Anti - MSH2
英文名称： Anti - MSH2
型号:null    抗体货号： DB 115-RTU-15
价格:请致电：010-57128832,18610462672
品牌: 美国/中国    产品商标: db biotech

上海信裕生物科技有限公司是一家集研发、生产、销售、服务于一体的国际领先生物高新技术企业，专营基因、蛋白、抗体、Elisa试剂盒、细胞生物学，分子生物学等高质量生物产品。抗体纯化/标记/免疫检测：免疫分析检测是一项应用广泛的技术，利用抗原和抗体的特异性反应进行检测的一种手段，广泛用于医学病理学、免疫组织化学、分子生物学、生物制药等领域的分析研究与技术测定。制备高特异性、高效价的抗体是实验免疫学技术的基础，抗体质量的高低将直接影响试验的成败。抗体纯化能降低非特异性本底，抗体标记能通过标记物的增强放大效应提高检测灵敏度，采用ELISA、WB、IP、IHC等不同免疫分析技术检测各种样品中特定的目的蛋白。

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.
CYB5RL,细胞色素B5还原酶样蛋白抗体PubMedPubMed
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. The CYB5RL gene product has been provisionally designated CYB5RL pending further characterization.

Function:
NADH-cytochrome b5 reductases are involved in desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction.

Similarity:
Belongs to the flavoprotein pyridine nucleotide cytochrome reductase family.
Contains 1 FAD-binding FR-type domain.

Gene ID:
606495

Database links:
Entrez Gene: 606495 Human
Entrez Gene: 230582 Mouse
SwissProt: Q6IPT4 Human
SwissProt: B1AS42 Mouse
Unigene: 591426 Human
Unigene: 44608 Mouse

CYB5RL,细胞色素B5还原酶样蛋白抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.