CLIA Kit for Prothrombin Fragment 1+2 (F1+2)
Sizes: 24T, 48T, 96T
Catalogue Numbers: SCA710Ra-24, SCA710Ra-48, SCA710Ra-96
Citations, Manuals and MSDS Available upon request.
Featured Series: Sandwich kit
Target: Prothrombin Fragment 1+2
Target Species: Rat
Uniprot: P18292
Featured Series Function: Detects protein (regular version)
Specificity: Reactive with Rat F1+2 / Prothrombin Fragment 1+2
Method: Chemiluminescence
Detection principle: Double-antibody Sandwich
Detection
range: 0.55-400ng/mL
Sensitivity: 0.23ng/mL
Assay Time: 2h, 40min
Sample Size: 100uL
Recommended/Predicted
Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids
Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%
Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)
Shelf-life: 12 months
Specificity: This assay has high sensitivity and excellent specificity for detection of Prothrombin Fragment 1+2 (F1+2).
No significant cross-reactivity or interference between Prothrombin Fragment 1+2 (F1+2) and analogues was observed.
Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Prothrombin Fragment 1+2 (F1+2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Prothrombin Fragment 1+2 (F1+2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
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.
Target: 1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 100µL Substrate Solution. Incubate 10 minutes at 37°C;
8. Read RLU value immediately.
Test principle: The microtiter plate provided in this kit has been pre-coated with an antibody specific to F1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specifictoF2. Next,Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the F1+2 level in the sample or standard.
Research Use Only