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Liver Arginase 抗体 (ARG1, C-Term)

This anti-Liver Arginase antibody is a 小鼠 单克隆 antibody detecting Liver Arginase in WB, IHC (p) 和 IF. Suitable for 人.
产品编号 ABIN6252586
发货至: 中国

Quick Overview for Liver Arginase 抗体 (ARG1, C-Term) (ABIN6252586)

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), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)

克隆位点

T1ARG-1
  • 抗原表位

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    ARG1, C-Term

    纯化方法

    Protein G affinity chromatography

    免疫原

    A C-terminal recombinant protein fragment from ARG1 was used as the immunogen for the Arginase 1 antibody.

    亚型

    IgG3 kappa
  • 应用备注

    Immunofluorescence: 1-2 μg/mL

    Western blot: 0.5-1 μg/mL

    Immunohistochemistry (FFPE): 2-4 μg/mL for 30 min at RT (1)

    Prediluted format : incubate for 30 min at RT (2)

    Optimal dilution of the Arginase 1 antibody should be determined by the researcher.

    1. Staining of formalin-fixed tissues requires boiling tissue sections in 10  mM Citrate buffer,  pH 6.0, for 10-20 min followed by cooling at RT for 20 min
    2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.2 mg/mL

    缓冲液

    PBS with 0.1 mg/mL BSA and 0.05 % 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

    储存方法

    Aliquot and Store at -20C. Avoid freez-thaw cycles.
  • 抗原

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

    别名

    Arginase 1

    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 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. Two transcript variants encoding different isoforms have been found for this gene. [RefSeq]

    基因ID

    383

    UniProt

    P05089

    途径

    Cellular Response to Molecule of Bacterial Origin
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