncharacterized protein C22orf43.   
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  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Rat, 
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 25kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C22orf43
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:
C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. 

Database links:
UniProtKB/Swiss-Prot: Q6PGQ1.1

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

C22orf43(第22染色体开放阅读框43),又称MGC33025或MGC75009,是由位于人类第22染色体上的基因编码的229个氨基酸蛋白,含有500多个基因和大约4900万个碱基。作为第二个最小的人类染色体,ChoSCOME 22包含多种功能的基因。PelLAN McDeMID综合征,2型神经纤维瘤病和孤独症与22号染色体有关。在22号染色体上发现了一个精神分裂症易感位点,研究表明22q11缺失症状包括精神分裂症的高发病率。染色体9和22之间的易位可能导致费城染色体的形成和随后产生新的融合蛋白BCR-Abl,一种在几种类型的白血病中发现的有效的细胞增殖激活剂。