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Anti-ARG1 Antibody EPR6671(B)
Also for ARG1 (NM_000045)
|A synthetic peptide corresponding to residues in human ARG1 was used as an immunogen.|
|Human, Mouse, Rat
||Lot dependent; please refer to CoA along with shipment
||WB: 1:1000 - 1:10000; IP: 1:10 - 1:100
|PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%|
|Tissue culture supernatant
|Is unsuitable for ICC/IF or IHC-P.
|Homo sapiens arginase 1 (ARG1), transcript variant 2|
|OTTHUMP00000017209; arginase 1; liver-type arginase; type I arginase; arginase, liver|
|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 ARG1 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 (1).|
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Western blot - Anti-liver Arginase antibody [EPR6671(B)]; All lanes : Anti-liver Arginase antibody [EPR6671(B)] at 1/1000 dilution.Lane 1 : Fetal liver lysate.Lane 2 : Mouse liver lysate.Lysates/proteins at 10 µg per lane.Secondary.HRP labelled goat anti-rabbit at 1/2000 dilution.Predicted band size : 35 kDa.