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HK373 HUMAN COAGULATION FACTOR XII ELISA KITPRODUCT INFORMATION & MANUALRead carefully prior to starting procedures!ATTENTION For use in laboratory research only Not for clinical or diagnostic usewww.hycultbiotech.com
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01
Prepare all necessary materials including the complement factor D ELISA kit, samples, standards, and reagents.
02
Thaw the components of the kit and samples to room temperature.
03
Label the microtiter plate wells according to the samples and standards to be tested.
04
Add the standards and samples to the appropriate wells.
05
Add the enzyme conjugate to all wells.
06
Incubate the plate for a specific amount of time at the recommended temperature.
07
Wash the plate to remove unbound substances.
08
Add the substrate solution and incubate for a specific time.
09
Stop the reaction by adding the stop solution.
10
Measure the absorbance of each well using a microplate reader and calculate the concentrations of complement factor D in the samples.

Who needs complement factor d elisa?

01
Individuals suspected of having deficiencies in complement factor D.
02
Researchers studying the role of complement factor D in various diseases.
03
Healthcare providers monitoring the progression of certain conditions.
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Complement factor D ELISA is a laboratory test designed to measure the levels of complement factor D in a patient's serum or plasma, which is involved in the immune response.
Individuals or healthcare providers who need to assess complement factor D levels for diagnosing certain immune-related conditions are typically required to file for complement factor D ELISA.
Filling out a complement factor D ELISA test involves collecting blood samples, preparing the samples according to the kit instructions, and then following the provided protocol for the assay.
The purpose of complement factor D ELISA is to evaluate the immune system's functionality and to aid in the diagnosis of conditions associated with complement pathway deficiencies.
Information that must be reported includes patient identification details, sample type, assay results, reference ranges, and any relevant clinical information.
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