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CE 99% Neutralizing Antibody Test Kit 25T / Box For Hospital

Categories Neutralizing Antibody Rapid Test
Brand Name: Aichek
Model Number: COVID-19-G02001A
Certification: CE
Place of Origin: China
MOQ: 5000 Test
Price: negotiable
Payment Terms: T/T
Supply Ability: negotiable
Packaging Details: 40box/carton
Storage: 2℃-30℃
User: Everyone
Accuracy: 99.05% (95% CI: 97.58%~99.63%)
Certificate: CE ISO 13485
Key words: Safe Reliable Economic
OEM: OEM customized packing avaliable
Formats: 25T/box 1T/box
Sample: Blood
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CE 99% Neutralizing Antibody Test Kit 25T / Box For Hospital

SARS-CoV-2 Neutralizing Antibody Test Kit For Hospital CE Certificate

For professional and in vitro diagnostic use only.

Product NameSARS-CoV-2 Neutralizing Antibody Test Kit For Hospital CE Certificate
FormatsStrip(3mm)Device(4mm) uncut sheet
Place of OrigenChina
SpecimenBlood
Read Time15 minutes
Shelf life2 years
Package25T/Box
Storage2℃-30℃

For professional and in vitro diagnostic use only.


2019nCov Ag Rapid Test Kit

SARS-Cov-2 Neutralising Antibody Kits
When someone contracts COVID-19, the host’s immune response can be measured by the presence of neutralising antibodies. Neutralising antibodies prevent the interaction between SARS-CoV-2 virus and receptors on human cells, giving the patient immunity.

Neutralising antibody detection is therefore very important in understanding and treating COVID-19. For example, to:

Test neutralising antibody induction during vaccine development, and how long antibodies are present for after infection
Confirm COVID-19 patient immunity
Allow donor selection in convalescent plasma therapy (using the antibodies of immune patients to help patients with active COVID-19)
Identify compounds that can interfere with the mechanism of viral infection, to prevent or treat COVID-19


[PERFORMANCE CHARACTERISTICS]


Sensitivity

The sensitivity to S-mIgG1 neutralizing antibody can reach 2ug/mL.

Accuracy

A side-by-side comparison was conducted by the results of SARS-Cov-2 Neutralizing Antibody Test Device (Test Reagent) developed by Hangzhou Deangel Biological Engineering Co., Ltd. and cPassTM from Genscript CO., Ltd. 328 clinical specimens from Professional Point of Care site were evaluated, 105 were positive and others negative. Base on the results from the clinical studies, the statistical analysis was made as follows:

cPassTMTotal
PositiveNegative

Test

reagent

Positive96298
Negative9221230
Total105223328

For test reagent, the clinical sensitivity with the “Compared Reagent” was 91.4% (95% CI: 77.7%~100%), the clinical specificity was 99.1% (95% CI: 97.2%~100%), the coincidence rate was 96.6% (95% CI: 92.4%~100%).

[SUMMARY]

The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.


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