IDK® Zonulin ELISA (Stool)

SKU KR5600 Categories ,

$850.00

In stock

Product Specifications

MethodELISA
Sample Type (Matrix)Stool
Sample Volume15 mg
SpeciesHuman
Incubation Time2h 10m
Range0.25 - 16 ng/mL
Size96 wells
Regulatory StatusFor research use only. Not for use in diagnostic procedures.

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Description

The IDK® Zonulin ELISA (Stool) is intended for the quantitative determination of zonulin in stool to assess intestinal permeability.

For research use only. Not for use in diagnostic procedures.

For Laboratory Professional Use Only.

If you’re in Canada, we offer a Health Canada Licensed version of this kit: K5600

Manufactured by Immundiagnostik AG.

Also available:

  • Zonulin ELISA Bulk Pack (Stool, 20 Plates): KR5600.20
  • Zonulin ELISA Bulk Pack (Serum, 20 Plates): KR5601.20
  • Zonulin ELISA (Serum): KR5601
  • Zonulin ELISA (Serum, Health Canada): K5601

Test Principle of the IDK® Zonulin ELISA (Stool)

The IDK® Zonulin ELISA (Stool) is based on the method of competitive ELISA.

As a first preparation step, biotinylated zonulin is added to the samples, standards, and controls. Afterward, aliquots of the treated samples, standards, and controls are transferred and incubated in microtiter plate wells coated with polyclonal anti-zonulin antibodies. During the incubation, the free target antigen in the samples competes with the biotinylated zonulin for the binding of the polyclonal anti-zonulin antibodies immobilized on the microtiter plate wells. The unbound components are removed by a washing step.

During a second incubation step, peroxidase-labeled streptavidin, which binds to the biotinylated zonulin, is added to each microtiter well. After a washing step to remove the unbound components, the peroxidase substrate tetramethylbenzidine is added.

Finally, the enzymatic reaction is terminated by an acidic stop solution. The color changes from blue to yellow, and the absorbance is measured in the photometer at 450 nm. The intensity of the yellow color is inversely proportional to the zonulin concentration in the sample; this means a high zonulin concentration in the sample reduces the concentration of the biotinylated zonulin bound to the immobilized anti-zonulin antibodies and lowers the photometric signal.

A dose-response curve of absorbance unit (optical density, OD at 450 nm) vs. concentration is generated using the values obtained from the standard.

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