The MAGPIX Drive Fluid PLUS serves as the delivery medium that carries the sampl
The MAGPIX Drive Fluid PLUS serves as the delivery medium that carries the sample to the optics component of the MAGPIX instrument.
NSU
Instrumentation for clinical multiplex test systems
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip
The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection.
OCC,OZE,OZZ,OEM,OOU,OEP
Respiratory virus panel nucleic acid assay system,Influenza A and influenza B mu
Respiratory virus panel nucleic acid assay system,Influenza A and influenza B multiplex nucleic acid assay,Bordetella pertussis dna assay system,Human metapneumovirus (hmpv) rna assay system,Parainfluenza multiplex nucleic acid assay,Influenza a virus subtype differentiation nucleic acid assay
2
Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge
The Verigene® Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualita
The Verigene® Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualitative test for simultaneous detection and identification of common pathogenic enteric bacteria, viruses, and genetic virulence markers from liquid or soft stool preserved in Cary-Blair medium, collected from individuals with signs and symptoms of gastrointestinal infection.
The Verigene® Processor is an instrument which internalizes all of the functions
The Verigene® Processor is an instrument which internalizes all of the functions required to process a Test Cartridge as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications.
NSU
Instrumentation for clinical multiplex test systems
The Verigene® Processor SP is an instrument which integrates sample preparation,
The Verigene® Processor SP is an instrument which integrates sample preparation, target amplification, and target hybridization within a single device as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished)
NSU,OOI
Instrumentation for clinical multiplex test systems,real time Nucleic acid ampli
Instrumentation for clinical multiplex test systems,real time Nucleic acid amplification system
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
xMAP Control Microspheres, Classification (CON1) and Reporter (CON2), are polyst
xMAP Control Microspheres, Classification (CON1) and Reporter (CON2), are polystyrene microspheres that are internally labeled with fluorescent dyes. The control microspheres are intended to verify the calibration and optical integrity for the Luminex 100/200 System. Classification Control Microspheres verify both classification channels and the doublet discriminator channel (DD). Reporter Control Microspheres verify the reporter channel.
NSU
Instrumentation for clinical multiplex test systems
The Luminex MAGPIX Performance Verification Kit is intended to verify the optica
The Luminex MAGPIX Performance Verification Kit is intended to verify the optical calibration of the MAGPIX instrument.
NSU
Instrumentation for clinical multiplex test systems
The Luminex MAGPIX Calibration Kit is intended to calibrate the optics of the MA
The Luminex MAGPIX Calibration Kit is intended to calibrate the optics of the MAGPIX instrument. During calibration, the system adjusts LED current and calibration factors for CL1, CL2, and RP1 until those values match the imported target values, thus calibrating the classification map.
NSU
Instrumentation for clinical multiplex test systems
The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualit
The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal swabs (NPS) specimens from patients with signs and symptoms of respiratory tract infection in conjunction with clinical and laboratory findings.
OZE,OCC
Influenza A and influenza B multiplex nucleic acid assay,Respiratory virus panel
Influenza A and influenza B multiplex nucleic acid assay,Respiratory virus panel nucleic acid assay system
The ARIES® M1 System is a clinical multiplex test system that automates and inte
The ARIES® M1 System is a clinical multiplex test system that automates and integrates extraction of nucleic acid from a clinical sample, performs real -time PCR, and measuring and sorting multiple signals generated in an in vitro diagnostic assay.
The VERIGENE® II System is an in vitro diagnostic (IVD) platform that performs n
The VERIGENE® II System is an in vitro diagnostic (IVD) platform that performs nucleic acid based tests in clinical laboratories. The VERIGENE II System is capable of automated extraction and purification of nucleic acids from multiple sample types as well as automated amplification, array hybridization, and detection of target nucleic acid sequences.
NSU
Instrumentation for clinical multiplex test systems
The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip
The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection.
OEP,OCC,OZZ,OZE,OEM,OOU
Influenza a virus subtype differentiation nucleic acid assay,Respiratory virus p
Influenza a virus subtype differentiation nucleic acid assay,Respiratory virus panel nucleic acid assay system,Bordetella pertussis dna assay system,Influenza A and influenza B multiplex nucleic acid assay,Human metapneumovirus (hmpv) rna assay system,Parainfluenza multiplex nucleic acid assay
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
OLD
Internal polymerase chain reaction control, not assay specific
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
The ARIES® Extraction Kit is intended to extract nucleic acid from human biologi
The ARIES® Extraction Kit is intended to extract nucleic acid from human biological specimens and universal transport media (UTM).
A concentrated version of xMAP® Sheath Fluid PLUS, when diluted is is the delive
A concentrated version of xMAP® Sheath Fluid PLUS, when diluted is is the delivery medium of the sample to the optics component.
NSU
Instrumentation for clinical multiplex test systems
The Verigene® Clostridium difficile Nucleic Acid Test (CDF) is a qualitative mul
The Verigene® Clostridium difficile Nucleic Acid Test (CDF) is a qualitative multiplexed in vitro diagnostic test for the rapid detection of toxin A (tcdA), toxin B (tcdB), and tcdC gene sequences of toxigenic Clostridium difficile and for presumptive identification of PCR ribotype 027 strains from unformed (liquid or soft) stool specimens collected from patients suspected of having C. difficile infection (CDI).
The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed us
The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed using the sample-to-result Verigene® System, is a qualitative multiplexed in vitro diagnostic test for the simultaneous detection and identification of selected gram-negative bacteria and resistance markers.
PEN
Gram-Negative bacteria and associated resistance markers
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
Nucleic acid sequences, which, through specific binding or chemical reaction wit
Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens
The ARIES® HSV 1 & 2 Assay is a polymerase chain reaction (PCR)-based qualitativ
The ARIES® HSV 1 & 2 Assay is a polymerase chain reaction (PCR)-based qualitative in vitro diagnostic test for the direct detection and differentiation of herpes simplex virus (HSV) DNA from cutaneous and mucocutaneous lesion swab specimens.
PGI
Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutane
Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutaneous lesion samples
The Verigene® Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed us
The Verigene® Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene® System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria which may cause bloodstream infection (BSI).
NQX,PAM
SYSTEM, NUCLEIC ACID AMPLIFICATION TEST, DNA, METHICILLIN RESISTANT STAPHYLOCOCC
SYSTEM, NUCLEIC ACID AMPLIFICATION TEST, DNA, METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS, DIRECT SPECIMEN,Gram-positive bacteria and their resistance markers
The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed us
The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed using the sample-to-result Verigene® System, is a qualitative multiplexed in vitro diagnostic test for the simultaneous detection and identification of selected gram-negative bacteria and resistance markers.
PEN
Gram-Negative bacteria and associated resistance markers
2
Gram-Negative Blood Culture (BC-GN) Nucleic Acid Test Cartridge
The ARIES® Group A Strep Assay is a real-time polymerase chain reaction (PCR) ba
The ARIES® Group A Strep Assay is a real-time polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection of Streptococcus pyogenes (Group A ß-hemolytic Streptococcus) in throat swab specimens from patients with signs and symptoms of pharyngitis.
PGX,OOI
Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system
Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system,real time Nucleic acid amplification system
The MAGPIX Drive Fluid serves as the delivery medium that carries the sample to
The MAGPIX Drive Fluid serves as the delivery medium that carries the sample to the optics component of the MAGPIX instrument.
NSU
Instrumentation for clinical multiplex test systems
The MultiCode®-RTx Herpes Simplex Virus 1 & 2 Kit is a polymerase chain reaction
The MultiCode®-RTx Herpes Simplex Virus 1 & 2 Kit is a polymerase chain reaction (PCR)-based qualitative in vitro diagnostic test for the detection and typing of herpes simplex virus (HSV 1 & 2) DNA in vaginal lesions. It is indicated for use in the detection and typing of HSV-1 or HSV-2 in vaginal lesion swab specimens from symptomatic female patients as an aid in the diagnosis of genital herpes infection.
The SYNCT Software is a desktop application that can be utilized by an end-user
The SYNCT Software is a desktop application that can be utilized by an end-user on a standalone computer, providing users the ability to operate general functions such as Order Management, with or without a Laboratory Information System (LIS), viewing test results, reviewing and preparing test reports, performing software administrative functions, and providing security control for permitted functions.
The Verigene® Reader is the central control of the Verigene® System, a benchtop
The Verigene® Reader is the central control of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications.
OOI,NSU
real time Nucleic acid amplification system,Instrumentation for clinical multipl
real time Nucleic acid amplification system,Instrumentation for clinical multiplex test systems
The ARIES® C. difficile Assay is a real-time polymerase chain reaction (PCR) bas
The ARIES® C. difficile Assay is a real-time polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection of Clostridium difficile (C. difficile) nucleic acid in unformed (liquid or soft) stool specimens obtained from patients suspected of having Clostridium difficile infection (CDI).
The Verigene® Hypercoagulation Panel Nucleic Acid Test contains the Verigene® F
The Verigene® Hypercoagulation Panel Nucleic Acid Test contains the Verigene® F5 Nucleic Acid Test, the Verigene® F2 Nucleic Acid Test and the Verigene® MTHFR Nucleic Acid Test. The Verigene® F5 Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (G to A at position 1691; also known as Factor V Leiden) of the human Factor V gene (F5; Coagulation Factor V gene) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples. The Verigene® F2 Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (G to A at position 20210) of the human Factor II gene (F2; prothrombin gene) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples. The Verigene® MTHFR Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (C to T at position 677) of the human 5,10 methylenetetrahydrofolate reductase gene (MTHFR) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples.
OMM,NPQ,NPR
Test 5, 10-methylenetetrahydrofolate reductase mutations, genomic dna pcr,TEST,
Test 5, 10-methylenetetrahydrofolate reductase mutations, genomic dna pcr,TEST, FACTOR V LEIDEN MUTATIONS, GENOMIC DNA PCR,TEST, FACTOR II G20210A MUTATIONS, GENOMIC DNA PCR
The ARIES® System is a clinical multiplex test system that automates and integra
The ARIES® System is a clinical multiplex test system that automates and integrates extraction of nucleic acid from a clinical sample, performs real -time PCR, and measuring and sorting multiple signals generated in an in vitro diagnostic assay.
The MGB Alert Internal Control MS2 RNA Template consists of an RNA bacteriophage
The MGB Alert Internal Control MS2 RNA Template consists of an RNA bacteriophage intended for use as an internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The MS2 Internal Control can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The internal control is not intended to monitor other real-time PCR processes.
MGB Alert MS2 Internal Control RNA Template (480uL volume)
The MGB Alert Internal Control MS2 DNA Template consists of a DNA plasmid intend
The MGB Alert Internal Control MS2 DNA Template consists of a DNA plasmid intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The MS2 Internal Control can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The internal control is not intended to monitor other real-time PCR processes.
MGB Alert MS2 Internal Control DNA Template (250uL volume)
The MGB Alert Internal Control IC2 Template consists of a DNA plasmid intended f
The MGB Alert Internal Control IC2 Template consists of a DNA plasmid intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The IC2 Internal Control can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The internal control is not intended to monitor other real-time PCR processes.
MGB Alert IC2 Internal Control Template (250uL volume)
The MGB Alert Internal Control IC2 Template consists of a DNA plasmid intended f
The MGB Alert Internal Control IC2 Template consists of a DNA plasmid intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The IC2 Internal Control can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The internal control is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control IC1 Template consists of a DNA plasmid intended f
The MGB Alert Internal Control IC1 Template consists of a DNA plasmid intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The IC1 Internal Control can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The internal control is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as an un-assayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1 can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
MGB Alert IC1 Internal Control Template (35uL volume)
The MGB Alert Internal Control Set IC1 DSQ contains the MGB Alert IC1 DNA Templa
The MGB Alert Internal Control Set IC1 DSQ contains the MGB Alert IC1 DNA Template, the MGB Alert IC1 v3.0 Primers, and the MGB AlertIC1 DSQ Probe. When used as intended, the Internal Control Set IC1 DSQ will detect systemic variation that may arise during the nucleic acidextraction and amplification processes associated with real-time PCR assays.
The MGB Alert Internal Control Set IC1 DSQ contains the MGB Alert IC1 DNA Templa
The MGB Alert Internal Control Set IC1 DSQ contains the MGB Alert IC1 DNA Template, the MGB Alert IC1 v3.0 Primers, and the MGB AlertIC1 DSQ Probe. When used as intended, the Internal Control Set IC1 DSQ will detect systemic variation that may arise during the nucleic acidextraction and amplification processes associated with real-time PCR assays.
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-C can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes. QTY-100@480 reactions.
MGB Alert Internal Control Set IC2-C -480 rxn QTY-100
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use as an un-assayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-C can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes. QTY-25@480 reactions.
MGB Alert Internal Control Set IC2-C -480 rxn QTY-25
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use as an un-assayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-B can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes. QTY-25@480 reactions.
MGB Alert Internal Control Set IC2-B, 480 rxn QTY-25
The MGB Alert Internal Control Set IC1-C consists of reagents intended for use a
The MGB Alert Internal Control Set IC1-C consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1-C can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes
The MGB Alert Internal Control Set IC2-H consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-H consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-H can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1-A consists of reagents intended for use a
The MGB Alert Internal Control Set IC1-A consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1-A can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1-V consists of reagents intended for use a
The MGB Alert Internal Control Set IC1-V consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1-V can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-C can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-C consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-C can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-B can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2 consists of reagents intended for use as
The MGB Alert Internal Control Set IC2 consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2 can be used to detect systemicvariation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is notintended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1 can be used to detect systemicvariation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is notintended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set MS2-E consists of reagents intended for use a
The MGB Alert Internal Control Set MS2-E consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set MS2-E can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set MS2-M consists of reagents intended for use a
The MGB Alert Internal Control Set MS2-M consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set MS2-M can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-B can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2 consists of reagents intended for use as
The MGB Alert Internal Control Set IC2 consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2 can be used to detect systemicvariation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is notintended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1 can be used to detect systemicvariation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is notintended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1-L consists of reagents intended for use a
The MGB Alert Internal Control Set IC1-L consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1-L can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-8 consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-8 consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-8 can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-T consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-T consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-T can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-T consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-T consists of reagents intended for use as an unassayed internal extraction and amplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-T can be used to detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is not intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1-A consists of reagents intended for use a
The MGB Alert Internal Control Set IC1-A consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1-A can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as
The MGB Alert Internal Control Set IC1 consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC1 can be used to detect systemicvariation that may arise during the extraction and amplification process associated with real-time PCR assays. The set is notintended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use a
The MGB Alert Internal Control Set IC2-B consists of reagents intended for use as an unassayed internal extraction and amplificationprocess control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-B can be used to detectsystemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. The set isnot intended to monitor other real-time PCR processes.
The MGB Alert Internal Control Set IC2-BH consists of reagents intended for use
The MGB Alert Internal Control Set IC2-BH consists of reagents intended for use as an unassayed internal extraction andamplification process control in any real-time polymerase chain reaction (PCR) assay. The Internal Control Set IC2-BH can be usedto detect systemic variation that may arise during the extraction and amplification process associated with real-time PCR assays. Theset is not intended to monitor other real-time PCR processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.
Internal control used in real-time polymerase chain reaction (pcr) assays to det
Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes.