Igm Antibody Rapid Detection Test Kit Elisa Method Wholeblood Specimen

• Type: IVD Reagent
• Package: Not Customized
• Transport Package: Carton
• Specification: 58*33*36cm
• Trademark: Runmei
• Origin: China
• Production Capacity: 1000000kits/Month

Product Description

 Igm Antibody Rapid Detection Test Kit Elisa Method Wholeblood Specimen

CE,FDA,ISO9001,ISO13485,Name List of Medical Devices and Supplies Companies with Certification/Authorization
from other Countries,Certificate For Exportation Of Medical Products

Product parameter

composition:Enzyme Conjugate,Calibration Solution (S0-S5),20X Wash Buffer Concentrate,Substrate Reagent A,Substrate Reagent B,Stop Solution,Capture plate,Sealer,Instructions,Plastic Bag

Packing specification

96 tests / kit

Storage temperature: 2-8ºC

Period of validity:Tentatively 12 months

Intened use

Neutralizing Antibody Detection Kit(ELISA ) is an indirect enzyme-linked immunoassay (ELISA) for quantitative determination of Neutralizing Antibody in plasma or serum. This kit is used for assisted diagnosis.

Priciple of the assay

 Neutralizing Antibody Detection Kit(ELISA ) is a for rapid Nab (neutralizing antibody) screening, which can mimic the virus neutralization process. The kit contains two key components: the Horseradish peroxidase (HRP) conjugated recombinant fragment (HRP-RBD) and the human ACE2 receptor protein (hACE2). The protein-protein interaction between HRP-RBD and hACE2 can be blocked by neutralizing antibodies against  RBD.
First, the samples and controls are pre-incubated with the HRP-RBD to allow the binding of the circulating neutralization antibodies to HRP-RBD. The mixture is then added to the capture plate which is pre-coated with the hACE2 protein. The unbound HRP-RBD as well as any HRP-RBD bound to non-neutralizing antibody will be captured on the plate, while the circulating neutralization antibodies_HRP-RBD complexes remain in the supernatant and get removed during washing. After washing steps, TMB solution is added. By adding Stop Solution, the reaction is quenched. This final solution can be read at 450 nm in a microtiter plate reader. The absorbance of the sample is inversely dependent on the titer of the anti neutralizing antibodies.