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ARG1 Primary Antibody
Item Information | ||
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Catalog # | Size/Concentration | Price |
32008 | 100ug | $358.00 |
Specification | |
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Aliases | ARG1 |
Clone# | 7D1D10 |
Entrez GeneID | 383 |
Formulation | Purified antibody in PBS with 0.05% sodium azide |
Host | Mouse |
Isotype | Mouse IgG1 |
Immunogen | Purified recombinant fragment of human ARG1 (AA: (1-322)) expressed in E. Coli. |
MW | 34.7kDa |
Application | |
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ELISA | 1/10000 |
IHC_P (Immunohistochemistry) | 1/200-1/1000 |
FCM (Flow Cytometry) | 1/200-1/400 |
WB (Western Blot) | 1/500 - 1/2000 |
Sequence |
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AA: 1-322 |
Images
ELISA

Figure 1: Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng)
WESTERN BLOT

Figure 2: Western blot analysis using ARG1 mAb against human ARG1 (AA: (1-322)) recombinant protein. (Expected MW is 38.6 kDa)
WESTERN BLOT

Figure 3: Western blot analysis using ARG1 mAb against HEK293-6e (1) and ARG1 (AA: (1-322))-hIgGFc transfected HEK293-6e (2) cell lysate.
FLOW CYTOMETRY

Figure 4: Flow cytometric analysis of BEL-7402 cells using ARG1 mouse mAb (green) and negative control (red).
FLOW CYTOMETRY

Figure 5: Flow cytometric analysis of Hepg2 cells using ARG1 mouse mAb (green) and negative control (red).
IMMUNOHISTOCHEMISTRY

Figure 6: Immunohistochemical analysis of paraffin-embedded liver cancer tissues using ARG1 mouse mAb with DAB staining.
IMMUNOHISTOCHEMISTRY

Figure 7: Immunohistochemical analysis of paraffin-embedded Stomach cancer tissues using ARG1 mouse mAb with DAB staining.
Product Overview
Description | 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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
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References (references)
References (references) | 1,Medicine (Baltimore). 2020 Aug 7;99(32):e21634.2,Medicine (Baltimore). 2019 Nov;98(47):e17694. |
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