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BioReagent BioReagent for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
ATPase is widely distributed in the biological membrane enzyme systems of plants, animals, microorganisms, and cells. It functions as both a carrier and an enzyme, maintaining the cell membrane potential, regulating osmotic pressure, and providing the driving force for nutrient absorption. It plays an extremely important role in maintaining normal cellular physiological functions and can serve as a key evaluation indicator for cellular energy metabolism and functional integrity.
Detection Principle
Ca²⁺/Mg²⁺-ATPase decomposes ATP to generate ADP and inorganic phosphorus. Under acidic conditions, inorganic phosphorus reacts with ammonium molybdate to form ammonium phosphomolybdate, which is then reduced to form a blue phosphomolybdenum complex. This product has a characteristic absorption peak at 660 nm. The activity of Ca²⁺/Mg²⁺-ATPase can be characterized by the change in absorbance.
Applicable Samples: Serum (plasma), animal and plant tissues, cells, bacteria
| C1505940 | Component | 48T | 96T | Storage |
| C1505940A | Extraction Buffer | 60 mL | 60 mL×2 | 2-8℃ |
| C1505940B | Assay Buffer | 5 mL | 10 mL | 2-8℃ |
| C1505940C | Reagent Ⅰ | 1EA | 1EA | -20℃. Store in the dark. |
| C1505940D | Reagent Ⅱ | 1 mL | 2 mL | 2-8℃ |
| C1505940E | Reagent Ⅲ | 1EA | 1EA | 2-8℃. Store in the dark. |
| C1505940F | Reagent Ⅳ | 1EA | 1EA | 2-8℃. Store in the dark. |
| C1505940G | Reagent Ⅴ | 1EA | 1EA | 2-8℃. Store in the dark. |
| C1505940H | Reagent Ⅵ | 25 mL | 25 mL | 2-8℃ |
| C1505940I | Standard | 5 mL | 10 mL | 2-8℃ |
Note: Before formal testing, it is recommended to perform a preliminary experiment using 2-3 samples expected to have significant differences.
Required Instruments and Reagents
Microplate reader or visible spectrophotometer (capable of measuring absorbance at 660 nm)
Water bath
96-well plate or micro glass cuvettes, adjustable pipettes and tips
Deionized water
Homogenizer (for tissue samples)
Experimental Procedure
1. Reagent Preparation
| Reagent Name | Reagent Preparation | Notes |
| Extraction Buffer | Ready-to-use; Equilibrate to room temperature before use. | Store at 4℃ |
| Assay Buffer | Ready-to-use; Equilibrate to room temperature before use. | Store at 4℃ |
| Working Reagent Ⅰ | Dissolve in 7.2 mL deionized water immediately before use. | Unused reagent can be aliquoted and stored at -20℃ protected from light for 1 week; avoid repeated freeze-thaw cycles. |
| Reagent Ⅱ | Ready-to-use; Equilibrate to room temperature before use. | Store at 4℃ |
| Working Reagent Ⅲ | Dissolve in 3 mL deionized water immediately before use. | Unused reagent can be stored at 4℃ protected from light for up to 2 weeks. |
| Working Reagent Ⅳ | Dissolve in 25 mL deionized water immediately before use. | Unused reagent can be stored at 4℃ protected from light for up to 2 weeks. |
| Working Reagent Ⅴ | Dissolve in 25 mL deionized water immediately before use. | Unused reagent can be stored at 4℃ protected from light for up to 2 weeks. |
| Reagent Ⅵ | Ready-to-use; Equilibrate to room temperature before use. | Store at 4℃ |
| Standard | Ready-to-use; Equilibrate to room temperature before use. | Store at 4℃ |
| 0.5 μmol/mL Standard Phosphorus Application Solution | Dilute the Standard 20-fold: Take 0.1 mL Standard and add 1.9 mL deionized water, mix thoroughly. | |
| Phosphorus Assay Reagent | Prepare by mixing deionized water : Working Reagent Ⅳ : Working Reagent Ⅴ : Reagent Ⅵ = 2 : 1 : 1 : 1. The prepared reagent should be light yellow. | If colorless, the reagent has expired; if blue, indicates phosphorus contamination. Prepare the Phosphorus Assay Reagent freshly before use. |
Notes:
(1) Reagent Ⅲ has a pungent odor, Reagent Ⅴ is toxic, and Reagent Ⅵ is corrosive. It is recommended to perform the experiment in a fume hood.
(2) It is best to use new beakers, glass rods, and glass pipettes for reagent preparation, or use disposable plasticware to avoid phosphorus contamination.
2. Sample Preparation
Notes:
(1) Fresh samples are recommended. If not used immediately for experimentation, samples can be stored at -80°C for 1 month. Processed samples must be tested on the same day.
(2) If protein concentration measurement is required, the use of Aladdin's B665595 BCA Protein Quantification Kit or R1491648 Ready-to-Use BCA Protein Quantification Kit is recommended.
2.1 Plasma, Serum, and other liquid samples
Can be detected directly.
2.2 Animal tissue samples
Homogenize the tissue on ice with Extraction Buffer at a ratio of 0.1 g tissue to 1 mL Buffer. Centrifuge the homogenate at 4°C, 8,000 g for 10 min. Collect the supernatant and keep it on ice for testing.
2.3 Bacterial and cell samples
Collect 5 million cells or bacteria into a centrifuge tube. Wash the cells or bacteria with cold PBS, centrifuge, and discard the supernatant. Add 1 mL of Extraction Buffer. Disrupt the cells using ice-bath ultrasonication for 5 minutes (power 20% or 200 W, ultrasonic for 3 s, interval 7 s, repeat 30 times). Then centrifuge at 8,000 g, 4°C for 10 min. Collect the supernatant and keep it on ice for testing.
3.Experimental Steps
3.1 Preheat the microplate reader or visible spectrophotometer for at least 30 minutes. Set the wavelength to 660 nm. For the visible spectrophotometer, zero it with deionized water.
3.2 Enzymatic Reaction (Add the following reagents to EP tubes)
| Reagent (μL) | Control Tube | Test Tube |
| Assay Buffer | 65 | 45 |
| Working Reagent Ⅰ | 60 | 60 |
| Reagent Ⅱ | 0 | 20 |
| Sample | 0 | 100 |
Mix thoroughly and place in a water bath at 37°C (for mammals) or 25°C (for other species) for exactly 10 minutes.
| Working Reagent Ⅲ | 25 | 25 |
| Sample | 100 | 0 |
Mix thoroughly, centrifuge at 4,000 g, room temperature for 10 minutes, and collect the supernatant.
3.3 Phosphorus Assay (Add the following reagents to a 96-well plate or micro glass cuvettes)
| Reagent (μL) | Blank Well | Standard Well | Control Well | Test Well |
| 0.5 μmol/mL Standard P Application Solution | 0 | 20 | 0 | 0 |
| Supernatant | 0 | 0 | 20 | 20 |
| Deionized water | 20 | 0 | 0 | 0 |
| Phosphorus Assay Reagent | 200 | 200 | 200 | 200 |
3.4 Mix thoroughly and let stand at room temperature for 30 minutes. Measure the absorbance at 660 nm and record the values as ABlank, AStandard, AControl, and ATest.
Note: A control well is required for each sample. Only one blank well and one standard well are needed. It is recommended to perform a preliminary experiment with 2-3 samples expected to have large differences before the formal experiment. If (ATest - AControl) is less than 0.001, consider appropriately increasing the sample volume. If (ATest - AControl) is greater than 1.5, the sample can be further diluted with Extraction Buffer, and the calculated result should be multiplied by the dilution factor, or the amount of sample used for extraction can be reduced.
4. Calculation of Results
Note: We provide two types of calculation formulas: the derived process formula and the simplified formula. They are completely equivalent. It is recommended to use the simplified formula in bold as the final calculation formula.
4.1 Calculation of Ca²⁺/Mg²⁺-ATPase Activity in Serum (Plasma) and other liquid samples
Definition: One unit of enzyme activity is defined as the amount of enzyme that hydrolyzes ATP to produce 1 μmol of inorganic phosphorus per hour per milliliter of serum (plasma).
Ca²⁺/Mg²⁺-ATPase activity (U/mL) = CStandard × (ATest - AControl) ÷ (AStandard - ABlank) × VTotal ÷ VSample ÷ (T ÷ 60) = 7.5 × (ATest - AControl) ÷ (AStandard - ABlank)
4.2 Calculation of Ca²⁺/Mg²⁺-ATPase Activity in Tissues, Bacteria, or Cells
(1) Calculation based on protein concentration
Definition: One unit of enzyme activity is defined as the amount of enzyme that hydrolyzes ATP to produce 1 μmol of inorganic phosphorus per hour per milligram of tissue protein.
Ca²⁺/Mg²⁺-ATPase activity (U/mg) = CStandard × (ATest - AControl) ÷ (AStandard - ABlank) × VTotal ÷ (Cpr × VSample) ÷ (T ÷ 60) = 7.5 × (ATest - AControl) ÷ (AStandard - ABlank) ÷ Cpr
(2) Calculation based on sample fresh weight
Definition: One unit of enzyme activity is defined as the amount of enzyme that hydrolyzes ATP to produce 1 μmol of inorganic phosphorus per hour per gram of tissue.
Ca²⁺/Mg²⁺-ATPase activity (U/g) = CStandard × (ATest - AControl) ÷ (AStandard - ABlank) × VTotal ÷ (VSample ÷ VSample Total × W) ÷ (T ÷ 60) = 7.5 × (ATest - AControl) ÷ (AStandard - ABlank) ÷ W
(3) Calculation based on bacterial or cell density
Definition: One unit of enzyme activity is defined as the amount of enzyme that hydrolyzes ATP to produce 1 μmol of inorganic phosphorus per hour per 10⁴ bacteria or cells.
Ca²⁺/Mg²⁺-ATPase activity (U/10⁴) = CStandard × (ATest - AControl) ÷ (AStandard - ABlank) × VTotal ÷ (VSample ÷ VSample Total × 500) ÷ (T ÷ 60) = 0.015 × (ATest - AControl) ÷ (AStandard - ABlank)
Parameter Description:
CStandard: Concentration of the standard tube, 0.5 μmol/mL;
VTotal: Total volume of the enzymatic reaction, 0.25 mL;
VSample: Volume of sample added, 0.1 mL;
VSample Total: Volume of Extraction Buffer added, 1 mL;
T: Reaction time, 10 min;
Cpr: Sample protein concentration, mg/mL;
W: Sample fresh weight, g;
500: Total number of bacteria or cells, 5 million.
Precautions
1. Before formal testing, it is recommended to perform a preliminary experiment using 2-3 samples expected to have significant differences.
2. If protein concentration measurement is required, the use of Aladdin's B665595 BCA Protein Quantification Kit or R1491648 Ready-to-Use BCA Protein Quantification Kit is recommended.
3. Biochemical detection reagents are generally irritating, biologically toxic, etc. For your safety and health, please implement appropriate biosafety protection throughout the experiment, wear lab coats, masks, gloves, head covers, and other safety gear, and perform the experiment in a fume hood or biosafety cabinet.
4. This product is for scientific research use only. It is not intended for clinical diagnosis.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 10, 2026 | C1505940 | |
| Certificate of Analysis | Jun 02, 2026 | C1505940 | |
| Certificate of Analysis | May 26, 2026 | C1505940 | |
| Certificate of Analysis | Mar 27, 2026 | C1505940 | |
| Certificate of Analysis | Jan 08, 2026 | C1505940 |
| Sensitivity | Light-sensitive |
|---|
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