ImmunofluorescenceA431 cells were fixed and permeabilized with 4% paraformaldehyde followed by 0.5% Triton
™ X-100. Fixed cells were stained with 5 μg/mL Rabbit Anti-Rab13 (C-terminal) (
Cat. No. SAB4200058). The antibody was developed using Goat Anti-Rabbit IgG, Atto 488 conjugate (
Cat. No. 18772).Cells were counterstained with DAPI (blue) to stain nuclei (×100 magnification).
ImmunofluorescenceNIH-3T3 cells were fixed and permeabilized with 4% paraformaldehyde followed by 0.5% Triton
™ X-100. Fixed cells were stained with 5 μg/mL Rabbit Anti-Rab13 (C-terminal) (
Cat. No. SAB4200058). The antibody was developed using Goat Anti-Rabbit IgG, Atto 488 conjugate (
Cat. No. 18772).Cells were counterstained with DAPI (blue) to stain nuclei (×100 magnification).
ImmunoblottingWhole extract of NT2 cells was separated on SDS-PAGE and probed with Rabbit Anti-Rab13 (C-terminal) (
Cat. No. SAB4200058). The antibody was developed using Goat Anti-Rabbit IgG-Peroxidase (
Cat. No. A0545) and a chemiluminescent substrate.
Lanes1. 2 μg/mL antibody
2. 5 μg/mL antibody
3. 5 μg/mL antibody + Rab13 immunizing peptide (human, 183-198)
ImmunoprecipitationRabbit Anti-Rab13 (C-terminal) (
Cat. No. SAB4200058), was used to immunoprecipitate Rab13 from NT2 whole cell extract. Detection antibody: Rabbit Anti-Rab13.
Lanes1. 5 μg antibody
2. 10 μg antibody
3. Negative control: 10 μg non-relevant antibody
4. Positive control: NT2 whole cell extract