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CircuLexTMHuman MICA ELISA Kit Users Manual For Research Use Only, Not for use in diagnostic proceduresELISA Kit for Measuring Human MICACircuLex Human MICA ELISA Kit Cat# CY8206 Intended Use................................................
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How to fill out circulex human mica elisa

01
Thaw the CircuLex Human MICA ELISA kit components to room temperature before starting the assay.
02
Dilute the standards, controls, and samples in the appropriate diluent provided in the kit.
03
Add the diluted standards, controls, and samples to the appropriate wells of the microtiter plate coated with capture antibodies.
04
Incubate the plate at the specified temperature for the recommended time.
05
Wash the plate to remove unbound substances.
06
Add the detection antibody and incubate the plate again.
07
Wash the plate and add the substrate solution to develop color.
08
Stop the reaction by adding the stop solution.
09
Read the plate at the specified wavelength and calculate the concentrations of MICA in the samples using the standard curve.

Who needs circulex human mica elisa?

01
Researchers studying the expression of MICA in human samples.
02
Medical professionals monitoring MICA levels in patients with certain diseases or conditions.
03
Laboratories conducting research on immune responses and tumor immunology.
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Circulex Human Mica ELISA is a type of enzyme-linked immunosorbent assay (ELISA) used for detecting specific antibodies or antigens in human serum, aiding in the diagnosis of various medical conditions.
Healthcare providers and laboratories performing the Circulex Human Mica ELISA test are typically required to file results and relevant documentation.
To fill out the Circulex Human Mica ELISA, follow the provided testing protocol, ensuring proper sample collection, reagent preparation, and adherence to controls, followed by documenting results in a specified format.
The purpose of Circulex Human Mica ELISA is to diagnose specific diseases by detecting the presence of particular antibodies or antigens in blood samples.
Reported information typically includes patient identification details, test results, specimen type, date of testing, and any relevant clinical information.
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