MAT1A Antikörper
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- Target Alle MAT1A Antikörper anzeigen
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
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Reaktivität
- Human, Maus, Ratte, Hund, Drosophila melanogaster, C. elegans
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser MAT1A Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Aufreinigung
- Antibody is purified by protein A chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MAT1A.
- Top Product
- Discover our top product MAT1A Primärantikörper
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- Applikationshinweise
- MAT1A antibody can be used for detection of MAT1A by ELISA at 1:1562500. MAT1A antibody can be used for detection of MAT1A by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Konzentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handhabung
- As with any antibody avoid repeat freeze-thaw cycles.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store MAT1A antibody at -20 °C.
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- Target
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- Andere Bezeichnung
- MAT1A (MAT1A Produkte)
- Synonyme
- MAT antikoerper, MATA1 antikoerper, SAMS antikoerper, SAMS1 antikoerper, AdoMet antikoerper, SADE antikoerper, SAS antikoerper, AI046368 antikoerper, Ams antikoerper, wu:fi35e01 antikoerper, zgc:55442 antikoerper, methionine adenosyltransferase 1A antikoerper, methionine adenosyltransferase I, alpha antikoerper, MAT1A antikoerper, Mat1a antikoerper, mat1a antikoerper
- Hintergrund
- 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.
- Molekulargewicht
- 43 kDa
- Gen-ID
- 4143
- NCBI Accession
- NP_000420
- UniProt
- Q00266
- Pathways
- Mitotic G1-G1/S Phases, M Phase, Ribonucleoside Biosynthetic Process, Methionine Biosynthetic Process
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