ImmunofluorescenceHeLa cells were fixed and permeabilized with 4% paraformaldehyde followed by 0.5% Triton
™ X-100. Fixed cells were stained with 2 μg/mL Rabbit Anti-EXOSC5 (N-Terminal) (
Cat. No. SAB4200439). The antibody was developed using Goat Anti-Rabbit IgG, Cy3
™ conjugate. Cells were counterstained with DAPI (blue) to stain nuclei.
ImmunoblottingWhole extract of HEK-293T cells was separated on SDS-PAGE and probed with Rabbit Anti-EXOSC5 (N-terminal) (
Cat. No. SAB4200439). The antibody was developed using Goat Anti-Rabbit IgG-Peroxidase (
Cat. No. A0545) and a chemiluminescent substrate.
Lanes1. 2 μg/mL antibody
2. 1 μg/mL antibody
3. 2 μg/mL antibody + EXOSC5 immunizing peptide
ImmunoprecipitationRabbit Anti-EXOSC5 (N-Terminal) (
Cat. No. SAB4200439) was used to immunoprecipitate EXOSC5 from HeLa whole cell extract.
Detection antibody: Rabbit Anti-EXOSC5 (C-Terminal) (
Cat. No. SAB4200438).
Lanes1. 10 μg antibody
2. 5 μg antibody
3. 2.5 μg antibody
4. Negative control: non-relevant antibody
5. Negative control: without 1st antibody
6. Negative control: without cell extract