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ELK5280-48T, Mouse MSTN(Myostatin) ELISA Kit, 48T
2.178,00 RON
Mouse MSTN(Myostatin) ELISA Kit
SKU
ELK5280-48T
Alternative Names: GDF8; Growth Differentiation Factor 8
Species: Mouse
Assay Type: Competitive Inhibition
Sensitivity: 253.7 pg/mL
Standard: 50000 pg/mL
Detection range: 781.25-50000 pg/mL
Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length: 2h
Research Area: Cytokine;Metabolic pathway;Bone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse MSTN protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse MSTN. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse MSTN in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 1.800,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: GDF8; Growth Differentiation Factor 8 Species: Mouse Assay Type: Competitive Inhibition Sensitivity: 253.7 pg/mL Standard: 50000 pg/mL Detection range: 781.25-50000 pg/mL Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids Assay length: 2h Research Area: Cytokine;Metabolic pathway;Bone metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse MSTN protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse MSTN. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse MSTN in the samples is then determined by comparing the OD of the samples to the standard curve. |
