Methionine Adenosyltransferase I, alpha (MAT1A) Peptide
MAT1A
Reactivité: Humain
Hôte: Synthetic
BP, WB, IHC
-
- Antigène Tous les produits MAT1A
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- Origine
- Humain
-
Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Attributs du produit
- 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.
- Purification
- Purified
-
-
- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
-
- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
-
- Antigène
- MAT1A (Methionine Adenosyltransferase I, alpha (MAT1A))
- Synonymes
- 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
- Sujet
-
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 - Poids moléculaire
- 43 kDa
- ID gène
- 4143
- NCBI Accession
- NM_000429, NP_000420
- UniProt
- Q00266
-
Vous êtes ici:
