MAT1A Rabbit Polyclonal Antibody
cat.: HA500232
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: 44 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human MAT1A aa 370-395.
Positive control: Mouse liver tissue lysate, rat liver tissue lysate, human liver tissue lysate, rat liver tissue, mouse liver tissue.
Subcellular location: Cytosol.
Recommended Dilutions:
  WB
  IHC-P

1:2,000-1:5,000
1:400-1:1,000
Uniprot #: SwissProt: Q00266 Human | Q91X83 Mouse | P13444 Rat
Alternative names: AdoMet AdoMet synthetase 1 AI046368 Ams MAT MAT I/III MATA1 Methionine adenosyltransferase 1 Methionine adenosyltransferase I, alpha Methionine adenosyltransferase I/III MGC108563 S adenosylmethionine synthetase isoform type 1 SADE SAMS SAMS1
Images
HA500232_1.jpg Fig1: Western blot analysis of MAT1A on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA500232, 1/5,000) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: Mouse liver tissue lysate
Lane 2: Rat liver tissue lysate
Lane 3: Human liver tissue lysate
HA500232_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat liver tissue using anti-MAT1A antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500232, 1/400) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA500232_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-MAT1A antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500232, 1/400) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.