Ab59457 staining human normal skin tissue. Staining is localised to mitochondria.Left panel: with primary antibody at 2 ug/ml. Right panel: isotype control.Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.

All lanes : Anti-Hsp60 antibody [LK-1] (ab59457) at 0.05 µg/mlLane 1 : Rat Brain tissue lysatesLane 2 : Rat Heart tissue lysatesLane 3 : Rat Kidney tissue lysatesLane 4 : Rat Liver tissue lysatesLane 5 : Rat Lung tissue lysatesLane 6 : Rat Pancreas tissue lysatesLane 7 : Rat skeletal muscle tissue lysateLane 8 : Rat Spleen tissue lysateLane 9 : Rat Testes tissue lysateLane 10 : Rat Thymus tisuue lysateLane 11 : Cell lysates prepared from rat heart H9C2 cellsLane 12 : Cell lysates prepared from mouse NIH3T3 cellsLane 13 : Cell lysates prepared from mouse Pam212 cellsLysates/proteins at 10 µg per lane.SecondaryHRP-conjugated goat polyclonal to mouse IgG1 at 1/10 dilution

Overlay histogram showing HeLa cells stained with ab59457 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab59457, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.

Hsp60 was immunoprecipitated using 0.5mg Rat Brain tissue lysate, 5µg of Mouse monoclonal to Hsp60 and 50µl of protein G magnetic beads (+). No antibody was added to the control (-). The antibody was incubated under agitation with Protein G beads for 10min, Rat Brain tissue lysate lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab59457.Secondary: Goat polyclonal to mouse IgG light chain specific (HRP) at 1/20,000 dilution.Band: 60kDa; Hsp60: non specific bands - 50kDa: We are unsure as to the identity of this extra band.