Instant ELISA Kit for Androstenedione (ASD)
- Product No.IEA456Ge
- Organism SpeciesPan-species (General) Same name, Different species.
- Sample Typen/a
- Test MethodCompetitive Inhibition
- Assay Length1h, 10min
- Detection Rangen/a
- UOM 48T96T 96T*5 96T*10 96T*100
For more details, please contact local distributors! US$ 1194
For more details, please contact local distributors! US$ 5373
For more details, please contact local distributors! US$ 10149
For more details, please contact local distributors! US$ 83580
For more details, please contact local distributors!
This assay has high sensitivity and excellent specificity for detection of Instant Androstenedione (ASD).
No significant cross-reactivity or interference between Instant Androstenedione (ASD) and analogues was observed.
Matrices listed below were spiked with certain level of Instant Androstenedione (ASD) and the recovery rates were calculated by comparing the measured value to the expected amount of Instant Androstenedione (ASD) in samples.
|Matrix||Recovery range (%)||Average(%)|
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Instant Androstenedione (ASD) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Instant Androstenedione (ASD) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Instant Androstenedione (ASD) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
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
|Pre-coated, ready to use 96-well strip plate||1||Plate sealer for 96 wells||4|
|Detection Reagent A||1×120µL||Assay Diluent A||1×12mL|
|TMB Substrate||1×9mL||Stop Solution||1×6mL|
|Wash Buffer (30 × concentrate)||1×20mL||Instruction manual||1|
Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 30 minutes at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 30 minutes at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 10 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
|Plos One||Association between Polycystic Ovary Syndrome and Cavia (Guinea pig )t Microbiota Pubmed:27093642|
|Scientific Reports||Molecular characterization of insulin resistance and glycolytic metabolism in the rat uterus pubmed:27461373|
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