PKM1 Recombinant Rabbit Monoclonal Antibody [PSH04-37] - BSA and Azide free

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Western blot analysis of PKM1 on different lysates with Rabbit anti-PKM1 antibody (HA722120) at 1/1,000 dilution.

Lane 1: HCT 116 cell lysate(20 µg/Lane)
Lane 2: U-87 MG cell lysate(20 µg/Lane)
Lane 3: HeLa cell lysate(20 µg/Lane)
Lane 4: human brain tissue lysate(40 µg/Lane)
Lane 5: mouse brain tissue lysate(40 µg/Lane)
Lane 6: mouse heart tissue lysate(40 µg/Lane)
Lane 7: mouse liver tissue lysate(40 µg/Lane)

Low expression: mouse liver

Exposure time: 14 seconds; ECL: K1801

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA722120, 1/1,000 in 5% NFDM/TBST, overnight at 4 ℃
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 58 kDa
Observed band size:58 kDa

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of HCT 116 cells labeling PKM1 with Rabbit anti-PKM1 antibody (HA722120) at 1/200 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-PKM1 antibody (HA722120) at 1/200 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) 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 (M1305-2, 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.

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human heart tissue with Rabbit anti-PKM1 antibody (HA722120) at 1/30,000 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 (HA722120) at 1/30,000 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.

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse heart tissue with Rabbit anti-PKM1 antibody (HA722120) at 1/5,000 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 (HA722120) at 1/5,000 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.

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat heart tissue with Rabbit anti-PKM1 antibody (HA722120) at 1/5,000 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 (HA722120) at 1/5,000 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.

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of HCT 116 cells labeling PKM1.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA722120, 1μg/mL) (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 (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

This data was developed using HA722120, the same antibody clone in a different buffer formulation.
Western blot analysis of PKM1 on different lysates with Rabbit anti-PKM1 antibody (HA722120) at 1/2,000 dilution.

Lane 1: Human PKM1 recombinant protein
Lane 2: Human PKM2 recombinant protein

Lysates/proteins at 50 ng/Lane.

Exposure time: 2 seconds; 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 (HA722120) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.