Human Recombinant Arginase 1 (from E. coli)
75791-004
: Prosci
:
- Enzyme type:Recombinant
- Source:E. coli
- Species:Human
- Size:0.05 mg
- Tag sequence:C-6 His tag
- Storage conditions:Lyophilized protein should be stored at –20 °C, though stable at room temperature for 3 weeks. Reconstituted protein solution can be stored at 4...7 °C for 2 - 7 days. Aliquots of reconstituted samples are stable at –20 °C for 3 months.
- Endotoxin content:<0.1 ng/ug (1 IEU/ug) as determined by LAL test.
- Enzyme name:Arginase 1
- Enzyme synonyms:Arginase-1, Liver-type arginase, Type I arginase, ARG1
- Purity:>95% as determined by reducing SDS-PAGE
- Molecular weight:35.8 kD
- Sequence:Met1-lys322
- Formulation:Lyophilized from a 0.2 µm filtered solution of 20 mM TrisHCl, pH 7.5 . Always centrifuge tubes before opening. Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100 ug/ml. Dissolve the Lyophilized protein in ddH2O. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
- Tested applications:Biological assays
- Cat. no.:75791-004
- Supplier No.:92-205
ARG1 is a member of the ureohydrolase family of enzymes
This recombinant protein can be used for biological assays. For research use only.
Fusion-Tag: C-6 His tag
ARG1 can catalyze the hydrolysis of arginine to ornithine and urea. In the urea cycle, ARG1 catalyzes the fifth and final step, a series of biochemical reactions in mammals during which the body disposes of harmful ammonia. ARG1 is a cytosolic enzyme and expressed widely in the liver as part of the urea cycle. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterized by hyperammonemia.