![All lanes : Anti-ACADS antibody [7E1AB5] (ab110318) at 1 µg/mlLane 1 : HepG2 whole cell cells at 10 µgLane 2 : ACADS at 0.01 µg](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_1/1502_ACADS-Primary-antibodies-ab110318-1.gif)
All lanes : Anti-ACADS antibody [7E1AB5] (ab110318) at 1 µg/mlLane 1 : HepG2 whole cell cells at 10 µgLane 2 : ACADS at 0.01 µg
Immunocytochemistry image of stained human fibroblasts. The cells were paraformaldehyde fixed (4%, 20 minutes) and Triton X-100 permeabilized (0.1%, 15 minutes). The cells were incubated with the ab110318 (1 µg/ml) for 2 hours at room temperature or over night at 4°C. The secondary antibody was (red) Alexa Fluor® 594 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. The target protein locates to the mitochondrial matrix.
IHC image of ACADS staining in Human heart formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab110318, 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.