S-Adenosylmethionine Synthase Isoform Type-1 (MAT1A) Antibody
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Description
S-Adenosylmethionine Synthase Isoform Type-1 (MAT1A) Antibody is a Rabbit polyclonal antibody for the detection of Human S-Adenosylmethionine Synthase Isoform Type-1 (MAT1A).
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | S-Adenosylmethionine Synthase Isoform Type-1 (MAT1A) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Size 1 | 50 µg |
| Size 2 | 100 µg |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
| Availability | Shipped within 5-12 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q00266 |
| Gene ID | 4143 |
| NCBI Accession | NP_000420.1 |
| Background | Antibody anti-MAT1A |
| Status | RUO |
Descripción
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This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency.
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S-Adenosylmethionine Synthase Isoform Type-1 (MAT1A) Antibody
MAT1A Antibody is a Rabbit Polyclonal antibody against MAT1A. This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency.
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