beta-2 Adrenergic R/ADRB2 Antibody (JM102-06)

Western Blot: beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] -

Western Blot: beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] -Analysis of beta 2 Adrenergic Receptor on different lysates with Rabbit anti-beta 2 Adrenergic Receptor antibody at 1/1,000 dilution.Lane 1: A431 cell lysate (no heat) (15 µg/Lane)Lane 2: Mouse kidney tissue lysate (no heat) (20 µg/Lane)Lane 3: Mouse heart tissue lysate (no heat) (20 µg/Lane)Lane 4: Rat kidney tissue lysate (no heat) (20 µg/Lane)Lane 5: Zebrafish tissue lysate (20 µg/Lane)Predicted band size: 46 kDaObserved band size: 55-100 kDaExposure time: 3 minutes; ECL: K1801;4-20% SDS-PAGE gel.Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1703-04) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.

Flow Cytometry-beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] -

Flow Cytometry-beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] -Analysis of A431 cells labeling beta 2 Adrenergic Receptor.Cells were fixed and permeabilized. Then stained with the primary antibody (1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

ICC/IF-beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] -

ICC/IF-beta-2 Adrenergic R/ADRB2 Antibody (JM102-06) [NBP2-67187] - Analysis of A431 cells labeling beta 2 Adrenergic Receptor with Rabbit anti-beta 2 Adrenergic Receptor antibody at 1/100 dilution.Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-beta 2 Adrenergic Receptor antibody at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.Beta tubulin ( red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.