Recombinatie Arginase-1 monoklonaal antilichaam

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.

Arginase-1

P05089

Human; Mouse; Rat

Recombinant Human Arginase-1 protein

ARGI; ARG; ARG1; arginase-1; A I; Al; ARG 1; ARGI1; Arginase; Arginase 1; Arginase I; Arginase liver; Arginase type I; Arginase1; liver; Liver Arginase; Liver type arginase; Liver-type arginase; Type I arginase; A I; Al; ARG 1; arg1; ARGI1; Arginase 1; Arginase liver; Arginase type I; Arginase; liver; Arginase-1; Arginase1; Liver type arginase; Liver-type arginase; Type I arginase; Arginase; Arginase I

4D1

Unconjugated

WB; IHC

Signal Transduction; Metabolism

Protein A

0.2 mg/mL

IHC 1:200-1:1000; WB 1:2000-1:10000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/CHynv9Cf

35 kDa

35 kDa

IgG, κ