Anti-IQCC/FITC Conjugated抗体-抗体-抗体-生物在线
上海沪震实业有限公司
Anti-IQCC/FITC Conjugated抗体

Anti-IQCC/FITC Conjugated抗体

商家询价

产品名称: Anti-IQCC/FITC Conjugated抗体

英文名称: Anti-IQCC/FITC

产品编号: YB--9019R-FITC

产品价格: null

产品产地: 中国/美国

品牌商标: Ybscience

更新时间: 2023-08-17T10:24:20

使用范围: 科研使用

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 Anti-IQCC/FITC Conjugated抗体

产品编号 YB-9019R-FITC
英文名称 Anti-IQCC/FITC
中文名称 FITC标记的IQCC蛋白抗体
别    名 IQ domain containing protein C; IQ domain-containing protein C; IQ motif containing C; Iqcc; IQCC_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, Pig, Horse, 
产品应用 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 53kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human IQCC
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 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Similarity:
Contains 1 IQ domain.

Database links:

Entrez Gene: 55721 Human

Entrez Gene: 230767 Mouse

SwissProt: Q4KMZ1 Human

SwissProt: A2ADZ8 Mouse

Unigene: 274356 Human

Unigene: 441132 Mouse



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