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42-49 of 49 products

  • S3004E UU – Ureaplasma Urealyticum DNA Fluorescence Diagnostic Kit

    Brief

    The Ureaplasma Urealyticum (UU) DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is used to detect the presence of UU-DNA in samples such as male urethra swab and female cervical swab. The detection result can be used as an aid in the diagnosis of a UU infection. The test provides a molecular diagnostics-based solution for early diagnosis of venereal disease and for preliminary screening of high-risk venereal disease groups.

    Parameters

    Product features Parameter
    Specimen Type Genital tract secretions.
    Technical Platform One-tube fast release technology Advanced magnetic beads technology
    Target pathogen UU
    Internal Control Recombinant plasmid
    PCR Instrument ABI7500,QuantStudio 5, Stratagene Mx3000P, MA-6000, SLAN-96P, LightCycler® 480 II,iPonatic S-Q31A&B,S-Q36A
    Amplification Time 70 min
    Sensitivity 400 copies/mL
    Spec. 48T, 12-P
    Qualification CE
  • S3003E NG – Neisseria Gonorrhoeae DNA Fluorescence Diagnostic Kit

    Brief

    Neisseria Gonorrhoeae (NG) DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is used to detect the presence of NG-DNA in samples such as male urethral swab and female cervical swab. The detection result can be used as an aid in the diagnosis of an NG infection. The test provides a molecular diagnostics-based solution for early diagnosis of venereal disease and for preliminary screening of high-risk venereal disease groups.

    Parameters

    Product features Parameter
    Specimen Type Genital tract secretions.
    Technical Platform One-tube fast release technology Advanced magnetic beads technology
    Target pathogen NG
    Internal Control Recombinant plasmid
    PCR Instrument ABI7500, QuantStudio 5, Stratagene Mx3000P, MA-6000, SLAN-96P, LightCycler® 480 II, iPonatic S-Q31A&B, S-Q36A
    Amplification Time 70 min
    Sensitivity 400 copies/mL
    Spec. 48T, 12-P
    Qualification CE
  • S3001E CT – Chlamydia Trachomatis DNA Fluorescence Diagnostic Kit

    Brief

    Chlamydia Trachomatis (CT) DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) applies to detect CT DNA in specimens like reproductive tract secretion. The detection result can be used for aiding diagnosis of CT infection, which provides molecular diagnosis base for early diagnosis of venereal disease and for preliminary screening of venereal disease high-risk groups.

    Parameters

    Product features Parameter
    Specimen Type genital tract secretions.
    Technical Platform One-tube fast release technology Advanced magnetic beads technology
    Target pathogen CT
    Internal Control Recombinant plasmid
    PCR Instrument ABI 7500, Roche LC480,Stratagene Mx3000P
    Amplification Time 70 min
    Sensitivity 400 copies/mL
    Spec. 48T
    Qualification CE
  • S3050E CT/UU/NG – Chlamydia Trachomatis/Ureaplasma Urealyticum/Neisseria Gonorrhoeae DNA Diagnostic Kit

    Brief

    Chlamydia Trachomatis/Ureaplasma Urealyticum/Neisseria Gonorrhoeae DNA Diagnostic Kit (PCR-Fluorescence Probing) is a qualitative in vitro test for simultaneous detection of Chlamydia Trachomatis, Ureaplasma Urealyticum and Neisseria Gonorrhoeae DNA in sterile calcium alginate swab specimens from male urinary tract secretion and female genital tract secretion by applying real-time fluorescence quantitative PCR technique, which can provide molecular diagnosis evidence for the early diagnosis of related sexually transmitted diseases and initial screening of high-risk STD population.

    Parameters

    Product features Parameters
    Specimen Type genital tract secretions.
    Technical Platform One-tube fast release technology Advanced magnetic beads technology
    Target pathogen CT, UU, NG-DNA
    Internal Control β--globin gene
    PCR Instruments ABI7500,SLAN-96P
    Amplification Time 70 min
    Sensitivity 400 copies/mL
    Spec. 48T
    Qualification CE
  • S3113E SC2/FluA/B – SARS-CoV-2 and Influenza A/B Virus Nucleic Acid Diagnostic Kit

    Brief

    Most people infected with the COVID-19 virus will experience mild to moderate respiratory illness and recover without requiring special treatment. Elder people, and those with underlying medical problems like cardiovascular disease, diabetes, chronic respiratory disease, and cancer are more likely to develop serious illness.   Sansure COVID-19 diagnostic solutions are used to directly detect  the presence of viral RNA, which will be detectable in patients before antibodies form or symptoms of the disease are present, which means the test results can tell whether or not that someone gets virus very early on in their illness. This kit can also joint-detect RNA of influenza A virus and influenza B virus.

    Parameters

    Product features Parameters
    Specimen Type Oropharyngeal swab, sputum
    Extraction Platform One-tube fast release technology Advanced magnetic beads technology
    Target Genes SARS-CoV-2:ORF 1ab, N gene; influenza A:M gene; influenza B:NP gene
    Internal Control Rnase P gene
    PCR Instrument ABI7500, SLAN-96P, MA-6000, QuantGene 9600, iPonatic S-Q31A&B,S-Q36A
    Sensitivity 200 copies/mL
    Spec. 24T, 48T, 24-P
    Qualification CE
  • S3148E SC2/Flu/RSV – SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple Nucleic Acid Diagnostic Kit

    Brief

    The SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time RT-PCR test intended for the qualitative Diagnostic of nucleic acid from SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple in the nasopharyngeal swabs and oropharyngeal swabs from individuals.

     

    As the seventh coronavirus that infects humans, the SARS-CoV-2 can cause fever, fatigue, dry cough, dyspnea and other symptoms. In severe cases, it can cause acute respiratory distress syndrome, septic shock, and even death. At the same time, the SARS-CoV-2 has a strong spreading ability and has a wide range. Influenza virus (Influenza virus) can cause acute respiratory infections, with clinical manifestations of fever, headache, myalgia, fatigue, rhinitis, sore throat and cough. Influenza viruses can aggravate underlying diseases (such as heart and lung diseases) or cause secondary bacterial pneumonia or primary influenza viral pneumonia. The elderly and people with various chronic diseases or physical weakness are prone to severe complications and mortality higher after infecting influenza. Respiratory syncytial virus (RSV) belongs to the Pneumovirus genus of the Paramyxoviridae family. It mainly causes lower respiratory tract infections such as bronchiolitis and pneumonia in infants under 6 months, as well as rhinitis , Cold and other upper respiratory tract infections in older children and adults.

    Parameters

    Product features Parameter
    Covering pathogens
    SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus
    Specimen Types
    Nasopharyngeal swab and oropharyngeal swab
    Technical Platform
    One-tube fast release technology
    Advanced magnetic beads technology
    Internal Control
    RNase P gene
    Compatible Instrument
    ABI 7500; MA-6000; SLAN®-96P; iPonatic S-Q31A/S-Q31B/S-Q36A
    Sensitivity
    500 copies/mL.
    Qualification
    CE
  • S3102E SC2 – Novel Coronavirus (2019-nCoV) Nucleic Acid Diagnostic Kit

    Brief

    COVID-19 is an infectious disease caused by a newly discovered coronavirus named SARS-CoV2.   Most people infected with the COVID-19 virus will experience mild to moderate respiratory illness and recover without requiring special treatment. Elder people, and those with underlying medical problems like cardiovascular disease, diabetes, chronic respiratory disease, and cancer are more likely to develop serious illness.   Sansure COVID-19 diagnostic solutions are used to directly detect  the presence of viral RNA, which will be detectable in patients before antibodies form or symptoms of the disease are present, which means the test results can tell whether or not that someone gets virus very early on in their illness.

    Performance

    • One-tube/fast release technology
    • Up to 96 samples at one time
    • Simple operation process, less specialist training
    • Room temperature lysis, less contamination
    • Sampling types : nasopharyngeal swab, oropharyngeal swab, alveolar lavage fluid, sputum, serum, whole blood ,Feces
    • Enhance large-scale screening efficiency
    • Internal control: human housekeeping gene RNase P

    Parameters

    Product features Parameters
    Specimen Type Nasopharyngeal swab, oropharyngeal swab, alveolar lavage fluid, sputum, serum, whole blood, feces
    Extraction Platform One-tube fast release technology Advanced magnetic beads technology
    Internal Control Rnase P gene
    PCR Instrument ABI7500, QuantStudioTM 5, SLAN-96P, MA-6000, Bio-Rad CFX-96, QuantGene 9600, LightCycler 480, iPonatic S-Q31A&B,S-Q36A
    Sensitivity 200 copies/mL
    Spec. 24T, 48T, 24-P
    Qualification CE
  • S3121E SARS-CoV-2/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay)

    Brief

    SARS-CoV-2/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay) is intended for the qualitative detection of the SARS-CoV-2/InFluA/InFluB nucleocapsid protein in human nasopharyngeal or oropharyngeal swabs. Test results will be available for reading in 15-20 minutes. Positive results indicate the presence of viral antigens. This kit is for in vitro diagnostic use.

    Features

    • Accurate LOD 80TCID50 /ml, Specificity 100%
    • Convenient No instrument needed, easy to operate
    • Fast Result available in only 15-20 min

    Instruction

    Result interpretation

    Parameters

    Qualification CE

    Kit components

    No. Product Name Spec.
    S3121E-25
    SARS-CoV-2/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay)
    25 Test

    The kit components:

    • SARS-CoV-2/InFluA/InFluB Antigen Test Cassette (individually in a foil pouch with desiccant)
    • Sample Extraction Buffer
    • Swab
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