产品详情
组分(Materials Provided)
IDComponentsSizeRAS034-C01Pre-coated Human ACE2 Microplate1 plateRAS034-C02Positive Control100 μLRAS034-C03Negative Control100 μLRAS034-C04HRP-SARS-CoV-2 Spike RBD(P.1)15 μgRAS034-C0510xWashing Buffer50 mLRAS034-C06Dilution Buffer50 mLRAS034-C07Substrate Solution12 mLRAS034-C08Stop Solution7 mL产品概述(Product Overview)
It's been reported that coronavirus can infect the human respiratory epithelial cells through interaction with the human ACE2 receptor. The spike protein is a large type I transmembrane protein containing two subunits, S1 and S2. S1 mainly contains a receptor binding domain (RBD), which is responsible for recognizing the cell surface receptor. S2 contains basic elements needed for the membrane fusion.The S protein plays key parts in the induction of neutralizing-antibody and T-cell responses, as well as protective immunity.
应用说明(Application)
This kit is developed for qualitative detection or titer measurement of Anti-SARS-CoV-2 (P.1) neutralizing antibody (Spike RBD) in human serum.
It is for research use only.
存储(Storage)
2-8℃
原理(Assay Principles)
This assay kit is used to measure the levels of Anti-SARS-CoV-2 neutralizing antibody through a competitive ELISA. The microplate in the kit has been pre-coated with Human ACE2 protein. First serum samples, Positive control, Negative Control are added to the wells followed by addition of HRP-SARS-CoV-2 Spike RBD. After incubation, the wells are washed and substrate is added to the wells. The reaction is terminated by the addition of stop solution and the intensity of color is measured at 450 nm. The presence of neutralizing antibodies in samples will compete with ACE2 for HRP-SARS-CoV-2 Spike RBD binding. The intensity of assay signal decrease proportionally to the presence of Anti-SARS-CoV-2 neutralizing antibody.
Your experiment will include 5 simple steps:
a) All reagents were returned to room temperature (20°C-25°C) before use.
b) Make series the tested sample and control with ditlution buffer, HRP-SARS-CoV-2 Spike RBD diluted with dilution buffer.
c) Add the diluted sample, Control and the HRP-SARS-CoV-2 Spike RBD add the plate respectively.
d) Wash the plate and add TMB or other colorimetric HRP substrate.
e) Stop the substrate reaction by add diluted acid. Absorbance (OD) is calculated as the absorbance at 450 nm minus the absorbance at 630 nm to remove background prior to statistical analysis. The OD Value reflects the amount of antibody bound.
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