Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

This kit uses the Sandwich-ELISA principle. The microtiter plate strips has been precoated with an affinity purified antibody to Rat IL-33. Standards or samples containing Rat IL-33 are added to the plate and reacted with capture antibody. A second anti-Rat IL-33 antibody labeled biotin is then added and binds to Rat IL-33 captured on the plate. After that, Streptavidin-Horseradish Peroxidase (SA-HRP) is added to form a sandwich complex of solid phase antibody-Rat IL-33-biotin labeled antibody-SA-HRP.And then, TMB substrate solution is added to all wells and incubated. An enzymecatalyzed 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 IL-33 in the samples is then calculated from the OD value by establishing a standard curve.

Cat no: ABQ-ES96-IL33rt
ABQ-ES96-IL33rt
Size: Rate
Rate
96T: $450
$450
48T: $230
$230

Product name

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

SKU

ABQ-ES96-IL33rt

Applications

ELISA

Reactivity

RAT

Sensitivity

1.0 pg/mL.

Detection Range

50-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

Citations

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

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

elisa-kit-images-e1737629308569-removebg-preview
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This kit uses the Sandwich-ELISA principle. The microtiter plate strips has been precoated with an affinity purified antibody to Rat IL-33. Standards or samples containing Rat IL-33 are added to the plate and reacted with capture antibody. A second anti-Rat IL-33 antibody labeled biotin is then added and binds to Rat IL-33 captured on the plate. After that, Streptavidin-Horseradish Peroxidase (SA-HRP) is added to form a sandwich complex of solid phase antibody-Rat IL-33-biotin labeled antibody-SA-HRP.And then, TMB substrate solution is added to all wells and incubated. An enzymecatalyzed 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 IL-33 in the samples is then calculated from the OD value by establishing a standard curve.

Cat no: ABQ-ES96-IL33rt ABQ-ES96-IL33rt Size: Rate Rate 96T: $450 $450 48T: $230 $230 Datasheet Get Quote MS/DS COA

Product name

Quanticon™ Rat IL-33(Interleukin 33) ELISA Kit

SKU

ABQ-ES96-IL33rt

Applications

ELISA

Reactivity

RAT

Sensitivity

1.0 pg/mL.

Detection Range

50-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

Detection Wavelength

450nm

Storage

2-8oC/-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 IL-33(Interleukin 33) ELISA Kit

SKU

ABQ-ES96-IL33rt

Applications

ELISA

Reactivity

RAT

Sensitivity

1.0 pg/mL.

Detection Range

50-1000pg/mL.

Sample Type

Serum, Plasma, Tissue homogenate, Cell lysates and Cell culture supernatant and other biological fluids

Sample Volume

100 ÎĽL

Assay Type

Sandwich

Assay Duration

3.5H

Detection Wavelength

450nm

Storage

2-8oC/-20 oC

Citations

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

Principle of the Procedure

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig CCK. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig CCK. 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 Pig CCK in the samples is then determined by comparing the OD of the samples to the standard curve.

Citations  Â