Shop All Clinical Analyzers and Instruments

Genomics and Proteomics


Analytical Method


Certifications/Compliance


Detectable Analytes


Height (English) Exterior


Height (Metric) Exterior


Length (English) Exterior


Length (Metric) Exterior


Length (Metric) Gel


Max. Networked Workstations


Product Type


Shelf Life


Storage Requirements


Volume (Metric) Buffer


Width (English) Exterior


Width (Metric) Exterior


Width (Metric) Gel

Ion AmpliSeq™ Exome RDY Kit 1x8 Ion Torrent™

The Ion AmpliSeq Exome RDY Kit enables the fastest and simplest method of exome enrichment, now even easier with oligo pools for ultra-high multiplex PCR exome enrichment dried down in a 96-well plate. With half the number of target amplification pipetting steps compared to the original protocol and the elimination of small pipetting volumes, exome libraries can now be produced with unparalleled ease in under six hours with less than 50 minutes of hands-on time. Also, the Ion AmpliSeq Exome RDY Kit is compatible with the Ion Library Equalizer Kit for ease in library normalization. Leveraging the ultra-high multiplex PCR approach of Ion AmpliSeq technology with template preparation on the Ion Chef System and sequencing on an Ion Proton or Ion S5 System, the Ion AmpliSeq Exome RDY Kit allows for rapid sequencing of key exonic regions of the genome, going from DNA to variants in just two days.

The Ion AmpliSeq Exome RDY Kit 1x8 configuration includes the following components for eight exomes (two exomes per Ion PI v3 chip or Ion 540 Chip, and four exomes per Ion 550 Chip):

• Ion AmpliSeq Exome RDY panel: dried down oligo pools/primers in one 96-well plate with all eight rows filled (1x8), for ultra-high multiplex PCR enrichment of the exonic regions of the genome
• Ion AmpliSeq Library Kit Plus (8 exomes) for robust library preparation of Ion AmpliSeq Exome libraries using Ion AmpliSeq technology

The Ion AmpliSeq Exome RDY Kit enables you to:
• Simplify exome enrichment through the combination of dried-down primers and the Ion AmpliSeq workflow, with less than one hour of hands-on time and less than six hours total time
• Accelerate your disease research with rapid exome sequencing—DNA to variants in just two days
• Access affordable exome sequencing—no need to wait and batch dozens of samples or otherwise spend the high price of a lower-throughput run
• Maximize sequencing efficiency due to high performance specifications—designs covering >97% of the Consensus Coding Sequences (CCDS), >90% base on-target, and >90% coverage uniformity
• Identify annotated, filtered variants without bioinformatics expertise through fully integrated analysis with Torrent Suite and Ion Reporter software

Quickest exome enrichment with unprecedented simplicity
The Ion AmpliSeq Exome RDY Kit 1x8 configuration provides unmatched simplicity for exome enrichment. Primers have been dried down in a 96-well plate, using the 12 wells of a single row for each of the 12 primer pools, leading to the use of one row per exome. The Ion AmpliSeq Exome RDY S5 Kit 1x8 configuration contains a single 96-well plate, containing eight rows pre-filled with dried down primers, sufficient to prepare eight exome libraries. Additionally, the dried-down primers contain a light blue dye for easy identification of used or occupied rows. With a workflow requiring less than 50 minutes of hands-on time and no centrifugation steps, the kit enables exome library preparation in less than six hours. Additionally, the Ion AmpliSeq Exome RDY Kit maintains a low input requirement of 50 ng DNA. With the included Ion AmpliSeq Library Kit Plus, exome library preparation is more robust, resulting in higher uniformity and consistently higher library yield when performing library amplification. Also, the Ion AmpliSeq Exome RDY Kit is now compatible with the Ion Library Equalizer Kit for ultimate ease in library normalization.

Lowest cost per exome using a benchtop sequencer
The Ion AmpliSeq Exome RDY Kit allows disease researchers to access affordable exome sequencing on their benchtops without long turn-around times or the sample batching normally required to achieve a low cost per sample. Using the Ion AmpliSeq Exome RDY Kit with the Ion Proton or Ion S5 System enables you to go from DNA to variants in as little as two days. Additionally, with the most uniform exome enrichment covering >97% of the CCDS, you can achieve the most efficient sequencing with two exomes per Ion PI or Ion 540 Chip and four exomes per Ion 550 Chip.

Fully integrated analysis without bioinformatics expertise
Use of the kit with Torrent Suite and Ion Reporter software provides a simple and streamlined analysis workflow that automates the identification of your variants of interest without needing the expertise or infrastructure of a full bioinformatics team. Additionally, the Ion Proton or Ion S5 Sequencer along with Ion Reporter Software deliver both SNP and indel information along with copy number changes through a single analysis workflow, advancing your human disease research.

Ion AmpliSeq™ Exome RDY Kit 4x2 Ion Torrent™

The Ion AmpliSeq Exome RDY Kit enables the fastest and simplest method of exome enrichment, now even easier with oligo pools for ultra-high multiplex PCR exome enrichment dried down in a 96-well plate. With half the number of target amplification pipetting steps compared to the original protocol and the elimination of small pipetting volumes, exome libraries can now be produced with unparalleled ease in under six hours with less than 50 minutes of hands-on time. Also, the Ion AmpliSeq Exome RDY Kit is compatible with the Ion Library Equalizer Kit for ease in library normalization. Leveraging the ultra-high multiplex PCR approach of Ion AmpliSeq technology with template preparation on the Ion Chef System and sequencing on the Ion Proton or Ion GeneStudio S5 next-generation sequencers, the Ion AmpliSeq Exome RDY Kit allows for rapid sequencing of key exonic regions of the genome, going from DNA to variants in just two days.

The Ion AmpliSeq Exome RDY Kit 4x2 configuration includes the following components for eight exomes (two exomes per Ion PI v3 chip or Ion 540 Chip, and four exomes per Ion 550 Chip):

• Ion AmpliSeq Exome RDY panel: dried down oligo pools/primers in four 96-well plates, each with two rows (C and F) filled (4x2), for ultra-high multiplex PCR enrichment of the exonic regions of the genome
• Ion AmpliSeq Library Kit Plus (8 exomes) for robust library preparation of Ion AmpliSeq Exome libraries using Ion AmpliSeq technology

The Ion AmpliSeq Exome RDY Kit enables you to:
• Simplify exome enrichment through the combination of dried-down primers and the Ion AmpliSeq workflow, with less than one hour of hands-on time and less than six hours total time
• Accelerate your disease research with rapid exome sequencing—DNA to variants in just two days
• Access affordable exome sequencing—no need to wait and batch dozens of samples or otherwise spend the high price of a lower-throughput run
• Maximize sequencing efficiency due to high performance specifications—designs covering >97% of the Consensus Coding Sequences (CCDS), >90% base on-target, and >90% coverage uniformity
• Identify annotated, filtered variants without bioinformatics expertise through fully integrated analysis with Torrent Suite and Ion Reporter software

Quickest exome enrichment with unprecedented simplicity
The Ion AmpliSeq Exome RDY Kit 4x2 configuration provides unmatched simplicity for exome enrichment. Primers have been dried down into 96-well plates, using the 12 wells of a single row for each of the 12 primer pools, leading to the use of one row per exome. The Ion AmpliSeq Exome RDY S5 Kit 4x2 configuration contains four 96-well plates, each with two rows pre-filled with dried-down primers, sufficient to prepare eight exome libraries. Additionally, the dried-down primers contain a light blue dye for easy identification of used or occupied rows. With a workflow requiring less than 50 minutes of hands-on time and no centrifugation steps, the kit enables exome library preparation in less than six hours. Additionally, the Ion AmpliSeq Exome RDY Kit maintains a low input requirement of 50 ng DNA. With the included Ion AmpliSeq Library Kit Plus, exome library preparation is more robust, resulting in higher uniformity and consistently higher library yield when performing library amplification. Also, the Ion AmpliSeq Exome RDY Kit is now compatible with the Ion Library Equalizer Kit for ultimate ease in library normalization.

Lowest cost per exome using a benchtop sequencer
The Ion AmpliSeq Exome RDY Kit allows disease researchers to access affordable exome sequencing on their benchtops without long turn-around times or the sample batching normally required to achieve a low cost per sample. Using the Ion AmpliSeq Exome RDY Kit with the Ion Proton or Ion S5 System enables you to go from DNA to variants in as little as two days. Additionally, with the most uniform exome enrichment covering >97% of the CCDS, you can achieve the most efficient sequencing with two exomes per Ion PI or Ion 540 Chip and four exomes per Ion 550 Chip.

Fully integrated analysis without bioinformatics expertise
Use of the kit with Torrent Suite and Ion Reporter software provides a simple and streamlined analysis workflow that automates the identification of your variants of interest without needing the expertise or infrastructure of a full bioinformatics team. Additionally, the Ion Proton or Ion S5 Sequencer along with Ion Reporter Software deliver both SNP and indel information along with copy number changes through a single analysis workflow, advancing your human disease research.

G5v2 Module CD for 310 Genetic Analyzer Applied Biosystems™

This is a G5v2 Module for use in the 310 Genetic Analyzer.

For Research Use Only. Not for use in diagnostics procedures.

TaqMan™ Array, Human IGF-1R Signaling, Fast 96-well Applied Biosystems™

These 96-well plates are pre-configured with the most appropriate TaqMan® Gene Expression Assays for a specific biological process, pathway, or disease state. Each plate contains predefined assays and endogenous controls dried-down in the wells, ready for accurate assessment of an entire gene signature in one simple experiment. The TaqMan® Array Human IGF1R Signaling 96-well Plate contains 92 assays to genes associated with IGF1R signaling and 4 assays to candidate endogenous control genes.

MagMAX™ CORE Nucleic Acid Purification Kit Applied Biosystems™

The MagMAX CORE Nucleic Acid Purification Kit is a highly-effective solution for purifying RNA and DNA from an expansive range of veterinary sample types. The universal chemistry is optimized for use on a variety of KingFisher magnetic particle processors and the kit's modular design enables flexibility to evolve with future testing needs. The MagMAX CORE kit helps to streamline laboratory workflows for downstream real-time PCR, RT-PCR, and sequencing applications.

The MagMAX CORE Nucleic Acid Purification Kit offers:
• Pre-mixed, room-temperature reagents, greatly improving product handling and storage
• Minimal extraction and reagent preparation time, to get diagnostic results more quickly
• Complete workflows that address 14 unique sample types, providing a universal sample preparation solution
• A single protocol adapted on multiple KingFisher magnetic particle processors, unifying all workflows regardless of throughput

Accelerate
The MagMAX CORE Nucleic Acid Purification Kit provides faster instrument processing times, allowing for diagnostic results more quickly. The kit needs less preparation time, due to pre-mixed washes that do not require the addition of alcohols. The MagMAX CORE workflow provides higher-quality nucleic acids than other on-market chemistries, which leads to fewer workflow interruptions and greater diagnostic sensitivity.

Optimize
The MagMAX CORE Nucleic Acid Purification Kit requires less KingFisher plastics, eliminating unnecessary waste and costs. All kit reagents are stored at room temperature, greatly improving product handling and saving on storage space and costs. The MagMAX kit operates using a single protocol adapted on multiple KingFisher magnetic particle processors, unifing workflows regardless of throughput. The chemistry is optimized to address 15 unique sample types, including:

• Whole blood
• Feces
• Oral fluid
• Animal, fecal, and environmental swabs
• Tissue
• Milk
• Hair follicles
• Semen
• Serum
• Ear notches
• Ear punches
• Environmental samples
• BioMed Diagnostics InPouch TF (Tritrichomonas foetus) culture
• Plasma

Evolve
The MagMAX CORE Nucleic Acid Purification Kit is designed to be the last sample preparation you may ever need to validate. It utilizes a ‘CORE’ chemical formulation and couples easily to flexible modules, introducing new applications without introducing new chemistries. The novel MagMAX CORE kit formulation and workflow prepares samples for downstream sequencing applications.

BRKT, System Power Supply Applied Biosystems™

This is a spare part for the 310 Genetic Analyzer.

For Research Use Only. Not for use in diagnostics procedures.

GlobalFiler™ Express PCR Amplification Kit Applied Biosystems™

The GlobalFiler Express PCR Amplification Kit is the first 6-dye, 24-locus STR kit that combines maximum compatibility with global databasing loci standards, with dramatically reduced amplification time and superior discrimination power, to enable forensic DNA labs worldwide to maximize information recovery and improve overall efficiency. The GlobalFiler Express kit is part of a fully integrated and validated forensic DNA workflow backed by best-in-class global training, service, and support. This kit is optimized for database and single-source samples; for casework samples, please see our GlobalFiler PCR Amplification Kit.

Key Features:

• Up to 5-times faster amplification time than previous-generation kits
• DNA results in <2 hours—using current CE platforms
• Optimized protocols for blood and buccal samples deposited on swab or paper substrates
• The only kit with all markers recommended for inclusion by the CODIS Core Loci Working Group, including all markers commonly used in Europe, for maximum global database compatibility

The GlobalFiler Express kit is a robust and reliable single-amplification STR multiplex kit optimized for use with database and single-source samples. The kit leverages new dyes for the incorporation of additional markers, generating the most discriminating kit available to the forensic community. The kit contains all of the markers included in the major global databases and utilizes optimized reagents, thermal cycling parameters, and the latest advances in oligo synthesis and purification to enable the highest quality results specific to the sample type being processed. Maintenance of the NGM SElect and Identifiler primer sequences helps to ensure maximum concordance with previously typed samples. In addition, multiple gender markers have been added to the multiplex to enable accurate typing of male samples, even highly degraded or Y-negative samples, while increased genotyping accuracy is obtained with the expansion of the allelic ladder allele ranges to include all rare alleles as described in the literature (STRbase).

Experience Matters
We are the only company in the world that designs and validates its reagents, instruments, and data analysis software together as an integrated system for DNA testing. Technical service scientists and field application specialists are available to answer your technical questions, review data, and make recommendations on how to perform assays and troubleshoot results. All of these resources help ensure success when using Applied Biosystems human identification solutions in your laboratory.

Clariom™ D Assay, human Applied Biosystems™

Accelerate your biomarker discovery from deep within the transcriptome with Clariom D Assays for human samples, the next generation of transcriptome-level expression profiling tools. Clariom D Assays provide a highly detailed view of the transcriptome and offer the fastest path to the results you need for your research. Clariom D Assays allow translational research scientists to generate high-fidelity biomarker signatures quickly and easily. Based on industry-leading microarray technology, the novel design of these assays provides the most intricate transcriptome-wide gene- and exon-level expression profiles, including the ability to detect alternative splicing events of coding and long non-coding (lnc)RNA, in a single three-day experiment.

Expand your potential to discover novel, informative biomarkers
The number of known transcribed genes has expanded rapidly in recent years, providing more sources for actionable biomarkers, such as transcript variants and lncRNA, that can be used for clinical utility and advancing our understanding of disease mechanisms. Such biomarkers can be missed by lengthy, complex, and costly sequencing and targeted expression approaches, leading to irreproducible signatures and wasted time and money.

With full coverage of the transcribed genome including all known coding and non-coding splice variants, compatibility with clinical sample types, and flexible data analysis software, Clariom D assays are the premier tools for translational researchers performing complex expression biomarker discovery studies and wanting the fastest path to robust, clinically relevant, and actionable results.

Get all the data you need
• Rapidly identify complex disease signatures from >540,000 transcripts sourced from the largest number of public databases, the most comprehensive coverage of the human transcriptome available, to ensure biomarkers are not missed.
• Confidently detect genes, exons, and alternative splicing events that give rise to coding RNA and lncRNA isoforms.
• Detect rare and low-expressing transcripts otherwise not detected by common sequencing approaches.
• Go from data to insight in minutes with intuitive, highly visual, free analysis software.
When you have precious samples, get it right the first time.

• Utilize RNA from various sample types including blood, cells, and fresh/fresh-frozen tissues.
• Preserve sample integrity and reduce data variability with an assay that does not require a globin or rRNA removal step.

Clariom D solutions are available in a single sample (cartridge array) format for use on the GeneChip™ 3000 instrument system and include reagents and fast, simple Transcriptome Analysis Console (TAC) software to analyze and visualize global expression patterns of genes, exons, pathways, and alternative splicing events.

Get the coverage you require, the reproducibility you need, and the insights you want to act on your discoveries.

TaqMan™ Array, Human IL-1 Pathway, Fast 96-well Applied Biosystems™

These 96-well plates are pre-configured with the most appropriate TaqMan® Gene Expression Assays for a specific biological process, pathway, or disease state. Each plate contains predefined assays and endogenous controls dried-down in the wells, ready for accurate assessment of an entire gene signature in one simple experiment. The TaqMan® Array Human IL-1 Pathway 96-well Plate contains 44 assays to IL-1 pathway associated genes and 4 assays to candidate endogenous control genes. All assays are plated in duplicate.

Gallery Reagents for Food and Beverage Analysis Thermo Scientific™

Save time by eliminating reagent preparation with the Thermo Scientific™ Gallery™ system reagents for food and beverage analysis. Over 50 ready-to-use gallery system reagents are offered for food and beverage analysis, with the kits including two to four reagents in 20 mL barcoded vials. This enables the necessary identification data, such as lot numbers and expiration dates, to be read automatically by the discrete analyzer's barcode reader. Automated dilutions make it possible to apply methods for a wide range of analyte concentrations. Save time and reduce errors by simplifying your analysis with the Gallery system reagents.

ASSY, CBL Encoder Applied Biosystems™

This is a spare part for the 310 Genetic Analyzer.

For Research Use Only. Not for use in diagnostics procedures.

GeneMapper™ ID Software v3.3 Initial License Applied Biosystems™

GeneMapper® ID Software version 3.3 (Simplified Chinese Version) and the AmpFLSTR® Sinofiler™ PCR Amplification Kit are designed specifically to meetthe needs of Chinese forensic DNA laboratories. When used together as part of an integrated solution, GeneMapper® ID Software version 3.3 and the AmpFLSTR® Sinofiler™ PCR Amplification Kit provide the necessary functionality and flexibility to address the diverse challenges faced when processing forensic casework and high volume convicted offender DNA samples.

• Contains new version (v2_33) of panel and binset files that support the new AmpFLSTR® Sinofiler™ PCR Amplification Kit, as well as previously supported AmpFLSTR® kits
• Automatically imports the panel and binset files and eliminates the need to manually import the panel and binset
• All static user interfaces translated in Simplified Chinese
• GeneMapper® ID Software v3.3 has the same analysis algorithms as GeneMapper® ID Software v3.2.1

Reduce Analysis Bottlenecks
The software's novel Process Component-Based Quality Values (PQVs) enable you to identify and sort genotypes quickly based on user-defined quality thresholds. Check the concordance of overlapping controls and loci from different AmpFLSTR® kits automatically -- significantly improving analysis workflow and productivity.

A Complete, Verified System
GeneMapper® ID Software v3.2.1 is an integral component of Applied Biosystems complete system of instruments, reagents, software, and service for human-identity applications. It has undergone extensive verification testing to ensure robust design features, performance, and reproducibility you can depend on.

5500xl to 5500xl-W with PC upgrade Applied Biosystems™

This is an optical and computer upgrade kit for the 5500xl Genetic Analyzer for conversion to a 5500xl-W system.

The 5500xl-W Genetic Analyzer helps achieve optimal productivity with a faster workflow, two flexible FlowChips, intuitive user workflows, and project scalability. Faster turn-around times are achieved through the introduction of a non-bead based workflow and increased throughput with a combination of higher colony density and improved optics. The 5500xl-W Genetic Analyzer offers these improvements while maintaining the benefits of the 5500 and 5500xl systems: accuracy, sensitivity, and cost effectiveness. With the 5500xl-W Genetic Analyzer, you are empowered to discover rare genetic events or sub-populations of somatic mutations at an unprecedented pace.

Key Benefits:
• Sequencing right here, right now
• Cost-effective sequencing runs with individually configurable lanes
• Superior low-frequency variant detection for whole-exome sequencing or targeted resequencing
• Reproducibility, reliability, and quality for your RNA applications
• Confidence and uniformity in multiplexing with up to 96 barcodes
• Optimal analysis solutions for streamlined productivity and freedom to operate
• New non-bead based workflow for improved project turnaround and efficiency

When Coverage is Not Enough
Additional sequence coverage fails to compensate for poor accuracy in the detection of rare variants that may hold the key to a better understanding cancer progression, disease penetrance, or drug resistance. With a system accuracy of up to 99.999%, the 5500xl-W Genetic Analyzer enables you to perform 25% less sequencing to detect rare variants than a next-generation sequencing platform with 99.99% system accuracy in order to detect somatic variant present at 1% (Figure 2). The industry-leading accuracy of the 5500xl-W Genetic Analyzer enables detection of significant biological variation for applications like whole genome resequencing, targeted resequencing, and whole transcriptome analysis.

When Flexibility, Speed, and Cost are Crucial
Multidisciplinary translational research programs often require processing of multiple samples across multiple applications like whole exome, RNA-seq, and structural variation. The 5500xl-W Genetic Analyzer provides you the flexibility to configure your sequencing runs to your project and throughput needs (Figure 3). The system’s two configurable microfluidic FlowChips process 6–12 independent samples, and the intelligent barcoding kits multiplex up to hundreds of samples in a single run. Pay-Per-Lane Sequencing (PPL-Seq™) and independent run lanes tailor the system to any project scale. The new non-bead based workflow shaves 1–2 days off project workflows for faster project data delivery. Increased colony density coupled with improved optics provides more data from each lane. With the 5500xl-W Genetic Analyzer, avoid project delays by optimizing your run configurations to attain the lowest cost per sample.

When the Utmost Productivity and Efficiency are Essential
Ease of use, quality control, and speed are integral components of any next-generation sequencing workflow. Co-developed with Hitachi-Hi Technologies, the 5500xl-W Genetic Analyzer's elegant tabletop design (Figure 1) is built off “Six-Sigma' processes to streamline your research. The 5500xl-W Genetic Analyzer delivers streamlined fluidics and a simple, intuitive graphical user interface (GUI) for easy setup and run monitoring. Real-time analysis and 60% smaller data footprints expedite data export and analysis time. Additionally, with embedded sequencing controls and reagent usage tracking, the 5500xl-W Genetic Analyzer empowers you to obtain extremely high-quality and biologically-meaningful data out of every sequencing run.

Take Comprehensive Research to New Heights
The superior accuracy, flexibility, and productivity of the 5500xl-W Genetic Analyzer accelerate comprehensive research. Larger translational medicine initiatives, genome consortiums, and disease-subtype stratification projects with resulting groundbreaking publications are now within your grasp. Catch them all with the 5500xl-W Genetic Analyzer.

A Community of Support
With more than 2,000 field personnel, we have the most extensive network of dedicated Field Application Specialists and Service Engineers to work with you, so that you can feel confident that we will be there when and where you need us most.

This product includes:
Scientific CMOS camera and tube lens assembly
New high efficiency objective lens
Mounting accessories and communication cables
NextIO vCore Express
GPU and RAM upgrades, communication cables

GeneChip™ 3' IVT PLUS Reagent Kit Applied Biosystems™

The GeneChip™ 3' IVT PLUS Reagent Kit features:
• Low RNA input requirements – as little as 50 ng total RNA input for a single round of amplification to leave more samples for further studies
• Expression assay kit – GeneChip 3' IVT Express Kit (3' IVT Express Kit) for continuation of high-quality of data generation without compromising the legacy data
• Protocol optimization with no initial primer annealing or cDNA purification step for a streamLined workflow
• Single-day protocol with appropriate inputs of total RNA for rapid sample processing
• Magnetic bead purification for enhanced recovery to generate sufficient target
• Built-in controls to assist in effective trouble shooting
With enhanced performance, fewer required reagents, and a simple protocol, target preparation has never been so easy.

3' IVT PLUS Kit includes:
• All reagents needed to generate and label aRNA target
• Ready to use magnetic bead purification for enhanced recovery
• Poly-A RNA controls
• Hyb controls
• Tubes organizer for quick assay set up

About Poly-A controls
Poly-A controls (lys, phe, thr, and dap) monitor the target labeling process from start to finish. They serve as sensitivity indicators of target prep and labeling efficiency. This kit contains four exogenous, pre-mixed, poly-adenylated prokaryotic controls that are spiked directly into RNA samples before target labeling. Their resultant signal intensities on Applied Biosystems GeneChip Arrays serve as indicators of the labeling reaction efficiency.

About Hyb controls
The 20X Eukaryotic hybridization controls are comprised of a mixture of biotinylated and fragmented cRNA of bioB, bioC, bioD, and cre in staggered concentrations, ready to be added directly to the hybridization cocktail. These controls facilitate monitoring of the hybridization process for troubleshooting. Control Oligo B2 is included to provide alignment signals for image analysis.

Indiko™ Plus Clinical Chemistry Analyzer Thermo Scientific™

Experience an uncompromised level of performance and ease of use with the Thermo Scientific™ Indiko™ Plus Clinical Chemistry Analyzer. This fully-automated random access benchtop system for clinical and specialty chemistry testing, combined with system reagents and consumables form a fully-supported, complete system solution offering confidence to daily work.
Results per page
    spinner