LabAssay (TM) AST (GOT)
- for Cellbiology
- Manufacturer :
- FUJIFILM Wako Pure Chemical Corporation
- Storage Condition :
- Keep at 2-10 degrees C.
- GHS :
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100Tests
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In stock in Japan |
※Check availability in the US with the distributor.
Document
Kit component
For 100 tests
| Substrate-Enzyme Solution | 12 mL / 1 bottle |
|---|---|
| α-KG Solution | 11 mL / 1 bottle |
| AST Standard | 2 bottles |
| Buffer | 6 mL / 1 bottle |
| Stop Solution | 12 mL / 1 bottle |
Product Overview
Aspartate aminotransferase (AST) is an aminotransferase enzyme that catalyzes the conversion of L-aspartate and α-ketoglutarate into glutamate and oxaloacetate. AST is highly abundant in the liver, myocardium, and skeletal muscle and is released into the bloodstream due to increased cell permeability or cell death. Therefore, it serves as a marker for organ damage, including liver injury. AST is also useful indicators of liver fibrosis caused by conditions such as metabolic dysfunction-associated steatotic liver disease (MASLD).
LabAssay™ AST (GOT) is a kit used for the determination of AST in blood (serum, plasma). With the use of a microplate, this kit provides a quick and convenient method for measuring AST in samples.
[Note] LabAssay™ series are reagents for research purposes. It cannot be used for diagnostic purposes.
Kit Performance
| Analysis sample | Mouse Serum/Plasma Rat Serum/Plasma Dog Serum/Plasma Cat Serum/Plasma |
|---|---|
| Calibration curve range | 0-405 U/L |
| Sample volume | 7 μL |
| Measurement duration | Approx. 40 min |
| Wavelength | Primary wavelength 340 nm Reference wavelength 405 nm |
Example of Calibration Curve
Assay Principle
When a sample is mixed with Substrate-Enzyme Solution and α-KG Solution, glutamate and oxaloacetate are formed from L-aspartate and α-ketoglutarate in a reaction catalyzed by AST in the sample. The oxaloacetate thus produced is converted to malate by malate dehydrogenase (MDH). At the same time, NADH is oxidized to NAD, and the absorbance at 340 nm decreases. Finally, the reaction is stopped using a reaction Stop Solution, and the absorbance is measured to determine the AST activity value in the sample.
Data
Dilution Linearity Test
Serum and plasma (EDTA) from mouse, rat, dog and cat were serially diluted twofold with saline and measured in duplicate to assess linearity.
[Result]
All measurement results showed good linearity within the measurement range.
Spike and Recovery Test
Standard solutions at three concentrations were added to serum/plasma (EDTA) from mouse, rat, dog and cat. Next, spike recovery tests were conducted, with each measurement performed in duplicate.
Mouse sample (BALB/c)
| Spiked amount (U/L) |
Measurement value (U/L) |
Recovery volume (U/L) |
Recovery rate (%) |
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|---|---|---|---|---|
| Serum | - | ＜2.31 | - | - |
| 67.1 | 63.7 | 63.7 | 94.9 | |
| 98.7 | 90.0 | 90.0 | 91.2 | |
| 129 | 124 | 124 | 96.1 | |
| Average | 94.1 | |||
| Plasma (EDTA) |
- | ＜2.31 | - | - |
| 67.1 | 58.6 | 58.6 | 87.3 | |
| 98.7 | 93.7 | 93.7 | 94.9 | |
| 129 | 142 | 142 | 110 | |
| Average | 97.4 | |||
Rat sample (S.D. rat)
| Spiked amount (U/L) |
Measurement value (U/L) |
Recovery volume (U/L) |
Recovery rate (%) |
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|---|---|---|---|---|
| Serum | - | 34.8 | - | - |
| 16.1 | 52.6 | 17.8 | 111 | |
| 31.8 | 64.2 | 29.4 | 92.5 | |
| 91.8 | 135 | 100 | 109 | |
| Average | 104 | |||
| Plasma (EDTA) |
- | 32.4 | - | - |
| 15.5 | 47.4 | 15.0 | 96.8 | |
| 30.7 | 61.7 | 29.3 | 95.4 | |
| 88.8 | 128 | 95.6 | 108 | |
| Average | 100 | |||
Dog sample (Beagle)
| Spiked amount (U/L) |
Measurement value (U/L) |
Recovery volume (U/L) |
Recovery rate (%) |
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|---|---|---|---|---|
| Serum | - | 24.0 | - | - |
| 14.2 | 38.4 | 14.4 | 101 | |
| 28.2 | 56.7 | 32.7 | 116 | |
| 68.5 | 96.3 | 72.3 | 106 | |
| Average | 108 | |||
| Plasma (EDTA) |
- | 44.4 | - | - |
| 17.0 | 60.2 | 15.8 | 92.9 | |
| 33.7 | 77.2 | 32.8 | 97.3 | |
| 81.8 | 138 | 93.6 | 114 | |
| Average | 101 | |||
Cat sample (Japanese Cat)
| Spiked amount (U/L) |
Measurement value (U/L) |
Recovery volume (U/L) |
Recovery rate (%) |
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|---|---|---|---|---|
| Serum | - | 24.3 | - | - |
| 14.3 | 38.4 | 14.1 | 98.6 | |
| 28.3 | 51.3 | 27.0 | 95.4 | |
| 68.8 | 86.7 | 62.4 | 90.7 | |
| Average | 94.9 | |||
| Plasma (EDTA) |
- | 38.0 | - | - |
| 17.3 | 52.1 | 14.1 | 81.5 | |
| 34.2 | 69.4 | 31.4 | 91.8 | |
| 67.1 | 103 | 65.0 | 96.9 | |
| Average | 90.1 | |||
[Result]
Good recovery rates were confirmed.
FAQ
About sample
- Which anticoagulants can I use?
- Anticoagulants such as heparin, citrate and EDTA do not significantly influence the assay when used in normal amounts.
- What should I do with samples that exceed the measurable range?
- Dilute specimen with saline and repeat the assay if the measured value exceeds the measurable range, and multiply the result by the dilution factor.
- Is there any influence from substances that interfere with measurement (hemolysis, chyle, ascorbic acid, bilirubin, etc.)?
- Please treat the measured values of hemolyzed samples as reference values. Chyle, ascorbic acid, and bilirubin have almost no effect on the measured values. We have confirmed that there is no influence at the following concentrations.
Effects of interfering substances
Hemolysis No influence up to 25 mg/dL Chyle No influence up to 500 FTU Ascorbic acid No influence up to 50 mg/dL Bilirubin-F No influence up to 50 mg/dL Bilirubin-C No influence up to 10 mg/dL
About kit usage
- What instruments, and equipment are required for the assay using this kit?
- The instruments and equipment required for the use of this kit are listed below.
- 96-well microplate (transparent type)
- Micropipette
- Pipette
- Microtube
- Incubator maintained at 37 ℃
- Plate mixer
- Microplate reader with 340 nm/405 nm wavelength filter
- What is the amount of purified water to be added to the standard product?
- Find and check “Reconstitution of standard” on this product page. As the amount of purified water to be added varies by lot, be sure to check it for every lot.
Overview / Applications
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Manufacturer Information
Alias
For research use or further manufacturing use only. Not for use in diagnostic procedures.
Product content may differ from the actual image due to minor specification changes etc.
If the revision of product standards and packaging standards has been made, there is a case where the actual product specifications and images are different.