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γ谷氨酰半胱氨酸合成酶抗体

γ谷氨酰半胱氨酸合成酶抗体
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  • 产品名称:γ谷氨酰半胱氨酸合成酶抗体
  • 产品型号: GCLC
  • 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
γ谷氨酰半胱氨酸合成酶抗体应用于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。γ谷氨酰半胱氨酸合成酶抗体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。
产品描述

γ谷氨酰半胱氨酸合成酶抗体

规格:1mg/1ml

英文名: GCLC

别名: Gamma ECS; Gamma GCS; Gamma glutamylcysteine synthetase; Gamma-ECS; Gamma-glutamylcysteine synthetase; GCL; GCLC; GCLM; GCS; GCS Heavy Chain antibody GLCL; GLCLC; GLCLR; Glutamate cysteine ligase cata

分子量: 73kDa

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 GCLC

交叉反应:Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit,

细胞定位:细胞浆

γ谷氨酰半胱氨酸合成酶抗体产品介绍:background: The GCLC gene consists of 16 exons and encodes the 636 amino acid protein g-GCSc (g-glutamylcysteine synthetase heavy subunit), also designated g-L-glutamate-L-cysteine ligase catalytic subunit (GLCLC). g-GCSc is expressed in hemocytes, brain, liver and kidney. g-GCSc associates with a regulatory or modifier subunit, g-GCSm (g-glutamylcysteine synthetase light subunit), to form a heterodimer, g-GCS. g-GCS is the first enzyme involved and the rate determining step in glutathione biosynthesis. Oxidants, cadium and methyl mercury upregulate the transcription of g-GCS. H2O2 regulation depends on the Yap1 protein and the presence of glutamate, glutamine and lysine. Cadium regulates transcription through proteins Met-4, Met-31 and Met-32. Cbf1, a DNA binding protein, inhibits transcription of g-GCS. Chemopreventive compounds cause increased levels of g-GCSc in kidney tissues, which may protect against γ谷氨酰半胱氨酸合成酶抗体chemically induced carcinogenesis. A His370Leu amino acid change in g-GCSc causes deficiencies in activity which are responsible for hemolytic anemia and low red blood cell glutathione levels. Defects in GCLC are the cause of hemolytic anemia. Subunit: Heterodimer of a catalytic heavy chain and a regulatory light chain. DISEASE: Defects in GCLC are the cause of hemolytic anemia (HAGGSD) [MIM:230450]. Similarity: Belongs to the glutamate--cysteine ligase type 3 family. Database links: Entrez Gene: 2729 Human Entrez Gene: 14629 γ谷氨酰半胱氨酸合成酶抗体Mouse Entrez Gene: 25283 Rat Omim: 606857 Human SwissProt: P48506 Human SwissProt: P97494 Mouse SwissProt: P19468 Rat Unigene: 654465 Human Unigene: 89888 Mouse Unigene: 8365 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

γ谷氨酰半胱氨酸合成酶抗体品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (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:肿瘤  细胞生物  **学  神经生物学  信号转导  

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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