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Aspartate Aminotransferase (AST/GOT) Activity Assay Kit– MSE Supplies LLC

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Aspartate Aminotransferase (AST/GOT) Activity Assay Kit

SKU: E-BC-K236-M-500

  • $ 40895



Aspartate Aminotransferase (AST/GOT) Activity Assay Kit

SKU # E-BC-K236-M
Detection Instrument Microplate reader (500-520 nm)
Detection method Colorimetric method


Product Details

Properties

Synonyms AST, GOT, Glutamic-oxalacetic transaminase
Sample Type Serum, plasma, animal tissue, cells, cell culture supernatant
Sensitivity 1.1 IU/L
Detection Range 1.1-72.3 IU/L
Detection Method Colorimetric method
Assay type Enzyme Activity
Assay time 80 min
Precision Average inter-assay CV: 6.800% | Average intra-assay CV: 5.300%
Other instruments required Micropipettor, Vortex mixer, Incubator, Multichannel pipette
Other reagents required Normal saline (0.9% NaCl), PBS (0.01 M, pH 7.4)
Storage 2-8℃
Valid period 12 months


Images

H Xia et al investigate the relationship between insulin resistance and GSK3β-FBXW7-ERRα transcriptional axis. Aspartate aminotransferase (AST) activity in mouse serum was determined using AST activity assay kit (E-BC-K236-M).

No significant difference of AST activity was observed between WT and 3SA mice after HFD for 17 weeks.

 

Dilution of Sample

It is recommended to take 2~3 samples with expected large difference to do pre-experiment before formal experiment and dilute the sample according to the result of the formal experiment and the detection range (1.1-72.3 IU/L).

The recommended dilution factor for different samples is as follows (for reference only):

Sample type Dilution factor
Human serum 1
Human plasma 1
Porcine serum 1
Rat serum 1
HC-60 cellular supernatant 1
Calu-3 cellular supernatant 1
10% Rat liver tissue homogenization 15-30
10% Rat lung tissue homogenization 2-8

 

Note: The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4).

 

Detection Principle

AST/GOT enables alpha-ketoglutaric acid and aspartic acid to displace amino and keto groups to form glutamic acid and oxaloacetic acid. Oxaloacetic acid can decarboxylate itself to form Pyroracemic acid during the reaction. Pyroracemic acid reacted with 2,4-dinitrophenylhydrazine(DNPH) to form 2,4, dinitrophenylhydrazone showing reddish brown in alkaline solution. Measure the OD values and calculate the enzyme activity.

 

Kit Components & Storage

Item Component Size 1(48 T) Size 2(96 T) Storage
Reagent 1 Buffer Solution 0.5 mL × 1 vial 0.5 mL × 1 vial 2-8℃, 12 months
Reagent 2 2 mmol/L Sodium
Pyruvate
0.5 mL × 1 vial 0.5 mL × 1 vial 2-8℃, 12 months
Reagent 3 Substrate Solution 2.5 mL × 1 vial 5 mL × 1 vial 2-8℃, 12 months
Reagent 4 Chromogenic Agent 2.5 mL × 1 vial 5 mL × 1 vial 2-8°C, 12 months, shading light
Reagent 5 Alkali Reagent 2.5 mL × 1 vial 5 mL × 1 vial 2-8℃, 12 months
Microplate 96 wells No requirement
Plate Sealer 2 pieces

 

Note: The reagents must be stored strictly according to the preservation conditions in the above table. The reagents in different kits cannot be mixed with each other. For a small volume of reagents, please centrifuge before use, so as not to obtain sufficient amount of reagents.

 

Technical Data:

Parameter:

Intra-assay Precision

Three human serum samples were assayed in replicates of 20 to determine precision within an assay. (CV = Coefficient of Variation)

Parameters Sample 1 Sample 2 Sample 3
Mean (Carmen unit) 24.00 61.00 114.00
%CV 7.9 6.4 6.1


Inter-assay Precision

Three human serum samples were assayed 17 times in duplicate by three operators to determine precision between assays.

Parameters Sample 1 Sample 2 Sample 3
Mean (Carmen unit) 24.00 61.00 114.00
%CV 5.5 5.0 5.4


Recovery

Take three samples of high concentration, middle concentration and low concentration to test the samples of each concentration for 6 times parallelly to get the average recovery rate of 97%.

Parameters Standard 1 Standard 2 Standard 3
Expected Conc.
(Carmen unit)
24 61 114
Observed Conc.
(Carmen unit)
26.04 59.85 153
Recovery rate (%) 96 97 99

 

Sensitivity

The analytical sensitivity of the assay is 1.1 IU/L. This was determined by adding two standard deviations to the mean O.D. obtained when the zero standard was assayed 20 times, and calculating the corresponding concentration.

 

Standard Curve

As the OD value of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique or temperature effects), so the standard curve and data are provided as below for reference only:

Carmen Unit 0 24 61 114 190
Average OD 0.222 0.293 0.361 0.423 0.479
Absoluted OD 0 0.071 0.139 0.201 0.257