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8-羟基鸟嘌呤DNA糖基化酶

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产品名称: 8-羟基鸟嘌呤DNA糖基化酶
产品型号: OGG1
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

8-羟基鸟嘌呤DNA糖基化酶应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。8-羟基鸟嘌呤DNA糖基化酶生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


8-羟基鸟嘌呤DNA糖基化酶  的详细介绍

8-羟基鸟嘌呤DNA糖基化酶

规格:1mg/1ml

英文名: OGG1

别名: 8 hydroxyguanine DNA glycosylase; 8 oxoguanine DNA glycosylase 1; 8-oxoguanine DNA glycosylase; AP lyase; DNA apurinic or apyrimidinic site lyase; DNA lyase; DNA-(apurinic or apyrimidinic site) lyase;

分子量: 38-47kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human OGG1/8 h

交叉反应:Human, Mouse, Rat, Dog, Pig, Cow,

细胞定位:

8-羟基鸟嘌呤DNA糖基化酶产品介绍:background: This gene encodes the enzyme responsible for the excision of 8-oxoguanine, a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen. The action of this enzyme includes lyase activity for chain cleavage. Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups, type 1 and type 2, depending on the last exon of the sequence. Type 1 alternative splice variants end with exon 7 and type 2 end with exon 8. All variants share the N-terminal region in common, which contains a mitochondrial targeting signal that is essential for mitochondrial localization. Many alternative splice variants for this gene have been described, but the full-length nature for every variant has not been determined. [provided by RefSeq, Aug 2008]. Function: DNA repair enzyme that incises DNA at 8-oxoG residues. Excises 7,8-dihydro-8-oxoguanine and 2,6-diamino-4-hydroxy-5-N-methylformamidopyrimidine (FAPY) from damaged DNA. Has a beta-lyase activity that nicks DNA 3' to the lesion. Subcellular Location: Mitochondrion; Nucleus and Nucleus > nucleoplasm. Nucleus speckle. Nucleus matrix. Together with APEX1 is recruited to nuclear speckles in UVA-irradiated cells. Tissue Specificity8-羟基鸟嘌呤DNA糖基化酶: Ubiquitous. DISEASE: Defects in OGG1 may be a cause of renal cell carcinoma (RCC) [MIM:144700]. It is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium. It is subclassified into clear cell renal carcinoma (non-papillary carcinoma), papillary renal cell carcinoma, chromophobe renal cell carcinoma, collecting duct carcinoma with 8-羟基鸟嘌呤DNA糖基化酶medullary carcinoma of the kidney, and unclassified renal cell carcinoma. Similarity: Belongs to the type-1 OGG1 family. Database links: Entrez Gene: 4968 Human Entrez Gene: 18294 Mouse Omim: 601982 Human SwissProt: O15527 Human SwissProt: O08760 Mouse Unigene: 380271 Human Unigene: 43612 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

8-羟基鸟嘌呤DNA糖基化酶产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  **学  染色质和核信号  线粒体  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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