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Liver Arginase 抗体

This anti-Liver Arginase antibody is a 小鼠 单克隆 antibody detecting Liver Arginase in WB, ELISA, FACS 和 IHC (p). Suitable for 人.
产品编号 ABIN7464600
发货至: 中国

Quick Overview for Liver Arginase 抗体 (ABIN7464600)

抗原

See all Liver Arginase (ARG1) 抗体
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

适用

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宿主

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小鼠

克隆类型

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单克隆

标记

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This Liver Arginase antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

GT5811
  • 特异性

    This antibody is specific for human Arginase 1 protein, and it does not cross react with human Arginase 2 protein.

    交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Affinity purified by Protein A.

    免疫原

    Full length human Arginase 1 recombinant protein.

    亚型

    IgG2a
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. FACS: 1:50-1:200. ELISA: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: Huh-7 , ARG1-transfected 293T

    Validation: Overexpression

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    3.26 mg/mL

    缓冲液

    PBS, No Preservative

    储存液

    Without preservative

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Liver Arginase (ARG1) (Arginase, Liver (ARG1))

    别名

    arginase 1

    背景

    Arginase 1,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. [provided by RefSeq]

    分子量

    35 kDa

    基因ID

    383

    UniProt

    P05089

    途径

    Cellular Response to Molecule of Bacterial Origin
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