Liver Arginase 抗体
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- 抗原 See all Liver Arginase (ARG1) 抗体
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This Liver Arginase antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
- 产品特性
- Homo sapiens arginase, liver (ARG1)
- 纯化方法
- Purified from mouse ascites fluids by affinity chromatography
- 免疫原
- Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell.
- 克隆位点
- 4E6
- 亚型
- IgG1
- Top Product
- Discover our top product ARG1 Primary Antibody
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- 应用备注
- WB 1:1000~2000, IHC 1:50, FLOW 1:100
- 说明
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The concentration of the product may vary between diferrent lots.
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.5-1.0 mg/mL
- 缓冲液
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
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- 抗原
- Liver Arginase (ARG1) (Arginase, Liver (ARG1))
- 别名
- ARG1 (ARG1 产品)
- 背景
- Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.
- 分子量
- 34.6 kDa
- 基因ID
- 383
- NCBI登录号
- NM_000045
- HGNC
- 383
- 途径
- Cellular Response to Molecule of Bacterial Origin
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