ArtNr |
CEK644Ge-24T |
Hersteller |
Cloud-Clone
|
Menge |
24T |
Kategorie |
|
Typ |
Elisa |
Specific against |
other |
Sensitivity |
The minimum detectable dose of this kit is typically less than 367pg/mL |
ECLASS 10.1 |
32160605 |
ECLASS 11.0 |
32160605 |
UNSPSC |
41116126 |
Alias |
Ciclosporin; Cyclosporine; Cyclosporin |
Lieferbar |
|
Specificity |
This assay has high sensitivity and excellent specificity for detection of Cyclosporin A (CsA). No significant cross-reactivity or interference between Cyclosporin A (CsA) and analogues was observed. |
Manufacturers Category |
ELISA Kit |
Application |
Enzyme-linked immunosorbent assay for Antigen Detection. |
Organism species |
Pan-species (General) |
Sample type |
serum, plasma other biological fluids |
Assay length |
2h |
Method |
Competitive Inhibition |
Precision |
Intra-assay: CV<10% Inter-Assay: CV<12% |
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. |
Assay procedure summary |
1. Prepare all reagents, samples and standards; 2. Add 50uL standard or sample to each well. uuuuAnd then add 50uL prepared Detection Reagent A immediately. uuuuShake and mix. Incubate 1 hour at 37°C; 3. Aspirate and wash 3 times; 4. Add 100uL prepared Detection Reagent B. Incubate 30 minutes at 37°C; 5. Aspirate and wash 5 times; 6. Add 90uL Substrate Solution. Incubate 10-20 minutes at 37°C; 7. Add 50uL Stop Solution. Read at 450 nm immediately. |
Test principle |
This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Cyclosporin A (CsA) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Cyclosporin A (CsA) and unlabeled Cyclosporin A (CsA) (Standards or samples) with the pre-coated antibody specific to Cyclosporin A (CsA). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Cyclosporin A (CsA) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Cyclosporin A (CsA) in the sample. |
Item Name |
Cyclosporin A |
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