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LightCycler® 96 System

Country Specific Labeling See country-specific product labeling for regulatory status.
Product image for LightCycler® 96 System

Set your research apart, with maximized sensitivity and fast time-to-result.

The versatile, plate-based LightCycler® 96 System helps you achieve fast, highly sensitive, and reproducible results for qualitative and quantitative detection of nucleic acids and SNP analysis.

LightCycler 96
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Features and benefits

Compact and easy to use, the LightCycler® 96 System Primary is the ideal companion for applications including gene expression analysis, gene detection, mutation detection, methylation analysis, miRNA research, and relative quantification of target genes.

 

Have confidence in the data you generate and quickly get publication-ready results

 

  • Fast precision thermocycling and innovative glass fiber optics for unbiased 96-well data capture.
  • Accurate results expected from a LightCycler® System—now including gradient functions.
  • Robust multiplex gene expression and high-resolution melt (HRM) assays without the need for passive reference dyes or temperature calibration.

 

Work economically, flexibly adapting your workflow to your assay format and throughput needs
 
  • Cost-effective value packs of optimized reagents and disposables.
  • Choose between multiwell plates and clear or white tube strips provided with caps.
  • Avoid unnecessary waiting time during preheating by starting experiments in standby mode.

 

Speed time to results with advanced yet easy-to-use software designed for both novice and experienced users
 
  • Benefit from a large, intuitive touchscreen interface and powerful data analysis.
  • Choose your type of connectivity via network or USB stick.
  • Create pdf or HTML reports from your data directly on the instrument.

Regulatory disclaimer

For life science research only. Not for use in diagnostic procedures.

Package inserts

Access package inserts through your country’s Roche Diagnostics Website.

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    Overview

    Ordering Information

    Technical Documents

    Access important product documentation including relevant certificates and other resources.

    After clicking below, you will be redirected to eLabDoc, where you can select your local country-specific documents.
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    Country Specific Labeling See country-specific product labeling for regulatory status.
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    IVD For in vitro diagnostic use.
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    cobas® eplex blood culture identification Gram-Negative panel
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    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> Babesia
    cobas® Babesia Nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> Babesia
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    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> SARS-CoV-2 &amp; Influenza A/B
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    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HIV-1/HIV-2 Qualitative
    cobas® HIV-1/HIV-2 Qualitative Nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> EBV
    cobas® EBV Quantitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    <b>cobas</b><sup>®</sup> SARS-CoV-2
    cobas® SARS-CoV-2 Nucleic acid test for use on the cobas® liat system Inform decisions at the POC with targeted RT-PCR SARS-CoV-2 test results in 20 minutes for both asymptomatic and symptomatic individuals using the cobas® liat system.
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    <b>cobas</b><sup>®</sup> HBV RNA
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    IVD For in vitro diagnostic use.
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    cobas® CT/NG Qualitative nucleic acid test for use on the cobas® 5800/6800/8800
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HSV 1 and 2 Test
    cobas® HSV 1 and 2 Test for use on the cobas® 4800 System
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> DNA Sample Preparation Kit
    cobas® DNA Sample Preparation Kit The cobas® DNA Sample Preparation Kit is used for manual sample preparation to isolate genomic DNA from formalin-fixed paraffin-embedded tumor tissue (FFPET) samples.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HCV
    cobas® HCV Quantitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HCV
    cobas® HCV Quantitative nucleic acid test for use on the cobas® 4800 System
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> TV/MG
    cobas® TV/MG Qualitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
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    IVD For in vitro diagnostic use.
    <b>cobas<sup>®</sup></b> MPXV
    cobas® MPXV Qualitative assay for use on the cobas® 6800/8800 Systems cobas® MPXV for use on the cobas® 6800/8800 Systems (cobas® MPXV) is a real-time PCR assay for the qualitative detection of DNA from Monkeypox virus (MPXV, clade I/II) in human lesion swab specimens (i.e., swabs of acute pustular or vesicular rash) from individuals suspected of monkeypox infection by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42.U.S.C. §263a, that meet requirements to perform moderate or high complexity tests.Results are for the identification of monkeypox virus (clade I/II) DNA, which is generally detectable in human pustular or vesicular lesion specimens during the acute phase of infection. Positive results are indicative of the presence of monkeypox virus (clade I/II) DNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results obtained with this device do not preclude monkeypox virus (clade I/II) infection and should not be used as the sole basis for treatment or other patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.Laboratories within the United States and its territories are required to report test results to the appropriate public health authorities. cobas® MPXV is intended for use by qualified clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and on the use of the cobas® 6800/8800 Systems.cobas® MPXV is only for use under the Food and Drug Administration’s Emergency Use Authorization.
    RUO For Research Use Only. Not for use in diagnostic procedures.
    <b>cobas</b><sup>®</sup> SARS-CoV-2 Variant Set 1
    cobas® SARS-CoV-2 Variant Set 1 Qualitative assay for use on the cobas® 6800/8800 Systems The cobas® SARS-CoV-2 Variant Set 1 for use on the cobas® 6800/8800 Systems is an automated, multiplex, real-time RT-PCR assay for the qualitative detection and differentiation of SARS-CoV-2 mutations E484K, N501Y and deletion HV-69/70 in e.g., nasal and nasopharyngeal swab specimens from patients with known SARS-CoV-2 infection to support the understanding of variant epidemiology for Population Health Management.The cobas® SARS-CoV-2 Variant Set 1 assay is intended for research use only and is not for use in diagnostic procedures.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> cfDNA Sample Preparation Kit
    cobas® cfDNA Sample Preparation Kit The cobas® cfDNA Sample Preparation Kit is used for manual sample preparation to isolate circulating cell-free DNA (cfDNA) from plasma samples.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> 4800 BRAF V600 Mutation Test
    cobas® 4800 BRAF V600 Mutation Test
    <b>cobas</b><sup>®</sup> SARS-CoV-2 Duo
    cobas® SARS-CoV-2 Duo Qualitative and quantitative assay for use on the cobas® 6800/8800 Systems
    RUO For Research Use Only. Not for use in diagnostic procedures.
    <b>cobas<sup>®</sup></b> HDV
    cobas® HDV Quantitative nucleic acid test for use on the cobas® 5800/6800/8800 systems cobas® HDV for use on the cobas® 5800/6800/8800 Systems (cobas® HDV) is an in vitro nucleic acid amplification test for both the detection and quantitation of hepatitis D virus (HDV) RNA in human EDTA plasma or serum. cobas® HDV is intended for research use only and is not for use in diagnostic procedures. cobas® HDV can be used to support scientific research to understand the potential use of this biomarker.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HCV GT
    cobas® HCV GT HCV genotyping test for use on the cobas® 4800 System cobas® HCV GT is an in vitro nucleic acid amplification test for the qualitative identification of Hepatitis C Virus (HCV) genotypes 1 to 6 and genotype 1 subtypes a and b in human EDTA plasma or serum from individuals with chronic HCV infection, using the cobas® 4800 system: the cobas® x 480 instrument for automated sample processing and the cobas® z 480 analyzer for automated amplification and detection. cobas® HCV GT is intended for use in selecting individuals with chronic HCV infection for antiviral therapy and in determining the duration of therapy regimens according to the antiviral therapy prescribing information.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> 4800 CT/NG v2.0
    cobas® 4800 CT/NG v2.0 The cobas® CT/NG v2.0 Test is an automated, in vitro nucleic acid amplification test for the qualitative detection of Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (NG) DNA in urogenital specimens. The Test utilizes the Polymerase Chain Reaction (PCR) for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae DNA in male and female urine, self-collected vaginal swab specimens (collected in a clinical setting) clinician-collected vaginal swab specimens, and endocervical swab specimens, all collected in cobas® PCR Media (Roche Molecular Systems, Inc.), and cervical specimens collected in PreservCyt® solution. This test is intended as an aid in the diagnosis of chlamydial and gonococcal disease in both symptomatic and asymptomatic individuals.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> Factor II and Factor V Test
    cobas® Factor II and Factor V Test
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> MTB-RIF/INH
    cobas® MTB-RIF/INH for use on the cobas® 5800/6800/8800 Systems cobas® MTB-RIF/INH for use on the cobas® 5800/6800/8800 Systems is an automated, qualitative in vitro diagnostic test, that utilizes real-time polymerase chain reaction (PCR), for the direct detection of rifampicin-resistance associated mutations of the rpoB gene, and isoniazid-resistance associated mutations in the katG and inhA genes, of Mycobacterium tuberculosis, from human respiratory specimens. The test is intended for use on raw sputum, and digested and decontaminated (N-acetyl-L-cysteine/ NaOH treated) sputum and bronchial alveolar lavage (BAL) samples, that tested positive for Mycobacterium tuberculosis complex (MTBC) by cobas® MTB. This test is intended for use in conjunction with culture and drug susceptibility testing, and as a reflex test together with cobas® MTB, as an aid in the diagnosis of infection with a multidrug resistant M. tuberculosis (MDR-TB).
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> MAI
    cobas® MAI for use on the cobas® 5800/6800/8800 Systems cobas® MAI for use on the cobas® 5800/6800/8800 Systems is an automated, qualitative in vitro diagnostic test, that utilizes real-time polymerase chain reaction (PCR), for the direct detection and differentiation of Mycobacterium avium and Mycobacterium intracellulare DNA in human respiratory specimens including raw sputum, and digested and decontaminated (N-acetyl-L-cysteine/NaOH [NALC-NaOH]-treated) sputum and bronchoalveolar lavage (BAL) samples. This test is intended for use in conjunction with mycobacterial culture as an aid in the diagnosis of pulmonary M. avium and M. intracellulare complex (MAC) infections.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> MTB
    cobas® MTB for use on the cobas® 5800/6800/8800 Systems cobas® MTB for use on the cobas® 5800/6800/8800 Systems is an automated, qualitative in vitro diagnostic test, that utilizes real-time polymerase chain reaction (PCR), for the direct detection of Mycobacterium tuberculosis complex (MTBC) DNA, in human respiratory specimens; including raw sputum, and digested and decontaminated (N-acetyl-L- cysteine/NaOH [NALC-NaOH]-treated) sputum and bronchoalveolar lavage (BAL) samples. This test is for use with specimens from patients who are suspected of Mycobacterium tuberculosis infection, and who are not taking antituberculosis therapy. This test is intended as an aid in the diagnosis of pulmonary tuberculosis, and in conjunction with other laboratory findings, as well as clinical signs and symptoms.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> Plasma Separation Card
    cobas® Plasma Separation Card The cobas® Plasma Separation Card is intended for the collection and stabilization of dried plasma from whole blood specimens, for subsequent in vitro diagnostic examination.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> MPX
    cobas® MPX Multiplex HIV, HCV & HBV nucleic acid test for use on the cobas® 6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> MPX
    cobas® MPX Multiplex HIV, HCV & HBV nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> Influenza A/B &amp; RSV UC
    cobas® Influenza A/B & RSV UC Qualitative nucleic acid test for use on the cobas® 6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas<sup>®</sup></b> TaqScreen MPX Test, version 2.0
    cobas® TaqScreen MPX Test, version 2.0
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> DPX
    cobas® DPX Duplex HAV & parvovirus B19 nucleic acid test for use on the cobas® 6800/8800 Systems The cobas® DPX test is an in vitro test for the direct quantitation of parvovirus B19 genotypes 1, 2, and 3 DNA and the direct qualitative detection of Hepatitis A virus (HAV) genotypes I, II, and III RNA in human plasma.This test is intended for use as an in-process test to quantify parvovirus B19 DNA alone or to simultaneously quantify parvovirus B19 DNA and detect HAV RNA in plasma intended for further manufacture collected from donors of whole blood, blood components, or plasma. Plasma from all donors or manufacturing pools may be tested as individual samples or in pools comprised of aliquots of individual samples.This test is not intended for use on samples of cord blood.This test is not intended for use as an aid in diagnosis for parvovirus B19 or HAV.
    IVD For in vitro diagnostic use.
    Roche Cell Collection Medium
    Roche Cell Collection Medium Roche Cell Collection Medium is designed for the preservation and transport of cells to be used in molecular testing and/or for the preparation of cytology slides.
    IVD For in vitro diagnostic use.
    <b>cobas<sup>®</sup></b> Respiratory flex
    cobas® Respiratory flex Qualitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> HEV
    cobas® HEV Nucleic acid test for use on the cobas® 5800/6800/8800 Systems The cobas® HEV test for use on cobas® 5800/6800/8800 Systems is a qualitative in vitro nucleic acid amplification test for the direct detection of hepatitis E virus (HEV) RNA (genotypes 1-4) in human plasma.This test is intended for use to screen donor samples for HEV RNA in plasma samples from individual human donors, including donors of whole blood, blood components (red cells, platelets, and plasma), and other living donors. Plasma from all donors may be screened as individual samples. For donations of whole blood and blood components, plasma samples may be tested individually or plasma may be tested in pools comprised of aliquots of individual samples.This test is not intended for use on samples of cord blood.This test is not intended for use as an aid in diagnosis for HEV.
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> BKV
    cobas® BKV Quantitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
    IVD For in vitro diagnostic use.
    symbol for cobas synergy software
    cobas® Synergy Software For use with cobas® 6800/8800 Systems, cobas® 5800 system, Microlab® STAR IVD, and Microlab® STARlet IVD High capacity pooling and archiving of blood donations
    IVD For in vitro diagnostic use.
    <b>cobas</b><sup>®</sup> CMV
    cobas® CMV Quantitative nucleic acid test for use on the cobas® 5800/6800/8800 Systems
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