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CLIA Kit for Adenosine Triphosphate (ATP)
Adenosine-5'-Triphosphate
- Product No.CCA349Ge
- Organism SpeciesPan-species (General) Same name, Different species.
- Sample TypeSerum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
- Test MethodCompetitive Inhibition
- Assay Length2h
- Detection Range3.9-1,000ng/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 1.5ng/mL.
- DownloadInstruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
- FOB
US$ 669
For more details, please contact local distributors! US$ 955 US$ 4298 US$ 8118 US$ 66850
Specificity
This assay has high sensitivity and excellent specificity for detection of Adenosine Triphosphate (ATP).
No significant cross-reactivity or interference between Adenosine Triphosphate (ATP) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of Adenosine Triphosphate (ATP) and the recovery rates were calculated by comparing the measured value to the expected amount of Adenosine Triphosphate (ATP) in samples.
Matrix | Recovery range (%) | Average(%) |
serum(n=5) | 91-105 | 101 |
EDTA plasma(n=5) | 98-105 | 102 |
heparin plasma(n=5) | 78-98 | 85 |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Adenosine Triphosphate (ATP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Adenosine Triphosphate (ATP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Adenosine Triphosphate (ATP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample | 1:2 | 1:4 | 1:8 | 1:16 |
serum(n=5) | 83-101% | 83-96% | 88-102% | 81-89% |
EDTA plasma(n=5) | 78-98% | 90-97% | 94-101% | 90-97% |
heparin plasma(n=5) | 82-93% | 94-103% | 89-103% | 78-90% |
Stability
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Reagents and materials provided
Reagents | Quantity | Reagents | Quantity |
Pre-coated, ready to use 96-well strip plate | 1 | Plate sealer for 96 wells | 4 |
Standard | 2 | Standard Diluent | 1×20mL |
Detection Reagent A | 1×120µL | Assay Diluent A | 1×12mL |
Detection Reagent B | 1×120µL | Assay Diluent B | 1×12mL |
Substrate A | 1×10mL | Substrate B | 1×2mL |
Wash Buffer (30 × concentrate) | 1×20mL | Instruction manual | 1 |
Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 100µL Substrate Solution. Incubate 10 minutes at 37°C;
7. Read RLU value immediately.
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Magazine | Citations |
Iranian Journal of Health and Physical activity | Effects of Aerobic Training, with or without Zizyphus Jujuba Water Extraction, on Fundus Nesfatin-1, ATP, HDL-C, and LDL-C Concentrations in Female Rats Ijvst: Source |
Journal of Neurochemistry | Neuroprotective effects of vildagliptin in rat rotenone Parkinson's disease model: role of RAGE‐NFκB and Nrf2‐antioxidant signaling pathways PubMed: 25752913 |
American Journal of Animal and Veterinary Sciences | Metabolic Features of Heart Failure with Different Etiology ofsp11075 |
toxicology in vitro | Rifampicin-induced injury in L02 cells is alleviated by 4-PBA via inhibition of the PERK-ATF4-CHOP pathway. pubmed:27470132 |
Free radical biology and medicine | Rifampicin-induced injury in HepG2 cells is alleviated by TUDCA via increasing bile acid transporters expression and enhancing the Nrf2-mediated adaptive response. pubmed:28688954 |
Dipòsit Digital de la Universitat de Barcelona | Chemiluminescent bioanalytical assays for clinical biomarkers 2445/116053 |
Evidence-Based Complementary and Alternative Medicine | The Antioxidative Action of ZTP by Increasing Nrf2/ARE Signal Pathway |
Antihypoxic and anti-ischemic properties of the North Caucasus flora plant extracts | |
Respiratory Physiology & Neurobiology | Effects of nanoparticles on Neuroinflammation in a Mouse Model of Asthma Pubmed: 31542455 |
Journal of Cosmetic Dermatology | Novel complex of cosmetic ingredients with promising action in preventing hair loss and follicular aging through mechanism involving enrichment of WNT/signaling … Pubmed: 33179848 |
Bangladesh Journal of Pharmacology | Ethylmethylhydroxypyridine succinate, acetylcysteine and choline alphoscerate improve mitochondrial function under condition of cerebral ischemia in rat |
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | Prostaglandin E receptor subtype 4 protects against diabetic cardiomyopathy by modulating cardiac fatty acid metabolism via FOXO1/CD36 signalling 33647796 |
Serum Metabolomic Analysis of Coronary Heart Disease Patients with Stable Angina Pectoris Subtyped by Traditional Chinese Medicine Diagnostics Reveals ¡ | |
Neurourol Urodyn | Estrogen inhibits bladder overactivity in rats with cyclophosphamide‐induced cystitis via downregulating the expression of P2X3 receptors in bladder epithelium cells 34622458 |
Biomed Res Int | A Famous Chinese Medicine Formula: Yinhuo Decoction Antagonizes the Damage of Corticosterone to PC12 Cells and Improves Depression by Regulating … Pubmed:35281603 |
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