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  • Arginase 1 Antibodies

AbboMax

ARG1 Polyclonal Antibody

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Protocols
Questions & Answers

Cite ARG1 Polyclonal Antibody

  • Antibody Testing Data (1)
ARG1 Antibody in Western Blot (WB)
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ARG1 Antibody in Western Blot (WB)
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ARG1 Antibody (600-490) in WB

Western Blot: The recombinant protein Arginase (20 µg/lane) immunoblotted by Rabbit anti – Arginase (Cat# 500-490) at 1:500. Observed a major immunoreactive band at molecular weight ~35 kDa. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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ARG1 Antibody in Western Blot (WB)

Product Details

600-490

Applications
Tested Dilution
Publications

Western Blot (WB)

0.1-1 µg/mL
-

ELISA (ELISA)

0.01-0.1 µg/mL
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Arginase ARG1

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.5 mg/mL

Purification

Antigen affinity chromatography

Storage buffer

PBS with proprietary stabilizer

Contains

0.01% sodium azide

Storage conditions

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Shipping conditions

Wet ice

Product Specific Information

Positive control: Liver tissue

Cellular location: Cytoplasm.

Target Information

Arginase-1 (Arg1) is a 35 kDa enzyme converting L-arginine to urea and L-ornithine, which is the final step in the urea cycle. The resulting polyamines are important for cell proliferation and removal of toxins that arise from protein degradation. By degrading arginine, Arginase 1 deprives NO synthase of its substrate and down-regulates nitric oxide production. In both human and mouse, Arginase 1 is expressed in the liver, neutrophils, myeloid derived suppressor cells (MDSC) and neural stem cells. In human, expression in blood neutrophils but not in CCR3+ granulocytes has been reported. In mice, expression of Arginase 1 is one of the hallmarks of alternatively activated macrophages (M2a). Arginase-1 may be expressed in the myeloid cells infiltrating tumors, and is typically found in the majority of hepatocellular carcinomas. Defects in Arginase 1 are the cause of argininemia, an autosomal recessive disorder characterized by hyperammonemia.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: A-I; Arginase; arginase 1 liver; arginase, liver; Arginase-1; Arginase1; HGNC:663; Liver Arginase; Liver-type arginase; Type 1 Arginase; Type I arginase

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Gene Aliases: ARG1

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UniProt ID: (Human) P05089

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Entrez Gene ID: (Human) 383

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Function(s)
arginase activity manganese ion binding
Process(es)
urea cycle liver development positive regulation of endothelial cell proliferation arginine catabolic process aging response to herbicide response to manganese ion response to zinc ion response to selenium ion regulation of L-arginine import response to amine arginine catabolic process to ornithine lung development collagen biosynthetic process response to vitamin A response to vitamin E response to drug response to amino acid response to cadmium ion response to axon injury response to methylmercury mammary gland involution maternal process involved in female pregnancy protein homotrimerization cellular response to hydrogen peroxide cellular response to lipopolysaccharide cellular response to interleukin-4 cellular response to glucagon stimulus cellular response to dexamethasone stimulus cellular response to transforming growth factor beta stimulus
It has to be done as per old AB suggested Products section.
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