Arginase 1 (ARG1) (NM_000045) Human Recombinant Protein
CAT#: TP721013L
Purified recombinant protein of Human arginase, liver (ARG1)
Need it in bulk or customized? Get a free quote |
CNY 18,030.00
货期*
2周
规格
Product images
经常一起买 (1)
ARG1 (liver Arginase) mouse monoclonal antibody, clone OTI4E6 (formerly 4E6)
CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
Met1-lys322
|
Tag | C-His |
Predicted MW | 35.8 kDa |
Purity | >95% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | Supplied as a 0.2 um filtered solution of 20mM Tris-HCl, 150mM NaCl, 20% Glycerol, 1mM DTT, pH 7.4. |
Storage | Store at < -20°C, stable for 6 months after receipt. Please minimize freeze-thaw cycles. |
Stability | Stable for at least 3 months from date of receipt under proper storage and handling conditions. |
Endotoxin | Endotoxin level is < 0.1 ng/µg of protein (< 1 EU/µg) |
Reference Data | |
RefSeq | NP_000036 |
Locus ID | 383 |
UniProt ID | P05089 |
Refseq Size | 1475 |
Cytogenetics | 6q23.2 |
Refseq ORF | 966 |
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] |
Protein Families | Druggable Genome |
Protein Pathways | Arginine and proline metabolism, Metabolic pathways |
Documents
FAQs |
SDS |
其它Arginase 1产品
Customer
Reviews
Loading...