ImmunofluorescenceA549 cells were fixed and permeabilized with 4% Paraformaldehyde and 0.5% Triton X-100. Fixed cells were stained with Mouse Anti-NIT2 Clone: NIT2-A48 (
Cat. No. SAB4100052) diluted to 1:5. The antibody was developed using Goat Anti-Mouse IgG, Cy3 conjugate. Cells were counterstained with DAPI (blue) to stain nuclei.
ImmunoblottingLysate of HEK-293T cells expressing FLAG
®-tagged human NIT2 was separated on SDS-PAGE, probed with Mouse Anti-NIT2 Clone: NIT2-A48 (
Cat. No. SAB4100052). The antibody was developed using Goat Anti-Mouse IgG-Peroxidase (
Cat. No. A2304) and a chemiluminescent substrate.
Lanes1. Antibody dilution 1:10,000
2. Negative control
3. Positive control Anti-FLAG
®
ImmunoblottingA549 cell extract was separated on SDS-PAGE and probed with Mouse Anti-NIT2 Clone: NIT2-A48 (
Cat. No. SAB4100048). The antibody was developed using Goat Anti-Mouse IgG-Peroxidase (
Cat. No. A2304) and a chemiluminescent substrate.
Lanes1. Antibody dilution 1:50
2. Antibody dilution 1:100
3. Negative control
Flow Cytometry1×10
6 A549 cells were fixed and permeabilized with 2% Paraformaldehyde and 0.1% Triton X-100. Fixed cells were labeled with Mouse Anti-NIT2 Clone: NIT2-A48 (
Cat. No. SAB4100052) diluted to 1:10 followed by Rabbit Anti-Mouse IgG, FITC conjugate. Shaded histogram: negative control without first antibody, Gray histogram: antibody specific staining.