CLIA Kit for Fibroblast Growth Factor 15 (FGF15) View larger

CLIA Kit for Fibroblast Growth Factor 15 (FGF15)

CC-CCL154Mu

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48T, 96T, 96T×5, 96T×10, 96T×100

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Data sheet

Size 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100
Applications Chemiluminescent immunoassay for Antigen Detection.
Detection Range 3.9-1,000pg/mL
Sensitivity The minimum detectable dose of this kit is typically less than 1.7pg/mL
Research Area Human gene deletion
Organism species Mus musculus (Mouse)
Item Name Fibroblast Growth Factor 15
Assay Length 2h
Method Competitive Inhibition
Sample Type serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Test Principle The microplate provided in this kit has been pre-coated with a monoclonal antibody specific to Fibroblast Growth Factor 15 (FGF15). A competitive inhibition reaction is launched between biotin labeled Fibroblast Growth Factor 15 (FGF15) and unlabeled Fibr
Assay procedure summary 1. Prepare all reagents, samples and standards
UniProt ID -

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Especificidad:

This assay has high sensitivity and excellent specificity for detection of Fibroblast Growth Factor 15 (FGF15).
No significant cross-reactivity or interference between Fibroblast Growth Factor 15 (FGF15) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibroblast Growth Factor 15 (FGF15) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Fibroblast Growth Factor 15 (FGF15) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Estabilidad:

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.

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