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A-CoA(Acetyl Coenzyme A) ELISA Kit - 1
  • A-CoA(Acetyl Coenzyme A) ELISA Kit - 1
  • A-CoA(Acetyl Coenzyme A) ELISA Kit - 2
  • A-CoA(Acetyl Coenzyme A) ELISA Kit - 3
All Size Price Qty
96T $ 495.00
- +
48T $ 396.00
- +
24T $ 150.00
- +
96T*5 Inquire /
96T*10 Inquire /
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For research use only.

Product Summary
Sensitivity 0.19 ng/mL
Detection Range 0.31-20 ng/mL
Sample Volume 100 μL
Total Assay Time 3 h 30 min
Reactivity Universal
Specificity This kit recognizes Universal A-CoA in samples.No significant cross-reactivity or interference between Universal A-CoA and analogues was observed
Recovery 80%-120%
Sample Type Serum, plasma and other biological fluids
Detection Method Colorimetric method, ELISA, Sandwich
Assay Type Sandwich-ELISA
Size 96T / 48T / 24T / 96T*5 / 96T*10
Storage 2-8℃
Expiration Date 12 months
Typical data
The following data was generated by the Quality Control Department, under controlled laboratory conditions (ambient temperature: 18-25 °C, relative humidity: 35-75%) using standardized procedures (TMB reaction at 37 °C in the dark for 15 minutes, followed by termination and OD measurement). These values are provided for reference only. Actual results may vary due to differences in laboratory conditions, operator technique, and equipment. Users are required to generate a standard curve using their own experimental data.
ng/mL OD1 OD2 Mean OD Corrected OD
20 2.326 2.308 2.317 2.226
10 1.720 1.774 1.747 1.656
5 1.033 1.063 1.048 0.957
2.5 0.568 0.550 0.559 0.468
1.25 0.345 0.333 0.339 0.248
0.63 0.207 0.203 0.205 0.114
0.31 0.147 0.155 0.151 0.060
0 0.088 0.094 0.091 -
Precision
Intra-assay Precision (Within-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
/ Intra-assay Precision Inter-assay Precision
Sample 1 2 3 1 2 3
Numbers 20 20 20 20 20 20
Mean(ng/mL) 0.990 2.400 7.260 0.960 2.310 7.720
Standard deviation 0.060 0.140 0.500 0.070 0.200 0.620
CV(%) 5.730 5.890 6.840 7.500 8.710 8.000
Recovery
The recovery of Universal A-CoA was evaluated by spiking samples at low, mid, and high concentrations across the assay range in various sample matrices.
The assay performance was assessed by comparing the measured concentrations to the expected spiked amounts to determine the percent recovery.
Sample Type Range (%) Average Recovery(%)
Cell culture media (n=8) 93-108 99
Serum (n=8) 88-99 94
EDTA plasma (n=8) 86-97 91
Linearity
Linearity of the assay was evaluated by spiking samples with high concentrations of Universal A-CoA and performing serial dilutions using Standard & Sample Diluent to produce concentrations spanning the assay's dynamic range. The measured values were then compared to the expected concentrations to assess the linearity of response.
/ / Cell culture media
(n=5)
EDTA plasma
(n=5)
Serum
(n=5)
1:2 Range 92-109 93-110 90-102
Average 99 100 96
1:4 Range 84-97 82-98 90-102
Average 91 89 96
1:8 Range 87-101 82-93 93-106
Average 93 87 99
Stability
Each kit batch is subjected to accelerated stability testing and real-time stability monitoring. Sample performance is evaluated after storage at 37 °C for 10 days to assess the impact of elevated temperature on assay reliability and reagent integrity.
/ Variation range of 37°C mean
concentration / 2-8°C mean
Sample 1(n=16) 98.02-105.66
Sample 2(n=16) 90.58-107.58
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Universal A-CoA. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Universal A-CoA and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Universal A-CoA, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Universal A-CoA. You can calculate the concentration of Universal A-CoA in the samples by comparing the OD of the samples to the standard curve.
Acetyl-CoA is a component of cellular respiration that is mainly used to add acetyl groups in biochemical reactions. These reactions involve the metabolism of proteins, carbohydrates, and lipids, providing energy sources such as adenosine triphosphate (ATP), lactate, and ketones. Acetyl CoA, as a central metabolic intermediate, its abundance reflects the general energy state of cells, and its concentraion affects the activity or specificity of various enzymes, whether through conformational changes or changes in substrate availability. Acetyl CoA is the sole donor of protein acetylation and a key substrate in the tricarboxylic acid cycle, which is crucial for the biosynthesis of fatty acids and isoprene. In addition, acetyl CoA is synthesized within mitochondria, involving aerobic oxidation of glucose pyruvate, catabolism of certain amino acids, and β- Hydroxybutyrate Acetoacetate Acetyl CoA β- Oxidation. The sources of acetyl CoA include aerobic oxidation of sugars (glucose pyruvate) and fatty acids β- Oxidation, catabolism of certain amino acids, and oxidative breakdown of ketones. This indicates that acetyl CoA not only plays a core role in energy conversion, but also plays a crucial role in various metabolic pathways of cells.
Research Area TagsandCellMarkers , Cardiovascular , Metabolism
A-CoA(Acetyl Coenzyme A) ELISA Kit - procedures
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