Catalase (CAT) Activity Assay Kit, 100 Assays (50 Samples), 50 Assays (25 Samples)
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Catalase (CAT) Activity Assay Kit, 100 Assays (50 Samples), 50 Assays (25 Samples)

Cat.No: CMAK-YJL-0115 Datasheet

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Product Details Background Product Features Product Advantages Related Products
Product Name Catalase (CAT) Activity Assay Kit, 100 Assays (50 Samples), 50 Assays (25 Samples)
Catalog No. CMAK-YJL-0115
Size 100 Assays (50 samples), 50 Assays (25 samples)
Sample Type Serum (plasma); cells; animal and plant tissues
Detection Instrument UV-Visible spectrophotometer (405 nm)
Research Field Oxidative stress
Sensitivity 0.27 U/mL
Detection Range 0.27-155.4 U/mL
Accuracy Inter-assay variation: 5.1% | Intra-assay variation: 3.1%
Sample Size 0.1-0.2 mL
Storage The product can be stored at 2-8°C, protected from light for 6 months.
Shelf Life 6 months
Index Abbreviation CAT
Detection Time 1 h 10 min
Intended Use For research use only.

Catalase (EC 1.11.1.6), a critical antioxidant enzyme ubiquitous in nearly all aerobic organisms—from mammalian cells to plant tissues and microorganisms—plays an irreplaceable role in safeguarding cells against oxidative damage. Its core biological function is to catalyze the rapid decomposition of hydrogen peroxide (H₂O₂), a toxic byproduct of cellular metabolism (e.g., mitochondrial respiration and peroxisomal reactions), into non-harmful water (H₂O) and oxygen (O₂) through the reaction: 2H₂O₂ → 2H₂O + O₂. This reaction occurs at an extremely high catalytic rate—near the diffusion-controlled limit—making catalase one of the most efficient enzymes known, capable of breaking down millions of H₂O₂ molecules per second per enzyme molecule.

Why Catalase Activity Measurement Matters?

Oxidative Stress Research: Oxidative stress, caused by an imbalance between the production of reactive oxygen species (ROS) (including H₂O₂) and the body’s antioxidant defense system, is closely linked to the pathogenesis of numerous diseases. For example, elevated H₂O₂ levels due to reduced catalase activity have been associated with neurodegenerative disorders (Alzheimer’s disease, Parkinson’s disease), cardiovascular diseases (atherosclerosis, hypertension), diabetes, and even aging processes. Measuring catalase activity helps researchers assess the severity of oxidative stress in biological samples and explore the mechanisms of disease progression.
Cellular Protection Mechanisms: In eukaryotic cells, catalase is primarily localized in peroxisomes, where it works in synergy with other antioxidant enzymes (e.g., superoxide dismutase, glutathione peroxidase) to maintain redox homeostasis. For instance, in liver and kidney cells—organs with high metabolic activity—catalase accounts for over 60% of H₂O₂ decomposition, preventing lipid peroxidation, protein oxidation, and DNA damage that would otherwise lead to cell death or dysfunction.
Diverse Research Applications: Catalase activity analysis is not limited to medical and physiological research. It is also widely used in agricultural science (e.g., evaluating the stress tolerance of crops to drought, salinity, or heavy metal exposure), environmental science (e.g., monitoring the impact of pollutants on aquatic organisms’ antioxidant systems), and food science (e.g., assessing the freshness and shelf life of food products by detecting catalase activity in raw materials).

Challenges in Traditional Catalase Activity Assays

Traditional methods for measuring catalase activity, such as direct UV spectrophotometry (monitoring H₂O₂ absorption at 240 nm), often face significant limitations:
Sample Interference: Biological samples (e.g., serum, tissue homogenates) contain proteins, nucleic acids, and other substances that absorb at 240 nm, leading to inaccurate results.
Low Sensitivity: These methods struggle to detect low catalase activity levels (e.g., in dilute cell lysates or early-stage disease samples), limiting their applicability in subtle oxidative stress studies.
Complex Operation: Many traditional assays require strict control of reaction temperature and time, with cumbersome reagent preparation steps that increase experimental variability and labor costs.

Our Catalase (CAT) Activity Assay Kit addresses these challenges by adopting an optimized colorimetric/UV-visible detection method, ensuring high sensitivity, specificity, and ease of use for reliable catalase activity quantification across diverse sample types.

Broad Sample Compatibility: The kit is designed to work with multiple common sample types, including serum, plasma, cultured cells (both adherent and suspension cells), and animal/plant tissues (e.g., liver, kidney, leaf, root tissues). This eliminates the need for researchers to purchase separate kits for different sample sources, reducing experimental costs and simplifying workflow.
High Sensitivity and Wide Detection Range: With a sensitivity of 0.27 U/mL and a detection range of 0.27–155.4 U/mL, the kit can accurately measure both low and high catalase activity levels. This makes it suitable for samples with varying activity concentrations, from dilute cell supernatants to high-activity liver tissue homogenates.
Excellent Assay Precision: The kit exhibits low inter-assay variation (5.1%) and intra-assay variation (3.1%), ensuring consistent and reproducible results across different experiments, operators, or time points. This reliability is critical for publishing high-quality research data and validating experimental conclusions.
Time-Efficient Operation: The total detection time is only 1 hour and 10 minutes, significantly shorter than traditional assays (which often take 2 or more hours). This reduces experimental turnaround time, allowing researchers to process more samples or complete multiple experiments in a single day.
Stable and Easy Storage: All kit components can be stored at 2–8°C (protected from light) for up to 6 months, eliminating the need for expensive -20°C or -80°C storage equipment. The reagents remain stable during transportation (when shipped with appropriate cold packs), ensuring no loss of activity upon arrival.
User-Friendly Protocol: The kit includes pre-formulated reagents (no complex dilution or preparation required) and a detailed, step-by-step instruction manual. Even researchers with limited experience in enzyme assays can complete the experiment smoothly, minimizing operational errors.

Superior Specificity to Avoid Interference: Unlike traditional UV-based assays, our kit uses a reaction system that specifically targets catalase-catalyzed H₂O₂ decomposition, with reagents that do not react with other components in biological samples (e.g., proteins, lipids, or other antioxidant enzymes). This avoids false positive/negative results caused by sample matrix interference, ensuring accurate quantification of catalase activity.
Minimal Sample Requirement: Only 0.1–0.2 mL of sample is needed per assay, which is particularly beneficial for precious or hard-to-obtain samples (e.g., rare clinical serum samples, limited primary cell cultures, or small plant tissues). This reduces sample waste and allows researchers to maximize the use of valuable biological materials.
Cost-Effective Assay Design: The kit is available in two sizes—100 assays (for 50 samples) and 50 assays (for 25 samples)—allowing researchers to choose the appropriate size based on their experimental needs. This flexible sizing prevents over-purchasing and reduces unnecessary costs, especially for small-scale experiments or preliminary studies.
Compatible with Standard Laboratory Equipment: The kit uses a UV-visible spectrophotometer (detection at 405 nm), a common instrument in most research laboratories. There is no need to invest in specialized equipment (e.g., fluorescence microplate readers or HPLC systems), lowering the barrier to entry for researchers with limited laboratory resources.
Research-Validated Performance: The kit’s performance (sensitivity, precision, detection range) has been validated through extensive testing with standard catalase samples and real biological specimens (e.g., human serum, mouse liver homogenates, HeLa cell lysates). This validation ensures that the results obtained are consistent with industry standards and suitable for inclusion in scientific publications.

For research use only, not for clinical use.

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