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Arginase 1 Monoclonal Antibody (sl6arg), eFluor™ 660, eBioscience™, Invitrogen™

Mouse Monoclonal Antibody

£168.00 - £403.00

Specifications

Antigen Arginase 1
Clone sl6arg
Concentration 0.2 mg/mL
Applications Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Classification Monoclonal
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Products 2
Product Code Brand Quantity Price Quantity & Availability  
Product Code Brand Quantity Price Quantity & Availability  
15540137
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Affymetrix eBioscience
50-9779-80
25 μg
£168.00
25µg
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Estimated Shipment: 06-06-2024
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15550137
View Documents Promotion Details
Affymetrix eBioscience
50-9779-82
100 μg
£403.00
100µg
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Estimated Shipment: 06-06-2024
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Description

Description

Arginase-1 (ARG1) catalyzes the hydrolysis of L-arginine into ornithine and urea, a critical step for the urea cycle. Defects in ARG1 are the cause of argininemia, an autosomal recessive disorder characterized by hyperammonemia. There are several isoforms of mammalian arginase. The type I isoform, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Hepatocellular carcinoma usually shows higher protein expression of ARG1 than normal liver cells.

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.
Specifications

Specifications

Arginase 1
0.2 mg/mL
Monoclonal
Liquid
RUO
PBS with 0.09% sodium azide; pH 7.2
AI; A-I; AI type I arginase; AI256583; Arg1; Arg-1; Arginase; arginase 1; arginase 1 liver; arginase 1, liver; arginase I; arginase, liver; Arginase1; arginase-1; HGNC:663; Liver Arginase; Liver-type arginase; PGIF; similar to arginase, type I; Type 1 Arginase; type I arginase
ARG1
Primary
4° C, store in dark, DO NOT FREEZE!
ARG1
sl6arg
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
eFluor 660
Mouse
Human
P05089
383
IgG1 κ
Affinity chromatography
Antibody
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