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ELISA Kit for Glutathione S Transferase (GST)
CC-SEX158Ge
Producto nuevo
Comprando este producto generará 7 Biopuntos. Su cesta contiene un total 7 Biopuntos puede ser convertido en un Biobonos Descuento 28.00EUR.
Hoja técnica
| Size | 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100 |
| Applications | Enzyme-linked immunosorbent assay for Antigen Detection. |
| Detection Range | 1.56-100ng/mL |
| Sensitivity | The minimum detectable dose of this kit is typically less than 0.57ng/mL |
| Organism species | Pan-species (General) |
| Alternative Names | GST-Tag |
| Item Name | Glutathione S Transferase |
| Assay Length | 3h |
| Method | Double-antibody Sandwich |
| Sample Type | biological fluids |
| Formato | 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100 |
| Test Principle | The microtiter plate provided in this kit has been pre-coated with an antibody specific to GST. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated antibody specific to GST. After TM |
| Assay procedure summary | 1. Prepare all reagents, samples and standards |
| UniProt ID | P08515 |
Más información
This assay has high sensitivity and excellent specificity for detection of Glutathione S Transferase (GST).
No significant cross-reactivity or interference between Glutathione S Transferase (GST) and analogues was observed.
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Glutathione S Transferase (GST) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Glutathione S Transferase (GST) 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.