Shenzhen Kisshealth Biotechnology Co., Ltd

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SARS-CoV-2 RT PCR Test Kits Nucleic Acid Throat Swab Sample Fluorescence

China SARS-CoV-2 RT PCR Test Kits Nucleic Acid Throat Swab Sample Fluorescence

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SARS-CoV-2 RT PCR Test Kits Nucleic Acid Throat Swab Sample Fluorescence

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Payment Terms	T/T
Supply Ability	10,000,000 tests per day
Delivery Time	Within 5 days
Packaging Details	32 tests/kit, 48 tests/kit, 96 tests/kit
Product namee	SARS-CoV-2 Nucleic Acid Detection Kit (RT-PCR)
Application	Qualitative detection of COVID-19 nucleic acid test in throat swab or nasopharyngeal swab samples.
Principle	RT-PCR
Specimen	Throat swab or nasopharyngeal swab samples
Advantage	Results in 90 minutes
Model	K901-32T, K901-48T, K901-96T
Brand Name	KISSH
Model Number	K901-32T, K901-48T, K901-96T
Certification	CE
Place of Origin	CHINA

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Product Details
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Product Specification


Payment Terms	T/T	Supply Ability	10,000,000 tests per day
Delivery Time	Within 5 days	Packaging Details	32 tests/kit, 48 tests/kit, 96 tests/kit
Product namee	SARS-CoV-2 Nucleic Acid Detection Kit (RT-PCR)	Application	Qualitative detection of COVID-19 nucleic acid test in throat swab or nasopharyngeal swab samples.
Principle	RT-PCR	Specimen	Throat swab or nasopharyngeal swab samples
Advantage	Results in 90 minutes	Model	K901-32T, K901-48T, K901-96T
Brand Name	KISSH	Model Number	K901-32T, K901-48T, K901-96T
Certification	CE	Place of Origin	CHINA
High Light	SARS-CoV-2 PCR Test Kits ，Nucleic Acid PCR Test Kits ，Fluorescence Channels Nucleic Acid Test Kit

SARS-CoV-2 Nucleic Acid Detection Kit (RT-PCR)

【Test Principle】

This kit based on real-time PCR fluorescence technology, and the specific primers and corresponding fluorescent probes target to the conserved region of COVID-19 genome was designed for highly specific detection. By detecting the fluorescent signals changes, the COVID-19 nucleic acid from a throat swab or nasopharyngeal secretion specimen can be qualitatively detected.

【Sample Requirement】

1. Applicable sample type: Throat swab (Oropharyngeal swab/Nasal swab)

2. Sample collection

2.1 Sample time: The reagent is not affected by the specific clinical symptoms of patients, and

can be sampled at each stage of the course of the disease.

2.2 The test performance of the reagent is not affected when using the drugs described in the

analysis performance evaluation, and the sample can be taken normally. It is better to take

samples before using other unverified drugs

2.3 Throat swab requirement: It’s better to use long handle swab with polypropylene fiber head

or wood handle swab, please select the preservation solution suitable for cells and viruses.

It is better to directly select the commercial throat swab sampling tube.

3. Sampling method:

3.1 Oropharyngeal swab: Wipe both tonsils and the posterior pharyngeal wall with a swab with

moderate force to avoid touching the tongue.

3.2 Nasal swab: Use the swab to penetrate the nasal cavity for 2-3 cm, and rotate it for 2-3 times.

【Storage conditions and the period of Validity】

This kit shall be stored at the temperature below -20℃ in dark and avoid repeated freezing and

thawing (if freezing and thawing, must not exceed 4 times), with a validity period of 12 months. It

can be stored at -20℃ after opening the cover, with a validity period of 30 days. The kit shall be

transported in an ice box filled with 50% of the total volume of dry ice for no more than 5 days.

【Result judgment】

1. Determine the validity of the experiment:

The positive control FAM, VIC channel should have a typical amplification curve, and the Ct value is generally less than 36, but may

fluctuate due to different threshold settings of different instruments.

The negative control FAM, VIC channel should be non-amplified Ct. It is agreed that the above requirements must be met at the same time, otherwise this test is invalid.

2. Result judgment

FAM/VIC channel

Judgment result

Ct＜37

Sample test is positive

37≤Ct＜40

The amplification curve is S-shaped, and suspicious samples

need to be re-examined; if the re-examination results are

consistent, it is judged as positive, otherwise it is negative.

Ct≥40 Or No Amplification

Sample test is negative (or below the lower limit of kit detection)

Company Details

Bronze Gleitlager

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Business Type:

Manufacturer 
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Year Established:

2018 
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Total Annual:

10,000,000-30,000,000
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Employee Number:

50~150 
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Ecer Certification：

Active Member 

Shenzhen Kisshealh Biotechnology Co., Ltd., located in the Pingshan District, Shenzhen, P.R. China. is a diagnostics company focused on the development and manufacture of IVD tests at the Point-of-Care with highly innovative proprietary technology. We focused on the emerging markets of ... Shenzhen Kisshealh Biotechnology Co., Ltd., located in the Pingshan District, Shenzhen, P.R. China. is a diagnostics company focused on the development and manufacture of IVD tests at the Point-of-Care with highly innovative proprietary technology. We focused on the emerging markets of ...

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Shenzhen Kisshealth Biotechnology Co., Ltd
301,Building B1,Compass Life Science Industrial Park, Julongshan Road A, Pingshan District, Shenzhen,China
https://www.antigen-testkit.com/

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