Home  >  Products  >  ARG2, aa23-354, Recombinant, Human (Arginase, Type II, Arginase-2, Mitochondrial, Kidney-type Arginase, Non-hepatic Arginase, Type II Arginase)

ARG2, aa23-354, Recombinant, Human (Arginase, Type II, Arginase-2, Mitochondrial, Kidney-type Arginase, Non-hepatic Arginase, Type II Arginase)

Cat no: A3340-17H


Supplier: United States Biological
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Arginase is a manganese-containing enzyme which catalyzes the hydrolysis of arginine to ornithine and urea. It is the final enzyme of the urea cycle. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic cross-reactivity and physiologic function. The type II isoform is located in the mitochondria and expressed in extra-hepatic tissues, especially kidney. It is thought to play a role in nitric oxide and polyamine metabolism. Recombinant protein corresponding to aa23-354 of human ARG2 fused to a His-tag at the N-terminal expressed in E. coli (NP_001163). AA Sequences: MGSSHHHHHH SSGLVPRGSH MVHSVAVIGA PFSQGQKRKG VEHGPAAIRE AGLMKRLSSL GCHLKDFGDL SFTPVPKDDL YNNLIVNPRS VGLANQELAE VVSRAVSDGY SCVTLGGDHS LAIGTISGHA RHCPDLCVVW VDAHADINTP LTTSSGNLHG QPVSFLLREL QDKVPQLPGF SWIKPCISSA SIVYIGLRDV DPPEHFILKN YDIQYFSMRD IDRLGIQKVM ERTFDLLIGK RQRPIHLSFD IDAFDPTLAP ATFTPVVGGL TYREGMYIAE EIHNTGLLSA LDLVEVNPQL ATSEEEAKTT ANLAVDVIAS SFGQTREGGH IVYDQLPTPS SPDESENQAR VRI Molecular Weight: 38.3kD (353aa), confirmed by MALDI-TOF Storage and Stability: May be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing.. Store at -20 degrees C. Aliquots are stable for 6 months at -20 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Catalogue number: A3340-17H
Size: 50ug
Form: Supplied as a liquid in 20mM Tris-HCl, pH 8.0, 10% glycerol.
Purity: ~95% by SDS-PAGE. Purified using conventional chromatography techniques.
References: 1. Frumento G., et al. (2008) Int J Cancer. 123(5):1108-16. 2. J Meurs H., et al. (2010) Pharmacogenet Genomics. 20(3):179-86.

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