catalog number :
MBS179560
products full name :
Anti-ARG1/Arginase 1 Rabbit Monoclonal Antibody
products short name :
[ARG1/Arginase 1]
products name syn :
[Arginase-1; 3.5.3.1; Liver-type arginase; Type I arginase; ARG1]
other names :
[arginase-1 isoform 2; Arginase-1; arginase-1; arginase 1; Liver-type arginase; Type I arginase]
products gene name :
[ARG1]
other gene names :
[ARG1; ARG1]
reactivity :
Human, Mouse, Rat
purity :
Affinity-chromatography
form :
Liquid; Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
concentration :
0.5-1mg/ml, actual concentration vary by lot. Use suggested dilution ratio to decide dilution procedure.
storage stability :
Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
tested application :
Immunoprecipitation (IP), Western Blot (WB)
app notes :
WB: 1:500-1:2000. IP: 1:50
image1 heading :
Immunohistochemistry (IHC)
image2 heading :
Western Blot (WB)
other info1 :
Immunogen: A synthesized peptide derived from human ARG1. Conjugate: No
products categories :
Neuroscience; Neurology Process; neuroendocrinology; gh regulation; Biochemicals; Product Range; just add water; Chemical Type; bioactive peptides; Pharmacology; Receptors & transporters; peptide Receptors; ghrelin; agonists
products description :
Anti-ARG1 Rabbit Monoclonal Antibody tested for IP, WB in Human, Mouse, Rat
ncbi acc num :
NP_000036.2
ncbi gb acc num :
NM_000045.3
ncbi pathways :
ATF-2 Transcription Factor Network Pathway (138006); Amoebiasis Pathway (167324); Amoebiasis Pathway (167191); Arginine And Proline Metabolism Pathway (82957); Arginine And Proline Metabolism Pathway (323); Biosynthesis Of Amino Acids Pathway (790012); Biosynthesis Of Amino Acids Pathway (795174); IL4-mediated Signaling Events Pathway (137933); Metabolism Pathway (477135); Metabolism Of Amino Acids And Derivatives Pathway (106169)
ncbi 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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
uniprot summary :
Key element of the urea cycle converting L-arginine to urea and L-ornithine, which is further metabolized into metabolites proline and polyamides that drive collagen synthesis and bioenergetic pathways critical for cell proliferation, respectively; the urea cycle takes place primarily in the liver and, to a lesser extent, in the kidneys.
size3 :
0.1 mg + Biotin Secondary (MBS176645)
size4 :
0.1 mg + HRP Secondary (MBS176703)