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Products:Tags & Cell Markers >> Subcellular Markers >> Organelles >> Peroxisome
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Read our guarantee »Anti-Catalase antibody - Peroxisome Marker
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Rabbit polyclonal to Catalase - Peroxisome Marker
ICC/IF, WBmore details
Reacts with
Mouse, Rat, Chicken, Human
Catalase (Bovine Liver)
This antibody gave a positive control in the following Tissue Lysates: Human Liver, Mouse Liver, Rat Liver, Chicken Liver
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS, pH 7.4
Concentration information loading...
Protein A purified
Polyclonal
IgG
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Redox metabolism >> Antioxidants
Cancer >> Cancer Metabolism >> Cellular metabolic process
Cardiovascular >> Heart >> Cardiac metabolism
Signal Transduction >> Protein Trafficking >> Chaperones >> Heat Shock Proteins
Tags & Cell Markers >> Subcellular Markers >> Organelles >> Peroxisome
Our Abpromise guarantee covers the use of ab15834 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use a concentration of 5 µg/ml.
WB: Use a concentration of 5 µg/ml. Detects a band of approximately 65 kDa (predicted molecular weight: 60 kDa).
Occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells.
Defects in CAT are the cause of acatalasia (ACATLAS) [MIM:115500]; also known as acatalasemia. This disease is characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions.
Belongs to the catalase family.
The N-terminus is blocked.
Peroxisome.
Target information above from: UniProt accessionP04040
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Catalase antibody (ab15834)

All lanes : Anti-Catalase antibody - Peroxisome Marker (ab15834) at 5 µg/ml
Lane 1 : Catalase at 0.1 µg
Lane 2 : Human Liver lysate at 20 µg
Lane 3 : Mouse Liver lysate at 20 µg
Lane 4 : Rat Liver lysate at 20 µg
Lane 5 : Chicken Liver lysate at 20 µg
Secondary
Alexa Fluor Goat polyclonal to Rabbit IgG (700) at 1/10000 dilution
Predicted band size : 60 kDa
Observed band size : 65 kDa (why is the actual band size different from the predicted?)
Western blot

All lanes : Anti-Catalase antibody - Peroxisome Marker (ab15834) at 5 µg/ml
Lane 1 :
Lane 2 :
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Exposure time : 10 seconds
Immunocytochemistry/ Immunofluorescence - Catalase antibody - Peroxisome Marker (ab15834)

ICC/IF image of ab15834 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab15834, 5µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 phalloidin was used to label F-actin (red).
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab15834? Please let us know so that we can cite the reference in this datasheet
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ICC/IF image of ab15834 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab15834, 5µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 phalloidin was used to label F-actin (red).
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