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DG-CV0201

Dow QuickFinder™-G 2019-nCoV Real-Time PCR Kit

  • Payment
    COD , O/A , T/T , WK
  • MOQ
    10,000 ea
  • Supply Ability
    1,000,000 ea per One-Time
  • Supply Details
    Sample Order

    Quantity Adjustable

  • Country of sale
    Asia, Americas, World Wide, Europe, Middle East
  • PRICE
    • FOB

      USD 5.00 ~ 6.00

      (1 ea)

ITEM SPECIFICS

  • Brand
    DG-CV0201
    Model Dow QuickFinder™-G 2019-nCoV Real-Time PCR Kit
  • origin
    Republic of Korea
  • Size(Capacity)
    105 x 52 x 62 (mm)
  • Weight
    50g
  • Function
    Used to measure the corona virus in phlegm, laryngeal and non-puric bacteria.
  • Features
    Real-time RT-PCR test at SARS-CoV-2 from patients suspected of COVID-19.
  • Expiry Date
    6 months
  • Condition
    Brand new
Dow QuickFinder™-G 2019-nCoV Real-Time PCR Kit
[Intended Use]
Dow QuickFinder™-G 2019-nCoV Real-Time PCR assay is a real-time RT-PCR assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal or oropharyngeal swab specimens from patients suspected of COVID-19 by their healthcare provider.

The SARS-CoV-2 is generally detectable in nasopharyngeal and oropharyngeal swab specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 genetic material. Clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out co-infection with other pathogens. Laboratories with in the United States and its territories are required to report all positive results to the appropriate public health authorities (local, state and federal).

Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.

Dow QuickFinder™-G 2019-nCoV Real-Time PCR assay is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time polymerase chain reaction (PCR) and in vitro diagnostic procedures.
[Summary]
An outbreak of pneumonia of unknown etiology in Wuhan City, Hubei Province, China was initially reported to the World Health Organization (WHO) in December 2019. Chinese authorities identified a novel coronavirus SARS-CoV-2 (previously called 2019-nCoV) which has resulted in confirmed human infections worldwide, including the United States.

Cases of asymptomatic infection, mild to severe respiratory illness, as well as deaths, have been reported. Patients can become infected with the SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person).

Dow QuickFinder™-G 2019-nCoV Real-Time PCR assay is a molecular in vitro diagnostic test for the detection of the SARS-CoV-2 RNA in nasopharyngeal or oropharyngeal swab specimens from patients suspected of COVID-19 by their healthcare provider and aids the diagnosis of coronavirus disease 2019. The assay is based on a widely used ribonucleic acid amplification methodology.
[Principles of the Test]
In Dow QuickFinder™-G 2019-nCoV Real-Time PCR assay kit 3 (three) sets of the oligonucleotide primers and probes for detection of SARS-nCoV-2 were selected from regions of the viral nucleocapsid (N) gene. The following regions are detected by Dow QuickFinder™-G 2019-nCoV Real-Time PCR assay:
• N1
• N2
• N3

RNA isolated and purified from upper and lower respiratory specimens is reverse transcribed to complementary DNA (cDNA) and subsequently amplified in Real-Time PCR Instrument. In the process, the probe anneals to a specific target sequence located between the forward and reverse primers. During the extension phase of the PCR cycle, Taq polymerase degrades the probe by its 5' exonuclease activity, causing the reporter dye to separate from the quencher dye, generating a fluorescent signal. With each cycle, additional reporter dye molecules are cleaved from their respective probes, increasing the fluorescence intensity. Fluorescence intensity is monitored at each PCR cycle by the Applied Biosystems® 7500 Real-Time PCR System.

Detection of SARS-nCoV-2 RNA not only aids in the diagnosis of COVID-19 but also provides epidemiological and surveillance information.
Materials Required (Provided)
Reagent Label Description Volume (uL per vial)
(50 test)
Volume (uL per vial)
(100 test)
Storage conditions
Dow QuickFinder-G-PM1 Set of primers and probes specific
to RdPp gene and HS-Rp30 gene
125 250 -20°C (protect from light)
Dow QuickFinder-G-PM2 Set of primers and probes specific
to RdPp gene and HS-Rp30 gene
125 250 -20°C (protect from light)
Dow QuickFinder-G-CV3 Set of primers and probes specific
to N gene sequence 1 and HS-Rp30 gene
125 250 -20°C (protect from light)
Dow QuickFinder-G-PM4 Set of primers and probes specific
to N gene sequence 2 and HS-Rp30 gene
125 250 -20°C (protect from light)
Dow QuickFinder-2019-nCoV Master Mix Master Mix 1,000 1,000 x 2 -20°C (protect from light)
Dow QuickFinder-G PM 1 Control 2019-nCoV N gene and Set of primers and
probes specifiec human RNAse P
50 100 -20°C (protect from light)
Dow QuickFinder-G PM 2 Control 2019-nCoV N gene and Set of primers and
probes specifiec human RNAse P
50 100 -20°C (protect from light)
Dow QuickFinder-G PM3,PM4 Control 2019-nCoV N gene and Set of primers and
probes specifiec human RNAse P
50 100 -20°C (protect from light)
 
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R&D CERTIFICATE

  • ISO13485 
    IAF 
    02.04.2020 
    인증서보기
  • EC Declaration of Conformity 
    KTR Europe GmbH 
    29.04.2020 
    인증서보기
  • 2017 Hi Seoul Good Products Award 
    Seoul Business Agency 
    2017.12.7 
    인증서보기
  • Korea International Women's Invention Exposition 
    Korean Women Inventors Association 
    2019.6.23 
    인증서보기

PAYMENTS DETAILS

This supplier supports payments for offline orders
  • Open Account : O/A
  • Cash On Delivery : COD
  • WK
  • Telegraphic Transfer : T/T
Contact Payment Manager
  • Name : Hwang Choon Hong
  • Tel : 82-0261166400
  • Email : dowgene@hanmail.net

SHIPPING

Shipping from : Republic of Korea
  • 233 Gasan digital 1-ro, Geumcheon-gu, Seoul (08501)
DowGene DNA Testing Company Co., Ltd.

DowGene DNA Testing Company Co., Ltd.

www.dowgene.com Seller_Mail
  • The person in charge

    Choon Hong Hwang
  • Telephone

    82-261166400
  • Fax

    82-261166404
  • Address

    233 Gasan digital 1-ro, Geumcheon-gu, Seoul (08501)

(주)다우진유전자연

DowGene DNA Testing Company Co., Ltd.
Introduction
DowGene DNA Testing Company Co., Ltd. develops and provides DNA-related services and products, and our services and products include DNA profile tests for paternity verification, kinship verification, individual identification, remains identification, DNA profile tests for prevention of missing children, food foreign substance detection and kind identification tests, DNA analysis services and DNA storage cards. DowGene DNA Testing Company Co., Ltd. is a KOLAS internationally certified testing laboratory and has been Korea's leading DNA testing organization certified by the Ministry of Heath and Welfare-affiliated Korean Institute of Genetic Testing Evaluation as a Class A DNA testing institution since the year 2007. All tests performed by DowGene DNA Testing Company are carried out in accordance with a testing quality management system and the best research personnel composed of doctoral researchers who participate in the testing activities to provide the best test quality and accuracy. We promise that DowGene DNA Testing Company will be the foremost company in the DNA analysis field, which will lead the bio-technology industry, based on our unmatched DNA identification technologies and continual research and development activities.
  • Business Type :
    Manufacturer
  • Main Product :
    COVID19 kit
  • Established :
    2007-08-27

R&D CERTIFICATE

  • 2017 Hi Seoul Good Products Award 
    Seoul Business Agency 
    Dec 7 2017 
    인증서보기
  • Korea International Women's Invention Exposition 
    Korean Women Inventors Association 
    23 Jun 201 
    인증서보기
  • ISO13485 
    IAF 
    02.04.2020 
    인증서보기
  • EC Declaration of Conformity 
    KTR Europe GmbH 
    29.04.2020 
    인증서보기
  • 2017 Hi Seoul Good Products Award 
    Seoul Business Agency 
    2017.12.7 
    인증서보기
  • Korea International Women's Invention Exposition 
    Korean Women Inventors Association 
    2019.6.23 
    인증서보기

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