Arginase 1 (ARG1) Mouse Monoclonal Antibody [Clone ID: LBI4E6]
Product Specifications
Background
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]
Synonyms
OTTHUMP00000017209; arginase 1; liver-type arginase; type I arginase; arginase, liver
Gene Name
Homo sapiens arginase 1 (ARG1), transcript variant 2, mRNA.
Gene ID
383
UniProt
P05089
Conjugation
Unconjugated
Related Pathways
Arginine and proline metabolism, Metabolic pathways
Field of Research
Arginine and proline metabolism, Metabolic pathways
Dilution
WB 1:1000~2000, IHC 1:50, FLOW 1:100
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
ARG1
Overview
Carrier-free (BSA/glycerol-free) ARG1 mouse monoclonal antibody, clone LBI4E6
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=383
Uniprot URL
https://www.uniprot.org/uniprot/P05089
Curated Selection
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