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Covid-19 CLONIT SRL

Laboratorio clínico

COVID-19 Variant Detection Kit
COVID-19 Variant Catcher

The COVID-19 Variant Catcher is a qualitative test that allows for the identification, by means of Real Time PCR, of the S gene mutations HV 69-70del, E484K and N501Y for discrimination of SARS-CoV-2 (Wuhan strain) from SARS-CoV-2 strains B.1.1.7 (UK variant), B.1.351 (South African variant) and P.1 (Brazilian variant). The procedure allows for the detection of the RNA target by means of a reverse-amplification reaction in reaction tubes or microplate wells. The kit must be used with a RNA extracted from samples tested as positive for SARS-CoV-2 virus with the current validated methods on the market.

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COVID-19 Real Time PCR Test
COVID-19 HT Screen (RT-25HT)

The COVID-19 HT Screen (RT-25HT) is a qualitative test that allows for the identification, by means of Real Time PCR of the N region (nucleocapsid phosphoprotein) of SARS-CoV-2 in subjects with suspected COVID-19 infection. The procedure allows for the detection of the RNA target by means of a retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).

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FluA/FluB/SARS-CoV-2 Kit
FluA/FluB/SARS-CoV-2

The FluA/FluB/SARS-CoV-2 kit is a qualitative test that allows for the identification and discrimination, by means of Real Time PCR, of the Matrix gene (M1) for FluA, of the non structural gene 2 (NS2) for FluB and of the N region (nucleocapsid phosphoprotein) for SARS-CoV-2 (CoV2). The procedure allows for the detection of the RNA target by means of a one-step retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).

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COVID-19 Kit CE-IVD
quanty COVID-19v2

The quanty COVID-19 kit CE-IVD is a quantitative test that allows the quantification, by means of Real Time PCR of the N region (nucleocapsid phosphoprotein) of the novel Coronavirus (COVID-19). The procedure allows for the detection of the RNA target by means of a retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).

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Sobre CLONIT SRL

Clonit srl is a biotechnology company that develops innovative and reliable analytical methods in the field of In Vitro diagnostics using molecular biology techniques. The systems are useful for human diagnostic with particular attention to the detection of viral, bacteria and protozoa infections, genetic mutations and oncological diseases. The scientific innovations were transferred into ready to use diagnostic kits that, for the operating user-friendliness and the quality, are optimal for routine diagnostic laboratories.

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Cytomegalovirus Real-Time PCR Test
Quanty CMV Virus System

The Quanty CMV Virus System is an in vitro Real-Time PCR test developed for the identification and quantification of Cytomegalovirus (CMV) by targeting the IEA genomic region. Especially critical in post-transplantation monitoring, this assay enables early antiviral intervention by delivering reliable quantification. It operates on a Real-Time PCR analyser equipped with fluorescence detection and is suited for clinical laboratories managing immunocompromised patients.

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West Nile Virus Real-Time PCR Test
Quanty WNV System

The Quanty WNV System is a quantitative Real-Time PCR assay designed to amplify the 3’UTR region of West Nile Virus RNA, with specificity to differentiate it from the closely related Usutu virus. The test uses a one-step retro-amplification protocol and is run on a Real-Time PCR analyzer with integrated fluorescence detection. It supports precise quantification of WNV in diagnostic settings, especially in regions where flaviviruses co-circulate.

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Usutu Virus Real-Time PCR Test
Quanty Usutu System

The Quanty Usutu System is a Real-Time PCR-based quantitative assay that targets the 3’UTR region of Usutu virus RNA. It uses a one-step retro-amplification reaction for accurate quantification and is intended for use with a Real-Time PCR analyser featuring fluorescence detection. This system enables early and specific detection of Usutu virus, supporting diagnostic and surveillance workflows in areas at risk of flavivirus circulation.

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Laboratorio clínico

Cytomegalovirus Real-Time PCR Test
Quanty CMV Virus System

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West Nile Virus Real-Time PCR Test
Quanty WNV System

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Usutu Virus Real-Time PCR Test
Quanty Usutu System

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Malaria Real-Time PCR Test
Malaria Screening

Malaria Screening is a qualitative Real-Time PCR test designed to detect the DNA of Plasmodium species, including P. falciparum, P. malariae, P. vivax, P. ovale, and P. knowlesi from biological samples. The assay performs genomic amplification without species discrimination and requires a Real-Time PCR analyzer equipped with fluorescence detection and dedicated software. It is suitable for reliable malaria diagnosis where species-specific identification is not essential.

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Ureaplasma Urealyticum Test
Duplicα RealTime Ureaplasma Urealyticum Kit

The Duplicα RealTime Ureaplasma urealyticum Kit detects Ureaplasma urealyticum DNA via Real-Time PCR. This bacterium, part of normal genital flora, is associated with conditions like non-specific urethritis and premature birth. The kit targets the urease complex gene and provides accurate results for diagnosing infections linked to Ureaplasma.

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Chikungunya Virus Test
quanty Chikungunya System

The quanty Chikungunya System is a Real-Time PCR test for the detection and quantification of Chikungunya virus RNA in plasma or serum. It amplifies the nsP2 region, offering a reliable diagnostic tool for Chikungunya fever. The system ensures efficient, sensitive detection, essential for monitoring outbreaks in endemic areas.

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Leishmania Real-Time PCR Test
Leishmaniae spp. System

The Leishmaniae spp. System is a qualitative Real-Time PCR test designed to amplify the 18S ribosomal RNA gene of Leishmania species. Used for detecting Leishmania DNA in whole blood, this test supports timely and accurate diagnosis of Leishmaniasis. It ensures high sensitivity and specificity, critical for effective disease management.

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Zika Virus Test
quanty Zika System

The quanty Zika System is a quantitative Real-Time PCR test that amplifies the NS5 region of Zika Virus RNA. This system allows for the detection and quantification of Zika virus in serum, saliva, or urine samples. It provides a reliable method for diagnosing Zika virus infection, crucial for early detection in emerging regions.

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Dengue Virus Molecular Diagnostic Kit
Dengue Serotyping System

The Dengue Serotyping System is a state-of-the-art molecular diagnostic kit designed to accurately identify and differentiate the four serotypes of the Dengue virus. Utilizing advanced real-time PCR technology, this system delivers rapid and reliable results, making it an indispensable tool for clinical and research laboratories. Its high sensitivity and specificity ensure precise detection even in low-viral-load samples.

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CAG Repeat Expansion Kit
Huntington Disease Kit 1 – FL

The Huntington Disease Kit 1 – FL is an innovative molecular diagnostic tool designed to detect CAG trinucleotide repeat expansions in the HTT gene associated with Huntington’s disease. Utilizing advanced fluorescent PCR technology, this kit provides precise and rapid analysis, enabling early and accurate diagnosis. Its high sensitivity and specificity allow the detection of even small expansions, critical for clinical assessments.

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Y Chromosome Microdeletion Kit
Chromosome Y Microdeletion Kit

The Chromosome Y Microdeletion Kit is a cutting-edge diagnostic solution for detecting microdeletions in the AZF (azoospermia factor) regions of the Y chromosome, a key factor in male infertility. Utilizing advanced multiplex PCR technology, this kit provides rapid and accurate results, enabling precise identification of genetic abnormalities. It features high sensitivity and specificity, ensuring reliable detection even in challenging samples.

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HFE C282Y Mutation Detection Kit
Duplicα RealTime Mix & Match HFE C282Y Kit

The Duplicα RealTime Mix & Match HFE C282Y Kit is a cutting-edge diagnostic tool designed for precise, real-time detection of HFE C282Y mutations associated with hereditary hemochromatosis. Offering high sensitivity and accuracy, it allows for efficient genetic testing, facilitating personalized treatment plans and early intervention for patients at risk.

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Urine cfDNA Extraction Kit
CloNext Urine cfDNA Extraction Kit

The CloNext urine cfDNA extraction kit is designed for extracting circulating DNA from urine and applies unique magnetic beads technology. Used in combination with the CloNext series of automatic instruments, the kit achieves superior product quality, consistent and high product yield, and reproducible results.

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Blood DNA Kit
Clon Duplicα Blood DNA Kit

The Clon Duplicα blood DNA kit is intended for the isolation of nucleic acids from human whole blood samples for subsequent in vitro diagnostic purposes. The kit is based on proprietary magnetic beads technology and is to be used with the Duplicα PREP automatic extraction system.

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Nucleic Acid Extraction Kit
CloNext Viral Nucleic Acid Extraction Kit LV

The CloNext Viral Nucleic Acid Extraction kit LV is designed for extracting large volumes of viral nucleic acids from plasma, serum, or cell-free body fluids with sample volumes ranging up to 1000 µL and 2000 µL. The kit uses unique magnetic beads technology and in combination with the CloNext series of automatic instruments, achieves superior product quality, consistent and high product yield, and reproducible results.

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Automated Nucleic Acid Extractor
Duplica Prep 2

The Duplica Prep 2 is an automated nucleic acid extractor for the preanalytical preparation of samples for use with in vitro diagnostic clinical sample concentrating kits. It is based on the M-PVA Magnetic Bead proven technology for magnetic particle separation and delivers a high yield of pure DNA/RNA to ensure the success of downstream applications.

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STI Detection Kit
CT/NG Kit

The CT/NG Kit is an in vitro diagnostic test for the identification of Chlamydia trachomatis and Neisseria gonorrhoeae genomes by Real-Time PCR. The test targets the cystein-rich outer membrane protein genomic region and dnaB-like plasmidic gene of the Chlamydia trachomatis genome (including the Swedish variant) and the opa gene of Neisseria gonorrhoeae.

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Neisseria Gonorrhoeae Test
Duplicα RealTime Neisseria Gonorrhoeae 2nd Generation Detection Kit

The Duplicα RealTime Neisseria gonorrhoeae 2nd generation detection kit is an in vitro diagnostic test for the detection of Neisseria gonorrhoeae (NG) DNA by Real-Time PCR. The test targets cryptic plasmid pJD1 and 16S rRNA and is compatible with the most common Real-Time PCR systems.

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Clostridium Difficile A/B Test
Duplicα RealTime Advanced Clostridium Difficile A/B Kit

The Duplicα RealTime Advanced Clostridium Difficile A/B Kit is an in vitro diagnostic test for the detection of Clostridium difficile toxins A and B DNA by Real-Time PCR. The test requires stool samples and is compatible with the most common Real-Time PCR systems.

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Mucormycosis Real-Time PCR Kit
MucorGenius Multiplex Real-Time PCR Kit

The MucorGenius Multiplex Real-Time PCR Kit is intended for the direct detection of clinically relevant Mucorales species in BAL samples. It offers sample-to-result in less than three hours and is the only commercial real-time PCR kit available that aids in the diagnosis of mucormycosis.

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Malaria Test
Malaria Panel

The Malaria Panel is a qualitative test that allows the DNA amplification in Real-Time PCR, of P.falciparum, P.ovale, P.malariae and P.vivax genome extracted from biological samples. The procedure allows the detection of the DNA target (18s Ribosomal RNA gene) through a genomic amplification reaction and the identification of the four different species of Malaria P.falciparum, P.ovale, P.malariae, and P.vivax. The analysis of the results is obtained using a Real-Time PCR analyzer (thermal cycler integrated with a system for fluorescence detection and dedicated software)

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Hepatitis D Virus Test
quanty HDV System

The quanty HDV system is a molecular assay for the identification and quantification of the Hepatitis D genome, by one-step RT-PCR Real-Time. It uses plasma and serum diagnostic samples and runs on the Applied Biosystems 7500 Fast (ThermoFisher SCIENTIFIC) and Rotor-Gene Q MDx (RG-Q MDx - QIAGEN) Real-Time PCR instruments.

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Cardiovascular Disease GeneticTest
Duplicα RealTime Factor V R306T Cambridge Genotyping Kit

Duplicα RealTime Factor V R306T Cambridge Genotyping Kit is an in vitro diagnostic test for the detection of the allelic variant g.169524537C>G of the blood coagulation Factor V gene in human genomic DNA, by Real-Time PCR. It requires peripheral whole blood samples collected in EDTA and is compatible with the most common Real-Time PCR Systems.

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Male Infertility Test
RHYMA TEST IVF AZF STRIP TEST

The RHYMA TEST IVF AZF STRIP TEST is an in vitro diagnostic assay for the multiplex detection of the Sequence Tagged Sites (STSs) microdeletions into the AZF gene regions: AZFa region (sY84, sY86); AZFb region (sY127, sY134) and AZFc region (sY254 and sY255) in human DNA, by Reverse Hybridization Technology. The assay detects also the ZFX/ZFY gene (as internal control) and SRY gene (as additional control).

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Beta-Fibrinogen 455G>A Test
DuplicαRealTime Beta-Fibrinogen 455G>A Genotyping Kit

The DuplicαRealTime Beta-Fibrinogen 455G>A Genotyping Kit is an in vitro diagnostic test for the detection, by Real-Time PCR, of the allelic variant 455G>A in the promoter region of the Human Beta-Fibrinogen gene, in genomic DNA. It is compatible with the most common Real-Time PCR Systems as well as with the most common DNA extraction and purification systems.

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Tuberculosis Test
Duplicα RealTime Mycobacterium Tuberculosis Complex Kit

The Duplicα RealTime Mycobacterium tuberculosis Complex Kit is an in vitro diagnostic test for the detection of Mycobacterium tuberculosis complex (M.tuberculosis, M.africanum, M.bovis and M.microti), by Real-Time PCR. It is compatible with the most common Real-Time PCR Systems as well as with the most common DNA extraction and purification systems.

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Mycoplasma Hominis Test
Duplicα RealTime Mycoplasma Hominis Kit

The Duplicα RealTime Mycoplasma hominis Kit is an in vitro diagnostic test for the detection of Mycoplasma hominis (MH) DNA, by Real-Time PCR. It is compatible with the most common Real-Time PCR Systems as well as with the most common DNA extraction and purification systems.

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Toxoplasma Gondii Test
quanty Toxo

The quanty Toxo system is an in vitro diagnostic test for identification and quantification of the Toxoplasma gondii genome by Real-Time PCR. It uses diagnostic samples of whole blood collected in EDTA and amniotic fluid.

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Measles RT Real-Time PCR Test
quanty Measles

The quanty Measles system is an in vitro diagnostic test for identification and quantification of the N3 region of the Measles virus genome, by one-step RT- Real-Time PCR. It targets the N3 region of the measles virus genome and requires serum and urine diagnostic samples.

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Chlamydia Trachomatis Test
Chlamydia Trachomatis Kit

The Chlamydia trachomatis kit is an vitro diagnostic test for the identification Chlamydia trachomatis genome, by Real-Time PCR. It targets the cystein-rich outer membrane protein genomic region and dnaB-like plasmidic gene and requires diagnostic samples taken from vaginal swabs, cervical swabs, urethral swabs, and urine.

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Legionella Real-Time PCR Test
The Duplicα RealTime Legionella spp. Detection Kit

The Duplicα RealTime Legionella spp. Detection Kit is an in vitro diagnostic test for the detection of Legionella spp. DNA, by Real-Time PCR. It uses respiratory specimens as diagnostic samples and is compatible with commonly available DNA extraction and purification systems and Real-Time PCR systems.

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Genetic Cardiovascular Disease Test
Duplicα RealTime Mix & Match MTR A2756G Kit

The Duplicα RealTime Mix & Match MTR A2756G Kit is an in vitro diagnostic test for the detection, by Real-Time PCR, of the nucleotide substitution A2756G (allelic variant g.237048500A>G) of MTR gene in human genomic DNA. It requires peripheral whole blood samples collected in EDTA and is compatible with commonly available DNA extraction and purification systems and Real-Time PCR systems.

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Clostridium Difficile Test
Duplicα RealTime Advanced Clostridium Difficile A/B Kit

The Duplicα RealTime Advanced Clostridium Difficile A/B Kit is an in vitro diagnostic test for the detection of Clostridium difficile toxins A and B DNA, by Real-Time PCR. The test is compatible with the most common Real-Time PCR systems and DNA extraction and purification systems.

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Trichomonas Vaginalis Test
Duplicα RealTime Next Trichomonas Vaginalis Kit

The Duplicα RealTime Next Trichomonas vaginalis Kit is an in vitro diagnostic test for the detection of Trichomonas vaginalis (TV), by Real-Time PCR. The test is compatible with the most common Real-Time PCR systems and DNA extraction and purification systems.

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M.tuberculosis Real-Time PCR Test
Duplicα RealTime Mycobacterium Tuberculosis Complex Kit

Duplicα RealTime Mycobacterium tuberculosis Complex Kit is an in vitro diagnostic test for the detection of Mycobacterium tuberculosis complex (M.tuberculosis, M.africanum, M.bovis and M.microti), by Real-Time PCR. The test is compatible with the most common Real-Time PCR systems and DNA extraction and purification systems.

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Hepatitis E Diagnostic Test
quanty HEV

Hepatitis E is a liver infection caused by the hepatitis E virus (HEV) and the most sensitive method for confirming a diagnosis of HEV is the use of Real-Time PCR. The quanty HEV system is an in vitro diagnostic test for identification and quantification of Hepatitis E genome, by one-step RT-PCR Real-Time.

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Monkeypox Test
quanty Monkeypox Kit

The quanty Monkeypox system is a quantitative test that allows the DNA amplification and quantification, by means of Real-Time PCR, of the 2022 Monkeypox virus genome. It can detect the MPXV genome and also discriminate the two MPXV clades (West Africa and Congo basin) from biological samples such as swabs from skin lesions.

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Real Time Legionella Pneumophila Detection Kit
Duplicα

The Duplicα Real Time Legionella Pneumophila detection kit is an in vitro diagnostic test for the detection of Legionella pneumophila, by Real-Time PCR. It uses respiratory specimens and is compatible with most common Real Time PCR systems.

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Hepatitis A RT-PCR Test
quanty HAV

The quanty HAV system is an in vitro diagnostic test for identification and quantification of Hepatitis A genome, by one-step RT-PCR Real-Time. It requires plasma and serum diagnostic samples and can be run on Applied Biosystems 7500 Fast (ThermoFisher Scientific) and Rotor-Gene Q MDx (RG-Q MDx - QIAGEN).

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Lactose Intolerance Test
Lactose Intolerance LCT Kit

The lactose intolerance LCT Kit is a qualitative test that allows the allelic discrimination, by Real-Time PCR, of C13910T polymorphism associated to lactose intolerance. The procedure allows the amplification of the two allelic variants for the polymorphism discriminating the three possible genotypes: Homozygote Wild-Type, Homozygote Mutated and Heterozygote Mutated.

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Mycoplasma Pneumoniae Test
Duplicα RealTime Mycoplasma Pneumoniae Detection Kit

Duplicα RealTime Mycoplasma pneumoniae Detection Kit is an in vitro diagnostic test for the detection of Mycoplasma pneumoniae DNA by Real-Time PCR. It requires respiratory samples and is compatible with common real-time PCR Systems as well as DNA extraction and purification systems.

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Nucleic Acid Purification System
CloNext 24

The CloNext 24 fully-automated nucleic acid purification system is designed for fast, high-purity, high-yield nucleic acids & cell purification from a wide range of sample types for molecular diagnostic, biological diagnostic and clinical diagnostic. Its features include a compact, user friendly and intuitive interface, pre-loaded protocols with free upgrades, and a full kits and samples traceability system with end-run complete report in compliance with 21 CFR part 11 regulation.

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Nucleic Acid Purification System
CloNext 12

The CloNext 12 fully-automated nucleic acid purification system is designed for fast, high-purity, high-yield nucleic acids & cell purification from a wide range of sample types for molecular diagnostic, biological diagnostic and clinical diagnostic. Its features include a compact, user friendly and intuitive interface, pre-loaded protocols with free upgrades, and a full kits and samples traceability system with end-run complete report in compliance with 21 CFR part 11 regulation.

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COVID-19 Kit CE-IVD
quanty COVID-19v2

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FluA/FluB/SARS-CoV-2 Kit
FluA/FluB/SARS-CoV-2

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COVID-19 Real Time PCR Test
COVID-19 HT Screen (RT-25HT)

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COVID-19 Variant Detection Kit
COVID-19 Variant Catcher

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Cuidados intensivos Medicina de emergencia
Cuidados intensivos
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Sistemas de Anestesiología

Cuidados domiciliarios Rehabilitación
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Infraestructura hospitalaria Equipamiento TI
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Imágenes medicas Tomografía computarizada
Radiografía Digital
Sistemas de gestión de imágenes
Radiología intervencionista
Imágenes por resonancia magnética
Mamografía
PACS / RIS
Tomografía de emisión de positrones
Seguridad de las radiaciones
Radiografía
Tomografía computarizada de emisión de fotón único
Ultrasonido
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Atención al paciente Cuidado bariátrico
Camas
Equipos de examen
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Cirugía Endoscopia
Laparoscopia
Cirugía laser
Equipamiento de quirófano
Esterilización
Implantes quirúrgicos
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Laboratorio clínico Analizadores de Sangre y Gas
Contadores de Células
Centrífugas
Analizador de Química Clínica
Analizadores de Coagulación
Laboratorio General
Analizadores de Hematología
Sistemas de Inmunoensayo
Cristalería de Laboratorio
Lector de Microplacas
Microscopios
Pipetas
Pruebas Rápidas
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Analizador de Orina

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CLONIT SRL

CLONIT SRL

Covid-19 CLONIT SRL

Laboratorio clínico

Sobre CLONIT SRL

Actualizado

Laboratorio clínico