NMDAR2A Recombinant Rabbit Monoclonal Antibody [JA31-20]
cat.: ET1704-80
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, IF-Tissue
Clonality: Monoclonal
Clone number: JA31-20
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: 165 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human NMDAR2A aa 1356-1405 / 1464.
Positive control: Rat brain tissue lysate, rat brain tissue, rat skin tissue, human brain tissue, mouse small intestine tissue.
Subcellular location: Cell membrane, postsynaptic cell membrane, dendritic spine, synapse, Cytoplasmic vesicle membrane.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue

1:500
1:50-1:100
1:200
Uniprot #: SwissProt: Q12879 Human | P35436 Mouse | Q00959 Rat
Alternative names: EPND FESD GluN2A Glutamate [NMDA] receptor subunit epsilon-1 Glutamate receptor Glutamate receptor ionotropic N methyl D aspartate 2A GRIN 2A GRIN2A hNR2A LKS N methyl D aspartate receptor channel, subunit epsilon 1 N Methyl D Aspartate Receptor Subtype 2A N methyl D aspartate receptor subunit 2A N-methyl D-aspartate receptor subtype 2A NMDA receptor subtype 2A NMDAR 2A NMDAR2A NMDE1_HUMAN NR2A OTTHUMP00000160135 OTTHUMP00000174531
Images
ET1704-80_1.jpg Fig1: Western blot analysis of NMDAR2A on mouse hippocampus tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1704-80, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
ET1704-80_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-NMDAR2A antibody (ET1704-80) at 1/50 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-80) at 1/50 dilution for 1 hour 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.
ET1704-80_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat skin tissue using anti-NMDAR2A antibody. Counter stained with hematoxylin.
ET1704-80_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human brain tissue using anti-NMDAR2A antibody. Counter stained with hematoxylin.
ET1704-80_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse small intestine tissue using anti-NMDAR2A antibody. Counter stained with hematoxylin.
ET1704-80_6.jpg Fig6: Immunofluorescence analysis of paraffin-embedded human brain tissue labeling NMDAR2A with Rabbit anti-NMDAR2A antibody (ET1704-80) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (ET1704-80, green) at 1/200 dilution overnight at 4 ℃, washed with PBS.

Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.