IDK® Calprotectin ELISA

SKU KR6927 Category

$515.00

Product Specifications

Method: ELISA
Sample Type (Matrix): Stool
SAMPLE VOLUME:
15 mg
Species: Human
Incubation time: 1h 10m
Range: 13-840 ng/mL
Size: 96 wells
Regulatory Status: For research use only in the U.S. Not for use in diagnostic procedures.

Description

The IDK® Calprotectin ELISA is an enzyme immunoassay intended for the quantitative determination of calprotectin (MRP 8/14, S100A8/A9) in stool.

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

For Laboratory Professional Use Only.

The IDK® Calprotectin ELISA is compatible with our IDK Extract® Stool Sample Preparation System.

If your lab is testing at high volumes, this kit is also available in a customized bulk pack (20 plates)

This is the RUO version of Immundiagnostik part number K 6927.

Developed by Immundiagnostik AG.

Test Principle of the IDK® Calprotectin ELISA

The IDK® Calprotectin ELISA is designed for the quantitative determination of Calprotectin. The assay utilizes the two-site sandwich technique with two selected monoclonal antibodies that bind to human Calprotectin. Standards, controls, and diluted samples assayed for human Calprotectin are added to wells of microplate coated with a high affine monoclonal anti-human calprotectin antibody.

During the first incubation step, Calprotectin in the samples is bound by the immobilized antibody. Then a peroxidase-labeled conjugate is added to each well, and the following complex is formed: capture antibody – human Calprotectin – peroxidase conjugate.

Tetramethylbenzidine (TMB) is used as a substrate for peroxidase. Finally, an acidic stop solution is added to terminate the reaction. The color changes from blue to yellow. The intensity of the yellow color is directly proportional to the calprotectin concentration of the sample.

A dose-response curve of the absorbance unit (optical density, OD at 450 nm) vs. concentration is generated using the values obtained from the standard. The presence of Calprotectin in the samples is determined directly from this curve.

 

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