WB
Western blot analysis of CRKRS/CDK12 using anti-CRKRS/CDK12 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human K562 whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CRKRS/CDK12 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate. A specific band was detected for CRKRS/CDK12 at approximately 205 kDa. The expected band size for CRKRS/CDK12 is at 164 kDa.
IHC
IHC analysis of CRKRS/CDK12 using anti-CRKRS/CDK12 antibody.
CRKRS/CDK12 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. The tissue section was incubated with rabbit anti-CRKRS/CDK12 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of CRKRS/CDK12 using anti-CRKRS/CDK12 antibody.
CRKRS/CDK12 was detected in a paraffin-embedded section of human spleen tissue. The tissue section was incubated with rabbit anti-CRKRS/CDK12 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
ICC/IF analysis of CRKRS/CDK12 using anti-CRKRS/CDK12 antibody and anti-Beta Tubulin antibody.
CRKRS/CDK12 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-CRKRS/CDK12 Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody (green) and Fluoro550-conjugated Anti- mouse IgG Secondary Antibody (red) were used as secondary antibody.
IP
IP analysis of CRKRS/CDK12 using anti-CRKRS/CDK12 antibody in HepG2 whole cell lysate.
Western blot analysis of CRKRS/CDK12 using anti- CRKRS/CDK12 antibody.
Lane 1: HepG2 whole cell lysates(30ug),
Lane 2: Rabbit control IgG instead of anti- CRKRS/CDK12 antibody in HepG2 whole cell lysate,
Lane 3: anti- CRKRS/CDK12 antibody (2μg) + HepG2 whole cell lysate (500μg).
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti- CRKRS/CDK12 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate. A specific band was detected for CRKRS/CDK12 at approximately 200 kDa. The expected band size for CRKRS/CDK12 is at 164 kDa.
FC
Flow Cytometry analysis of HepG2 cells using anti-CRKRS/CDK12 antibody.
Overlay histogram showing HepG2 cells stained with A03495-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CRKRS/CDK12 Antibody at 1:100 dilution for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.