Methionine Adenosyltransferase I, alpha (MAT1A) Peptid
MAT1A
Reaktivität: Human
Wirt: Synthetic
BP, WB, IHC
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- Target Alle MAT1A Produkte
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-MAT1A antibody (Catalog #: ARP41398_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Aufreinigung
- Purified
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- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- Synonyme
- MAT Peptide, MATA1 Peptide, SAMS Peptide, SAMS1 Peptide, AdoMet Peptide, SADE Peptide, SAS Peptide, AI046368 Peptide, Ams Peptide, wu:fi35e01 Peptide, zgc:55442 Peptide, methionine adenosyltransferase 1A Peptide, methionine adenosyltransferase I, alpha Peptide, MAT1A Peptide, Mat1a Peptide, mat1a Peptide
- Hintergrund
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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.
Alias Symbols: MAT, MATA1, SAMS, SAMS1
Protein Size: 395 - Molekulargewicht
- 43 kDa
- Gen-ID
- 4143
- NCBI Accession
- NM_000429, NP_000420
- UniProt
- Q00266
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