GOLD STANDARD for diagnosis novel coronavirus. This kit is based on one-step RT-PCR technique. Used for the in vitro qualitative detection of novel coronavirus (2019-nCoV) ORF1ab and N gene in the throat swabs, sputum specimens of suspected pneumonia patients infected by novel coronavirus, suspected clustering cases and others needing diagnosis or differential diagnosis for novel coronavirus. No cross-reaction, sensitivity is 500 copies/ml. CFDA/CE. Applicable Instruments include ABI 7500 & LightCycler480.

ContactMOQ: 1 Unit

Daozhou Health Management Co., Ltd⚓ Harbor★4.5(0)

Supplier

Daozhou Health Management Co., Ltd

⚓ Harbor

★4.5(0)

⚡ <4h✓ 0.00%

⚓ Harbor

2019-nCOV Nucleic Acid Typing Test Kit

[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. [CE Mark Registration No.]: RPS/499/2021. [EC REP.]: CMC MEDICAL DEVICES & DRUGS S.L. C/ Horacio Lengo n18, C.P 29006, Milaga, Spain.

ContactMOQ: 1 Unit

Wuhan Healthcare Biotechnology Co., Ltd.⚓ Harbor★4.5(0)

Supplier

Wuhan Healthcare Biotechnology Co., Ltd.

⚓ Harbor

★4.5(0)

⚡ <4h✓ 0.00%

About Nucleic Acid Test Kit Trade

Nucleic Acid Test Kit is one of the most actively traded commodities in global B2B markets. Major exporting countries include Ukraine, Russia, Argentina, and India, which together account for over 80% of global production. Buyers from the Middle East, Africa, and Southeast Asia represent the largest import demand.

When sourcing Nucleic Acid Test Kit, buyers typically evaluate suppliers based on price per metric ton, minimum order quantities, certifications (ISO, HALAL, SGS), and payment terms. The most common payment methods used in nucleic acid test kit trade are Letter of Credit (L/C) and Telegraphic Transfer (T/T).

EximNext connects buyers with 1,240+ verified nucleic acid test kit suppliers across 67 countries. Post a buy requirement to receive competing quotes within 24 hours, or browse our verified supplier directory to compare prices, certifications, and response times.

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Nucleic Acid Test Kit — Suppliers, Manufacturers & Wholesale Exporters

2 Nucleic Acid Test Kit products from verified suppliers & exporters on EximNext B2B Marketplace

Covid-19 Nucleic Acid Test Kit (rt-pcr)

Supplier: Daozhou Health Management Co., Ltd, China

2019-nCOV Nucleic Acid Typing Test Kit

Supplier: Wuhan Healthcare Biotechnology Co., Ltd., China

Browse more products on EximNext B2B Marketplace — the leading import export marketplace for wholesale trade.