FITC标记的EMID1蛋白抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的EMID1蛋白抗体

FITC标记的EMID1蛋白抗体

商家询价

产品名称: FITC标记的EMID1蛋白抗体

英文名称: Anti-EMID1/FITC

产品编号: HZ-14581R-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 点击查看
  • 传真 : 点击查看
  • 邮箱 : www.shzbio.net
  • 二维码 : 点击查看

 Rabbit Anti-EMID1/FITC Conjugated antibody

FITC标记的EMID1蛋白抗体

 

英文名称 Anti-EMID1/FITC
中文名称 FITC标记的EMID1蛋白抗体
别    名 AW122071; CO 5; CTA-984G1.2; EMI domain containing 1; EMI domain containing protein 1; EMI domain-containing protein 1; EMI5; EMID 1; Emid1; EMID1_HUMAN; Emilin and multimerin domain containing protein 1; Emilin and multimerin domain-containing protein 1; EMU1; hEmu1; MGC50657; OTTMUSP00000005297; Protein Emu1; Putative emu1; RGD1565846; RP23-338J18.3.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  神经生物学  信号转导  细胞类型标志物  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Cow, 
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 43kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human EMID1
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:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. 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.

Subunit:
Homo- or heteromers.

Subcellular Location:
Secreted; extracellular space; extracellular matrix.

Similarity:
Contains 1 collagen-like domain.
Contains 1 EMI domain.

Database links:

Entrez Gene: 129080 Human

Entrez Gene: 140703 Mouse

Entrez Gene: 685462 Rat

Omim: 608926 Human

SwissProt: Q96A84 Human

SwissProt: Q91VF5 Mouse

Unigene: 289106 Human

Unigene: 840 Mouse

Unigene: 81507 Rat



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

22号染色体含有500个以上的基因和4900万个碱基。作为第二个最小的人类染色体,22包含令人惊讶的各种有趣的基因。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。