Monkeypox Virus rapid test kit 2022 MPV Nucleic Acid Detection Kit PCR Test
| Brand |
Testsealabs |
| Certification: |
CE |
| OEM |
Available |
| Sample type |
throat swabs and nasal swab |
| High sensitivity |
LOD:500copies/mL |
| High specificity |
No cross-reactivity with other pathogens |
| Convenient detection |
67min amplification |
| Non-closed equipment required |
Any of real-time PCR instruments with FAM and VIC |
[ INTRODUCTION ]
*The kit is used for in vitro qualitative detection of suspected cases of Monkeypox Virus (MPV), clustered cases and other cases that *need to be diagnosed for Monkeypox Virus infection.
*The kit is used to detect the f3L gene of the MPV in throat swabs and nasal swab samples.
*The test results of this kit are for clinical reference only and should not be used as the sole criterion for clinical diagnosis. It is recommended to conduct a comprehensive analysis of the condition based on the patient's clinical manifestations and other laboratory tests. 
[ PRODUCT FEATURE ]
[ Principle ]
This kit takes the specific conserved sequence of the MPV f3L gene as the target region. The real-time fluorescence quantitative PCR technology and nucleic acid rapid release technology are used to monitor the viral nucleic acid through the change of fluorescence signal of amplification products. The detection system includes internal quality control, which is used to monitor whether there are PCR inhibitors in the samples or whether the cells in the samples are taken, which can effectively prevent the false negative situation.
[ MAIN COMPONENTS ]
The kit contains reagents for processing 48 tests or quality control, including the following components:
Reagent A
| Name |
Main components
|
Quantity
|
MPV detection
reagent
|
The reaction tube contains Mg2+,
f3L gene /Rnase P primer probe,
reaction buffer, Taq DNA enzyme.
|
48 tests |
Reagent B
| Name |
Main components
|
Quantity
|
MPV
Positive Control
|
Containing MPV target fragment
|
1 tube
|
MPV
Negative Control
|
Without MPV target fragment
|
1 tube
|
DNA release reagent
|
The reagent contains Tris, EDTA
and Triton.
|
48pcs |
Reconstitution reagent
|
DEPC treated water
|
5ML |
Note: The components of different batch numbers cannot be used interchangeably
[ Storage Conditions And Shelf Life ]
1.Reagent A/B can be stored at 2-30°C, and the shelf life is 10 months.
2.Please open the test tube cover only when you are ready for the test.
3.Do not use test tubes beyond the expiration date.
4.Do not use a leaking detection tube.
[ Applicable Instrument ]
Suitable for Suitable for LC480 PCR analysis system, Gentier 48E Automatic PCR analysis system, ABI7500 PCR analysis system.
[ Sample Requirements ]
1.Applicable sample types: throat swabs samples.
2.Sampling solution: After verification, it is recommended to use normal saline or Virus preservation tube produced by Hangzhou Testsea biology for sample collection.
throat swab: wipe bilateral pharyngeal tonsils and posterior pharyngeal wall with disposable sterile sampling swab, immerse the swab into the tube containing 3mL sampling solution, discard the tail, and tighten the tube cover.
3.Sample storage and delivery: The samples to be tested should be tested as soon as possible. The transportation temperature should be kept at 2~8ºC.The samples that can be tested within 24 hours can be stored at 2ºC~8ºC and if the samples cannot be tested within 24 hours, it should be stored at less than or equal to -70ºC (if there is no storage condition of -70ºC, it can be stored at -20ºC temporarily), avoid repeated
freezing and thawing.
4.Proper sample collection, storage, and transportation are critical to the performance of this product.
[Testing Method ]
1.Sample processing and sample addition
1.1 Sample processing
After mixing the above sampling solution with samples, take 30μL of the sample into the DNA release reagent tube and mix it evenly.
1.2 Loading
Take 20μL of the reconstitution reagent and add it to the MPV detection reagent, add 5μL of the above processed sample (The positive control and negative control shall be processed in parallel with the samples), cover the tube cap, centrifuge it at 2000rpm for 10 seconds.
2. PCR amplification
2.1 Load the prepared PCR plate/tubes to the fluorescence PCR instrument, Negative control and positive control shall be set for each test.
2.2 Fluorescent channel setting:
1)Choose FAM channel for MPV detection;
2)Choose HEX/VIC channel for internal control gene detection;
3.Results analysis
Set the base line above the highest point of the negative control's fluorescent curve.
4.Quality control
4.1 Negative control:No Ct value detected in FAM,HEX/VIC channel, or Ct>40;
4.2 Positive control:In FAM,HEX/VIC channel, Ct≤40;
4.3 The above requirements should be satisfied in the same experiment, otherwise the test results are invalid and the experiment needs to be repeated.
[ Cut off value ]
A sample is considered as positive when: Target sequence Ct≤40, The internal control gene Ct≤40.
[ Results interpretation ]
Once the quality control is passed, users should check if there is an amplification curve for each sample in HEX/VIC channel, if there is and with Ct≤40, it indicated the internal control gene is successfully amplified and this particular test is valid. Users can proceed to the follow up analysis:
3.For samples with the amplification of internal control gene failed (HEX/VIC
channel, Ct>40,or no amplification curve), low Viral load or the existence of PCR inhibitor could be the reason of failure, the examination should repeated from the specimen collection;
4.For positive samples and cultured virus, the results of internal control do not affect;
For samples tested negative, the internal control needs to be tested positive otherwise the overall result is invalid and the examination needs to be repeated, starting from the specimen collection step
[ Packing&Transportation ]
[ About us ]
Audited Supplier 
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