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The kit is used for qualitative detection of novel coronal virus
neutralizing antibodies in human serum, plasma and whole blood
samples.
Corona beer is long. A new corona virus belonging to corona
viruses. May cause viral pneumonia, the main clinical symptoms are
fever, tiredness, dry cough. There are also patients with nasal
congestion, runny nose, sore throat and diarrhea. Severe illness
usually follows one week with dyspnea and/or hypoxemia, acute
dyspnea syndrome, septic shock, refractory metabolic adoxis, and
coagulation dysfunction.
New coronavirus infections or vaccinations in 2019 can cause an
immune response that produces antibodies in the blood. Secreted
antibodies protect against viral infection. After infection, they
remain in the human circulatory system for months to years, where
they bind quickly and firmly to the pathogen and prevent the virus
from replicating. These antibodies are called neutralizing
antibodies. Neutralization antibody test can determine whether a
person has the ability to prevent viral infection.
Imo chromaticity photography is used for supporting components. The
test card includes quality control line C, test line T and
reference line R. Detection of upward diffusion loading and binding
of capillary samples (serum/plasma and whole blood) as well as
detection of NC membrane protein and signal of s-RBD manufacturer
plate position line of immobilized ACE2. When neutralizing
antibodies are present in the sample, they bind to the labeled
S-RBD antigen when passing through the labeled S-RBD antigen.
Neutralizing antibodies prevent S-RBD from binding to ACE2. As a
result, the amount of neutralizing antibodies and the negative
correlation signal value are reduced. At very high concentrations
of neutralizing antibodies, the T-line becomes colorless. Whether
reference lines R and QCC are colored for T lines. Use quality
control line C
If the C line is not colored, the test is invalid and the sample
needs to be tested again.
The kit consists of test cards and sample buffers.
Test card: aluminum foil bag, desiccant, test strip, plastic card
composition. The test paper consists of absorption paper,
nitrocellulose film, sample pad, binding pad and rubber sheet. T
line (test line) of nitrifying membrane covers ACE2 protein, C line
(QC line) covers Ab of QC line, R line (reference line) covers
reference Ab, and solder pad contains label 2019nCoVAb.
Sample buffer: phosphoric acid, sodium nitrite, etc.
The storage temperature is 2℃ ~ 30℃ and the validity period is 12
months.
The aluminum foil bag is valid for one hour.
Production Lot Number: Refer to the label for details.
Expiry date: Please see the label for details.
1. Collect serum, plasma or whole blood samples.
2. Sediment and plankton in the sample will affect the experimental
results, so it needs to be removed by centrifugation.
3. Anti-coagulant: loofah anti-coagulant, EDA anti-coagulant,
sodium citrate anti-coagulant are not obvious.
4. Blood collection by experts is needed. Serum/serum/plasma tests
are recommended. In emergency or special circumstances, a patient's
whole blood sample can also be used for rapid testing.
5. Serum and plasma samples should not be stored for more than 8
hours at room temperature.
It can be stored for 5 days at 2-8 ℃ and 6 months below -20℃, but
please avoid repeated freezing and melting. Whole blood samples do
not freeze and need to be stored at 2℃ to 8℃ for 48 hours.
Please read the instructions carefully before testing. All reagents
must be returned to room temperature prior to test. Tests must be
carried out at room temperature.
1. Take the test card out of the box and use it within 1 hour.
2. Add 20L sample (serum, plasma or whole blood) to the filling
hole of the test card, add 2 drops (~ 60L) of sample buffer memory
and start timing.
3. After 10 to 15 minutes of reaction at room temperature, read the
results. Invalid after 20 minutes.
Test card description:
1. Invalid result: Quality management line (Line C) is invalid and
needs to be tested again.
2. Negative result: The appearance color of test line (T line) is
greater than that of reference line (R line), quality management
line (C line) and reference line (R line).
3. Positive results: red watchband test line (T line) or red
watchband, test line (T line) for the baseline line (R line) and
quality management (C) line and baseline line (R line) color
distinction.
This kit is used for qualitative analysis, but only for Invitro
assisted diagnosis.
2. Please add appropriate test samples. If the sample size is too
large or too small, the result may be incorrect.
3. Hemolysis, lipids in the blood, jaundice, sample contamination,
etc., may affect the test results, so it must be avoided as far as
possible.
4. The test results of the reagent are for clinical reference only,
and should not be used as the sole basis for clinical diagnosis and
treatment. The final diagnosis of the disease is made by combining
all clinical and examination results.
1. This product is only used for Invitro diagnosis.
This product is disposable and can't be reused.
3. Please read the instructions carefully before operation, and
strictly follow the instructions of reagent for experimental
operation.
4. Please avoid conducting the experiment under harsh environmental
conditions (84 disinfectants, sodium hypochlorite, acid, alkali,
acetaldehyde, other corrosive gases with high concentration, dust,
etc.). Laboratory disinfection needs to be carried out after the
experiment.
5. All samples and reagents used shall be considered as potentially
infectious substances and shall be disposed of in accordance with
local regulations.
6. The reagent must be used within the expiry date stated on the
package. To prevent moisture, the test card needs to be removed
from the aluminum foil bag as soon as possible after removal.
Do not re-use | Store at 2℃~30℃ | ||
Consult instructions for use | In vitro diagnostic medical device | ||
Batch code | Use-by date | ||
Keep dry | Keep away from sunlight | ||
Authorized representative in the European Community | Manufacturer |