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Immunohistochemical staining of human Prostate shows strong nuclear positivity in glandular cells.
Immunohistochemical staining of human Prostate shows strong nuclear positivity in glandular cells.
Immunohistochemical staining of human Prostate shows strong nuclear positivity in glandular cells.

Anti-MAT2A Antibody

HPA043028
Atlas Antibodies
ApplicationsWestern Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
DownloadDatasheet
DownloadMSDS
Product group Antibodies
ReactivityHuman
TargetMAT2A
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-MAT2A
  • Delivery Days Customer
    4
  • Applications
    Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID4144
  • Target name
    MAT2A
  • Target description
    methionine adenosyltransferase 2A
  • Target synonyms
    adoMet synthase 2; adoMet synthetase 2; MAT 2; MATA2; MATII; MAT-II; methionine adenosyltransferase 2; methionine adenosyltransferase II, alpha; S-adenosylmethionine synthase isoform type-2; SAMS2; testicular tissue protein Li 121
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP31153
  • Protein Name
    S-adenosylmethionine synthase isoform type-2
  • Scientific Description
    Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
  • Reactivity
    Human
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116161

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Figure 1. Western blot analysis of MAT2A using anti-MAT2A antibody (A04557-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U-937 whole cell lysates, Lane 4: human Daudi whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAT2A antigen affinity purified polyclonal antibody (Catalog # A04557-1) at 0.25 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAT2A at approximately 50 kDa. The expected band size for MAT2A is at 44 kDa.
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