Novel Coronavirus (2019-nCoV) Real-time RT-PCR Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the 2019-nCoV in oropharyngeal swabs and bronchoalveolar lavage fluid collected from individuals suspected of COVID-19 by their healthcare provider.
One Step Test for SARS-CoV-2 Antigen (Colloidal Gold) is intended for the qualitative detection of nucleocapsid protein antigen from SARS-in serum, plasma or whole blood samples from patients suspected of COVID-19 infection by a healthcare provider.
A kit contains:
Package specifications: 25 tests/box
1) Getein SARS-CoV-2 antigen test card in a sealed pouch with desiccant
2) Sample extraction solution: 25 tubes/box
3) Sampling swab: 25 pieces/box
4) Disposable pipette: 25 pieces/box
5) User manual: 1 piece/box
[Intended Usage]
This kit is used for the in vitro qualitative detection of suspected cases of pneumonia caused by New Coronavirus infection, patients with suspected clusters, other patients who need to be diagnosed or differentially diagnosed with the New Coronavirus infection, and nasopharyngeal swabs, oropharyngeal swabs, and bronchoalveolar lavage fluid samples of patients with mutation beads for the New Coronavirus ORF1ab and N gene, S gene N501Y mutation and S gene E484K mutation sites.
[Storage Conditions & Validity]
1. The kit should be stored frozen at -20 and protected from light; the expiration date is 6 months; the production date and expiration date are shown in the outer packaging box.
2. Avoid repeated freezing and thawing of the kit and the number of freezing and thawing shall not exceed 7 times.
3. After opening, the bottles should be stored at -20 and protected from light. The number of bottles opening times should not exceed 7 times, which will not affect the use within the validity period.
[Applicable Instruments]
1. This kit has been validated on ABI7500 quantitative fluorescence PCR instrument.
2. For other models not listed, relevant experiments have not been performed or completed for this kit. If users need to use this type of instrument platform to carry out the detection of this reagent, please contact our Technical Department at for relevant support.
NB: The other devices can include quantitative fluorescence PCR platforms with FAM, VIC, ROX and Cy5 channels.
[Sample Requirements]
1. Nasopharyngeal swabs, oropharyngeal swabs and other methods are used to obtain samples, and it is recommended to use commercial virus sampling kits for sample collection devices.
[Test Results Interpretation]
1. Negative and positive controls should be tested in each experiment and the test result can be determined only when the controls meet the quality control requirements.
2. When FAM, VIC and ROX channels are positive, Cy5 channel result may be negative due to the system competition.
3. When the internal standard result is negative, if the FAM, VIC and ROX signals of the test sample are also negative, the test result of the sample is invalid, and the cause should be found and eliminated, and the experiment repeated for this sample.
[Product Performance Index]
1. Precision: The coefficient of variation Intra-batch / Inter-batch, Intra-day / Inter-day among different operators shall not be higher than 5.0%.
2. Coincidence rate of negative positive controls: The coincidence rate of positive controls and negative controls is 100%.
3. Minimum detection limit: The minimum detection limit of this kit is 500 copies/mL.
One Step Test for Novel Coronavirus (2019-nCoV) IgM/IgG antibody (Colloidal Gold) is intended for the qualitative detection of 2019-Novel Coronavirus IgM and IgG antibody in serum, plasma or whole blood samples from patients suspected of COVID-19 infection by a healthcare provider.
A kit contains:
Package specifications: 25 tests/box
1) Getein Novel Coronavirus (2019-nCoV) IgM/IgG antibody test card in a sealed pouch with desiccant
2) Sample diluent: 2 bottles/box
3) User manual: 1 piece/box
We are manufacturer and supplier of high quality molecular diagnostics product among covid 19 detection kits consisting of:
1]. covid 19/sars cov 2 nucleic acid test kits to detect the covid 19 standard, uk and south africa variants (rt pcr).
2]. covid 19/sars cov 2 antigen rapid test kits.
3]. covid 19/sars cov 2 antibody (igg/igm) rapid test kits.
in addition to a product of quality, we offer very competitive price and we have high production capacities to assure a continuous supply of product without shortage..Manufacture, oem
INTENDED USE
For qualitative detection of the nucleocapsid protein antigen of SARS-CoV-2 in nasopharyngeal and nasal swab, and saliva specimens from individuals and is aid in rapid diagnosis of patients with suspected SARS-CoV-2 infection.
FEATURES
Carefully selected special monoclonal antibody to the nucleocapsid protein antigen from SARS-CoV-2.
Various applicable specimen: Nasopharyngeal swab, Nasal swab and Saliva.
Easy to use, easy results interpretation by naked eyes.
Test result available within 15minutes.
TEST PROCEDURE: Very simple as per the instructions stated on the manual inserted in the kit.
RESULTS INTERPRETATION
Positive: A red line appears on the test line (T) and the control line (C).
NOTE: A positive result does not rule out co-infections with other pathogens.
Negative: Only the control line (C) appears, and no red line appears on the test line (T).
NOTE: A negative result does not exclude infection.
Invalid: There is no red line at the position of the control line (C). Regardless of whether the TEST line (T) is displayed, it is an invalid result and the sample should be tested again.
- LoD: 1.5�??102 TCID50 for virus lysate, 10pg/mL for recombinant Nucleocapsid protein antigen.
- Compared with NAT method, the specimens with the Ct range between 30-35 will be detectable.
- No cross-reactions with various bacteria, viruses and fungi normally available in respiratory track.
- Positive Agreement (95% CI): 97/100, 97% (83.3% - 99.9%)
- Negative Agreement (95% CI): 100/100, 100.0% (95.5% - 100%).
[Product Name]: SARS-CoV-2 Antigen Test
[Product Code]: Cat# FP-318
[Sample Type]: Nasopharyngeal swab / Nasal swab /Saliva
[Detection Method]: Colloidal Gold
[Reaction Time]: Within 15min
[Packing Size]: 1T x 20 cassettes + Sample buffer 20 vials x 0.5mL + 20 samples collection swab x 1.
[Storage Conditions]: 2*C ~ 30*C
[Shelf Life]: 12 months
[CE Mark Registration No.]: RPS/99/2021.
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Product description
120KV 10ma DC Cable Test System is an important equipment for DC voltage withstand test and leakage current test of HV electrical equipments, cables, surge arresters in electriv industry and power supply departments. 120KV 10ma DC Cable Test System is developed based on the calibration made by National HV Meterage Station, it accords with the standard "Generation Requirement of Portable HVDC Generator"(ZGF 24003-90)
The test transformer calls the booster, it is the basic test equipment used by the power station, supplying and distributing the electrical power system and the scientific research unit. Which used in the insulated intension test on all kinds of electrical products, electrical equipments and insulated materials, testing the insulated level of products, discovering the insulated objection of quizzee, scaling the capacity burdened voltage
INTENDED USE
For qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in serum, plasma (EDTA, sodium citrate and lithium heparin) or fingerstick whole blood, venous whole blood specimens from patients suspected of COVID-19 infection.
FEATURES
Coated with carefully selected specific Nucleocapsid and Spike protein antigen.
Detection for IgM and IgG antibodies simultaneously.
Simple operation, easy result interpreted.
Rapid test within 15 minutes.
RESULTS INTERPRETATION
Positive:
1. The presence of 3 red lines (T1, T2 and C) within the reaction window, no matter which band appears first, indicates presence of both SARS-CoV-2 IgM and IgG antibodies.
2. The presence of 2 red lines (T1 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgM antibody.
3. The presence of 2 red lines (T2 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgG antibody.
Negative:
1. The presence of line (control line) only within the reaction window indicates that no SARS-CoV-2 antibodies are detected. The results is negative.
Invalid:
1. If the control(C) line is not displayed in 10-15 min, regardless of whether T1 and/or T2 line is present, the test result is invalid. It is recommended that the specimen should be re-tested.
2. The test result is invalid after 15 min.
1. 5 LED digitally display output by actual value or by percentage
2. AC/DC current output range: 0~100 uA ~500uA ~2mA~5mA~20mA ~50mA ~200mA ~500mA ~2A~5A~20A~30A(optional)~50A(optional)
3. AC/DC voltage output range: 0~200mV~1V~2V~5V~10V~20V~50V~100V~200V~500V~1000V
4. Three AC frequency for option: 50Hz 60 Hz 400 Hz
5. Auto protection or manual resetting function for over load
6. Over load rang is 10% for each level of voltage current
7. Clip-on transformer testing: matching with our product of standard coil measuring range AC 0~750A ( above 1000A for part of meters) DC 0~1000A error: ±0.3%
TKDL-II live cable identification instrument is used to identify A particular cable in the power cable setting migration maintenance and fault treatment to identify A cable in the cable. It has the characteristics of accurate fast simple operation and wide application. It is an indispensable testing instrument in cable construction and maintenance. The electric/uncharged cable recognition device USES single-chip microcomputer technology to encode and power the transmitting signal at the transmitting end which drives the large calibre calipers to coupling the signal to the live cable. The single chip in the receiver decodes and phase the received phase encoding signal. The target cable is identified from a large bundle of other cables based on the uniqueness of the signal phase characteristics on the target cable. It is a light compact compact lithium battery powered portable instrument. Suitable for all kinds of high and low voltage power cables.
1. Charged identification and un-charged identification function combined not only for identification and judgment of cable outage but also for the identification and judgment of live cables the operation is extremely simple very easy to use.
2. The instrument lithium battery-powered you can work continuously for 3 to 5 hours suitable for field use of passive field.
Measurement accuracy reaches medical grade
Test speed is 30s
Weak signal test (cufflink simulator test) is 20%
Blood pressure measuring range 40 ~ 255mmhg
Pulse rate 30bpm-~ 240bpm
Resistantof occasional interference movement, support serial, support the hibernation feature
Provide three¡¡éand five lead system with arrhythmia analysis function
Adopting digital filter technology
Selectable 50hz or 60hz band stop filter
500hz 7/12 lead synchronous sample and anylsis
Character classification up to tweel sort, and 3 channel st segment monitoring
Advanced dsp algorithm monishes the influence of motion artifact
All digital-signal processing improves accuracy of low perfusion
Small size easy to be assem ble
A wealth of experience in r&d, with perfect quality in the measurement precision
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