ARG1 monoclonal antibody, clone ARG1/1125
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More Files
- More Functions
Western Blot
Western Blot analysis of Lane 1: ARG1 recombinant protein fragment and Lane 2: human liver lysate with ARG1 monoclonal antibody, clone ARG1/1125 (Cat # MAB13324).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human hepatocellular carcinoma with ARG1 monoclonal antibody, clone ARG1/1125 (Cat # MAB13324).
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Specification
Product Description
Mouse monoclonal antibody raised against partial recombinant human ARG1.
Immunogen
Recombinant protein corresponding to 87 residues around amino acids 1-150 of human ARG1.
Host
Mouse
Theoretical MW (kDa)
35-38
Reactivity
Human
Form
Liquid
Purification
Protein A/G purification
Isotype
IgG3, kappa
Recommend Usage
Flow Cytometry (0.5-1 ug/106 cells in 0.1 mL)
Immunofluorescence (1-2 ug/mL)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (2-4 ug/mL)
Western Blot (0.5-1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In 10 mM PBS.
Storage Instruction
Store at -20 to -80°C.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot
Western Blot analysis of Lane 1: ARG1 recombinant protein fragment and Lane 2: human liver lysate with ARG1 monoclonal antibody, clone ARG1/1125 (Cat # MAB13324).Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human hepatocellular carcinoma with ARG1 monoclonal antibody, clone ARG1/1125 (Cat # MAB13324).Immunofluorescence
Flow Cytometry
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Gene Info — ARG1
Entrez GeneID
383Protein Accession#
P05089Gene Name
ARG1
Gene Alias
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Gene Description
arginase, liver
Gene Ontology
HyperlinkGene Summary
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
Other Designations
A-I|OTTHUMP00000017209|arginase, type I
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Interactome
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Pathway
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Disease
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