Immunology Antibodies 3
Anti-ARG1 Antibody (CAB4923)
- SKU:
- CAB4923
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Immunology
Description
| Antibody Name: | Anti-ARG1 Antibody |
| Antibody SKU: | CAB4923 |
| Antibody Size: | 20uL, 50uL, 100uL |
| Application: | WB IHC IF |
| Reactivity: | Human, Mouse, Rat |
| Host Species: | Rabbit |
| Immunogen: | A synthesized peptide derived from human ARG1 |
| Application: | WB IHC IF |
| Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
| Reactivity: | Human, Mouse, Rat |
| Positive Samples: | Rat liver |
| Immunogen: | A synthesized peptide derived from human ARG1 |
| Purification Method: | Affinity purification |
| Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
| Isotype: | IgG |
| Sequence: | Email for sequence |
| Gene ID: | 383 |
| Uniprot: | P05089 |
| Cellular Location: | Cytoplasm |
| Calculated MW: | 35kDa |
| Observed MW: | 40KDa |
| Synonyms: | ARG1, arginase-1 |
| 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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
| UniProt Protein Function: | ARG1: Homotrimer. By arginine or homoarginine. Belongs to the arginase family. 3 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Amino Acid Metabolism - arginine and proline; EC 3.5.3.1; Hydrolase Chromosomal Location of Human Ortholog: 6q23.2 Cellular Component: cytoplasm; cytosol; extracellular region; nucleus Molecular Function:arginase activity Biological Process: arginine catabolic process; neutrophil degranulation; urea cycle Disease: Argininemia |
| NCBI 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] |
| UniProt Code: | P05089 |
| NCBI GenInfo Identifier: | 12230985 |
| NCBI Gene ID: | 383 |
| NCBI Accession: | P05089.2 |
| UniProt Secondary Accession: | P05089,Q5JWT5, Q5JWT6, Q8TE72, Q9BS50, A6NEA0, |
| UniProt Related Accession: | P05089 |
| Molecular Weight: | 35kDa |
| NCBI Full Name: | Arginase-1 |
| NCBI Synonym Full Names: | arginase 1 |
| NCBI Official Symbol: | ARG1 |
| NCBI Protein Information: | arginase-1 |
| UniProt Protein Name: | Arginase-1 |
| UniProt Synonym Protein Names: | Liver-type arginase; Type I arginase |
| Protein Family: | Arginase |
| UniProt Gene Name: | ARG1 |
 | Western blot - ARG1 Rabbit mAb (CAB4923) |
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