Arginase 1 (ARG1) Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI4E6]
CAT#: TA502413AM
ARG1 (liver Arginase) mouse monoclonal antibody, clone OTI4E6 (formerly 4E6), Biotinylated
Frequently bought together (3)
Transient overexpression lysate of arginase, liver (ARG1)
USD 436.00
Other products for "Arginase 1"
Specifications
| Product Data | |
| Clone Name | OTI4E6 |
| Applications | FC, IHC, WB |
| Recommended Dilution | WB 1:1000~2000, IHC 1:50, FLOW 1:100 |
| Reactivities | Human, Mouse, Rat |
| Host | Mouse |
| Isotype | IgG1 |
| Clonality | Monoclonal |
| Immunogen | Full length human recombinant protein of human ARG1 (NP_000036) produced in HEK293T cell. |
| Formulation | PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
| Concentration | 0.5 mg/ml |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | Biotin |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Predicted Protein Size | 34.6 kDa |
| Gene Name | arginase 1 |
| Database Link | |
| Background | 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. [provided by RefSeq] |
| Synonyms | arginase; arginase 1; liver; liver-type arginase; OTTHUMP00000017209; type I arginase |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Arginine and proline metabolism, Metabolic pathways |
Documents
| Product Manuals |
| FAQs |
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