GABA B Receptor 2 antibody [HL4937]

Whole zebrafish extract (30 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate.

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat tissues.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded human tissues.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat cerebellum.
Green: GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Red: beta Tubulin 3/ Tuj1 antibody [GT11710] (GTX631836) diluted at 1:500.
Blue: Fluoroshield with DAPI (GTX30920).
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse brain.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse olfactory bulb.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

GABA B Receptor 2 antibody [HL4937] detects GABA B Receptor 2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse hippocampus.
GABA B Receptor 2 stained by GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

Various tissue extracts (5 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data are based on NCBI database.

Non-transfected (–) and transfected (+) unboiled 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Boiled and unboiled various tissue extracts (50 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data are based on NCBI database.

Boiled and unboiled various tissue extracts (50 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GABA B Receptor 2 antibody [HL4937] (GTX645010) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.