Product Type: | Rabbit polyclonal IgG, primary antibodies |
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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*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size 61 kDa. |
Isotype: | IgG |
Immunogen: | Synthetic peptide within mouse GABRA4 aa 19-68 / 552. |
Positive control: | SH-SY5Y cell lysates, rat brain tissue, mouse brain tissue, SH-SY5Y. |
Subcellular location: | Postsynaptic cell membrane, cell membrane. |
Recommended Dilutions:
WB IHC-P |
1:500-1:2,000 1:50-1:200 |
Uniprot #: | SwissProt: P48169 Human | Q9D6F4 Mouse | P28471 Rat |
Alternative names: | GABA(A) receptor subunit alpha 4 GABA(A) receptor subunit alpha-4 GABR A4 GABRA 4 Gabra4 Gamma aminobutyric acid (GABA) A receptor alpha 4 Gamma aminobutyric acid A receptor alpha 4 Gamma aminobutyric acid receptor alpha 4 subunit Gamma aminobutyric acid receptor subunit alpha 4 Gamma-aminobutyric acid receptor subunit alpha-4 GBRA4_HUMAN |
Fig1: Western blot analysis of GABRA4 on SH-SY5Y cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ER1901-60, 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. | |
Fig2: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-GABRA4 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 (ER1901-60, 1/50) 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-GABRA4 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 (ER1901-60, 1/50) 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. |