CC-HEA710Hu
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Comprando este producto generará 7 Biopuntos. Su cesta contiene un total 7 Biopuntos puede ser convertido en un Biobonos Descuento 28.00EUR.
Size | 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100 |
Storage Conditions | -20°C |
Shipping Conditions | Entre 4°C y 8°C |
Applications | Enzyme-linked immunosorbent assay for Antigen Detection. |
Detection Range | 0.11-80pg/mL |
Sensitivity | The minimum detectable dose of this kit is typically less than 0.04pg/mL |
Organism species | Homo sapiens (Human) |
Item Name | Prothrombin Fragment 1+2 |
Assay Length | 3h |
Method | Double-antibody Sandwich |
Sample Type | Serum, plasma and other biological fluids |
Formato | 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100 |
Test Principle | The microplate provided in this kit has been pre-coated with an antibody specific to F1. Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to F2. Next, Avidin conjugated to Horseradish Perox |
Assay procedure summary | 1. Prepare all reagents, samples and standards |
UniProt ID | P00734 |
This assay has high sensitivity and excellent specificity for detection of High Sensitive Prothrombin Fragment 1+2 (F1+2).
No significant cross-reactivity or interference between High Sensitive Prothrombin Fragment 1+2 (F1+2) and analogues was observed.
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level High Sensitive 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 High Sensitive Prothrombin Fragment 1+2 (F1+2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
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.