Thermo Fisher Scientific MAT1A Polyclonal Antibody
Thermo Fisher Scientific의 MAT1A 폴리클로날 항체는 인간, 마우스, 랫트에 반응하며 WB 및 IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제된 고품질 항체로, 4°C 또는 -20°C에서 안정적으로 보관 가능합니다. 연구용으로만 사용됩니다.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:3,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:100–1:1,000 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein encompassing a sequence within the center region of human MAT1A (exact sequence proprietary) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1.66 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage buffer | PBS, pH 7, with 20% glycerol |
| Contains | 0.025% ProClin 300 |
| Storage conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping conditions | Wet ice |
| RRID | AB_2736118 |
Product Specific Information
- Positive Control: Mouse liver
- Predicted Reactivity: Human (100%), Pig (95%), Chicken (85%), Bovine (91%)
- Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
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 persistent hypermethioninemia.
This gene 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 persistent hypermethioninemia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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