Code | CSB-E08002r |
Size | 96T,5×96T,10×96T |
Price | Request a Quote |
Trial Size |
24T ELISA Kit Trial Size (Only USD$150/ kit) * Sample kit cost can be deducted as a $30 credit for each 96-assay kit of the same analyte and brand you subsequently purchase within six months until depleted. More details >> Interested in a trial size? Please leave a message below.
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Intra-assay Precision (Precision within an assay): CV%<8% | ||||||
Three samples of known concentration were tested twenty times on one plate to assess. | ||||||
Inter-assay Precision (Precision between assays): CV%<10% | ||||||
Three samples of known concentration were tested in twenty assays to assess. |
To assess the linearity of the assay, samples were spiked with high concentrations of rat bFGF in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. | ||||||
| Sample | Serum(n=4) | ||||
1:1 | Average % | 90 | ||||
Range % | 84-98 | |||||
1:2 | Average % | 94 | ||||
Range % | 91-102 | |||||
1:4 | Average % | 100 | ||||
Range % | 92-109 | |||||
1:8 | Average % | 93 | ||||
Range % | 86-98 |
The recovery of rat bFGF spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. | ||||||
Sample Type | Average % Recovery | Range | ||||
Serum (n=5) | 95 | 89-98 | ||||
EDTA plasma (n=4) | 94 | 90-100 |
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. | |||||||
ng/ml | OD1 | OD2 | Average | Corrected | |||
20 | 2.558 | 2.634 | 2.596 | 2.405 | |||
10 | 1.508 | 1.567 | 1.537 | 1.346 | |||
5 | 0.924 | 0.928 | 0.926 | 0.735 | |||
2.5 | 0.556 | 0.542 | 0.549 | 0.358 | |||
1.25 | 0.417 | 0.421 | 0.419 | 0.228 | |||
0.625 | 0.337 | 0.348 | 0.343 | 0.152 | |||
0.312 | 0.272 | 0.284 | 0.278 | 0.087 | |||
0 | 0.187 | 0.195 | 0.191 |
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The rat bFGF ELISA Kit is engineered for accurate measurement of rat bFGF levels from samples including serum, plasma, or tissue homogenates. It uses the Sandwich-ELISA mechanism in combination with the enzyme-substrate chromogenic reaction to measure the bFGF content in the sample. The color intensity is positively correlated with the bFGF content in the sample.
FGF2, also called bFGF, plays an important role in the regulation of cell growth and differentiation under physiological and pathological conditions. It is a potent pro-angiogenic factor. Many studies have shown that FGF2-FGFR signaling participates in several biological processes, including embryonic development, tissue regeneration, wound repair, and normal hematopoiesis. FGF2 exerts an important role in the proliferation of hemangioblasts in the early stages of development. It is also implicated in self-renewal, cell survival, and cell adhesion of human embryonic stem cells. Dysregulated FGF2-FGFR signaling has been found in cancer cells and may be involved in the pathogenesis of many kinds of cancer. Upregulation of FGF2 is related to poor prognosis in patients of many cancer types.
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