beta 1 Adrenergic Receptor抗体 [HL3678]

Non-transfected (–) and transfected (+) unboiled MDA-MB-231 whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) detects beta 1 Adrenergic Receptor protein by flow cytometry analysis.
Sample: THP-1 and HeLa cells were blocked with an FcR blocking reagent for 10 minutes then fixed with 4% paraformaldehyde at 4 ºC for 15 minutes and washed with 0.1% saponin buffer.
The cells were following stained with beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) diluted at 1:50 or a Rabbit monoclonal IgG isotype control at 4ºC for 1 hour.
The classification of protein expression as positive or negative was primarily based on data from the Human Protein Atlas (HPA).

beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) detects beta 1 Adrenergic Receptor by flow cytometry analysis. Sample: Non-transfected and transfected 293T cells were fixed in 4% paraformaldehyde at 4ºC for 15 min and washed with 0.1% saponin buffer. The cells were following stained with beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) diluted at 1:50 or a Rabbit IgG isotype control (GTX35035) at 4ºC for 1 hour.

Whole cell extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Unboiled non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with beta 1 Adrenergic Receptor antibody [HL3678] (GTX641706) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.