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Invitrogen™ MAT1A Polyclonal Antibody
Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5115549
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Description
Antibody detects endogenous levels of total MAT1A.
MAT1A catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
Specifications
| MAT1A | |
| Polyclonal | |
| Unconjugated | |
| MAT1A | |
| AdoMet; AdoMet synthase 1; adoMet synthetase 1; AI046368; Ams; Ams1; Cartilage matrix protein; CMP; CRTM; MAT; MAT 1; Mat1a; MATA1; MAT-I/III; MATN1; matrilin 1, cartilage matrix protein; Matrilin-1; Methionine adenosyltransferase 1; methionine adenosyltransferase 1A; methionine adenosyltransferase I, alpha; methionine adenosyltransferase I/III; S - adenosylmethionine synthetase; SADE; S-adenosylmethionine synthase; S-adenosylmethionine synthase isoform type-1; S-adenosylmethionine synthase isoform type-1; S-adenosylmethionine synthase; S-adenosylmethionine synthetase isoform type-1; SAMS; SAMS1; SAS; similar to S-adenosylmethionine synthetase alpha and beta forms (Methionine adenosyltransferase) (AdoMet synthetase) (MAT-I/III); wu:fi35e01; zgc:55442 | |
| Rabbit | |
| Affinity chromatography | |
| RUO | |
| 11720, 25331, 4143 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide | |
| P13444, Q00266, Q91X83 | |
| MAT1A | |
| A synthesized peptide derived from human MAT1A(Accession Q00266), corresponding to amino acid residues M1-I33. | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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