DEMO – Quanticon™ Rat IFN-γ

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This kit uses the Sandwich-ELISA principle. The microtiter plate strips has been pre-coated with an affinity purified antibody to Rat IFN-γ. Standards or samples containing Rat IFN-γ are added to the plate and reacted with capture antibody. A second anti-Rat IFN-γ antibody labeled biotin is then added and binds to Rat IFNγ captured on the plate. After that, Streptavidin-Horseradish Peroxidase(SA-HRP) is added to form a sandwich complex of solid phase antibody-Rat IFN-γ-biotin labeled antibody-SA-HRP. And then, TMB substrate solution is added to all wells and incubated. An enzyme-catalyzed reaction generates a blue color in the solution, thereafter, stop solution is added to stop the substrate reaction and the color turns yellow. The yellow solution is read at a wavelength of 450nm. The concentration of Rat IFN-γ in the samples is then calculated from the OD value by establishing a standard curve.

Cat no:

ABQ-ES96-IFNΓrt
ABQ-ES96-IFNΓrt
Size:

Rate
Rate
96T:

$450
$450
48T:

$230
$230

Datasheet


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MS/DS


COA




Product name Quanticon™ Rat IFN-γ(Interferon Gamma) ELISA Kit
SKUABQ-ES96-IFNΓrt
ApplicationsELISA
ReactivityRAT
Sensitivity10 pg/mL.
Detection Range31.25-2500pg/mL.
Sample TypeSerum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids
Sample Volume100 μL
Assay TypeSandwich
Assay Duration3.5H
Detection Wavelength450nm
Storage2-8oC/-20 oC

Citations

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.

Product name Quanticon™ Rat IFN-γ(Interferon Gamma) ELISA Kit
SKUABQ-ES96-IFNΓrt
ApplicationsELISA
ReactivityRAT
Sensitivity10 pg/mL.
Detection Range31.25-2500pg/mL.
Sample TypeSerum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids
Sample Volume100 μL
Assay TypeSandwich
Assay Duration3.5H
Detection Wavelength450nm
Storage2-8oC/-20 oC

Citations

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.