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    PrepFiler Express/AutoMate Express™ Validation Applied Biosystems™

    This is a performance validation of the PrepFiler Express⁄AutoMate Express™ Forensic DNA Extraction System.

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

    Acetic Anhydride/Pyridine/THF, Capping Formula A Applied Biosystems™

    This acetic anhydride⁄tetrahydrofolate⁄pyridine (Cap A) solution comes in Trap-Pak™ bags. Trap-Pak™ bags are tightly sealed membrane packets containing molecular sieves to efficiently adsorb water. Use Trap-Pak™ bags to reduce and maintain a low water content in acetonitrile and tetrazole (activator) solutions.

    • Extensive testing and quality controls assure high quality reagents that meet our high expectations and specifications.
    • Reagents and supplies are use-tested and optimized for the 3900 system for quality nucleic acid synthesis.

    Tested
    Our high-performance reagents begin with raw materials that must conform to our strict specifications. Once the reagents are manufactured and packaged, extensive testing is performed to assure you that all liquids are free of interfering particulate matter; reagent concentrations are within our specifications, and the performance specification meets at least 98% stepwise coupling efficiency.

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

    Ion Xpress™ Plus Fragment Library Kit for AB Library Builder™ System Ion Torrent™

    The Ion Xpress™ Plus Fragment Library Kit for AB Library Builder™ System provides a rapid, flexible, and high-throughput solution for library construction upstream of the semiconductor sequencing workflow. This ready-to-use reagent cartridge simplifies next-generation sequencing by enabling automated DNA fragment library preparation for the Personal Genome Machine® and soon the Proton™ sequencing systems.

    This kit contains sample preparation reagents for enzymatic shearing and library construction of 13 DNA libraries for semiconductor sequencing. Use of this reagent cartridge requires the addition of library adapters (sold separately).

    This library kit offers:

    Simplicity and convenience of automated library preparation upstream of semiconductor sequencing
    Superior coverage uniformity for diverse sample types using our proprietary Ion Shear™ Plus chemistry
    Lower input requirement providing the ability to make amplification-free libraries from as little as 50 ng of starting DNA
    Rapid and flexible workflow producing Ion fragment libraries containing user-selectable and automatically size-selected insert sizes of 100–400 bp in as little as 2 hours
    Significant cost savings by removing the need for ancillary shearing devices and size-selection gels
    Scalable methodology to meet high-throughput sequencing requirements

    With its plug-n-play modular reagent design, this revolutionary kit automates all steps of library creation, including both DNA fragmentation and library size selection, in as little as 2 hours with limited set-up time and minimal subsequent user-intervention. DNA fragmentation is automated with enhanced, proprietary Ion Shear™ DNA fragmentation chemistry to achieve user-selectable inserts of 100–400 bp in length. Size selection of the libraries is performed automatically without the expense or effort of gel-based methods. Alternatively, libraries can be manually size-selected using conventional methods after the automated run. Starting with 50–1000 ng of input DNA, the kit yields significantly higher amounts of library than current manual methods, eliminating the need for PCR amplification (i.e., 'amplification-free' libraries) for most sequencing needs.

    A Single-Day Workflow: The Next Stage in a Sequencing Revolution
    With the ability to prepare up to 13 libraries in a little over 2 hours, the Ion Xpress™ Plus Fragment Library Kit for AB Library Builder™ System is a key step towards automation of the Ion sequencing workflow, making comprehensive analyses of your sample(s) of interest more convenient than ever before. Furthermore, Ion Xpress™ Plus fragment libraries generated using the AB Library Builder™ system exhibit the superb coverage uniformity typically seen with proprietary Ion Shear™ DNA fragmentation chemistry and higher recovery rates than other library construction methodologies. So you can be confident of generating the best data in the shortest time, without the hassle or expense of manual shearing and size selection.

    Ion Torrent Sequencing Made Simpler, Faster, and More Affordable
    Ion Shear™ Plus DNA fragmentation technology eliminates the need for costly physical shearing devices for most applications and requires as little as 50 ng of sample, accelerating your path to semiconductor sequencing. This flexible technology also provides users the ability to adjust fragmentation and size-selection sizes to accommodate a range of sequencing read lengths depending on their project requirements. This automated library preparation solution provides fast and scalable workflows for sequencing projects requiring low- to high-throughput processing capabilities.

    For Research Use Only. Not for human or animal therapeutic or diagnostic use.

    Ion AmpliSeq™ Comprehensive Cancer Panel Ion Torrent™

    The Ion AmpliSeq™ Comprehensive Cancer Panel provides highly multiplexed target selection of genes implicated in cancer research. Encompassing over 50% of the Wellcome Trust Sanger Institute Cancer Gene Census, this is the most comprehensive cancer gene panel available. With all-exon coverage of 409 genes, the Ion AmpliSeq™ Comprehensive Cancer Panel delivers fast, FFPE-compatible, target selection for a broad survey of key genes for semiconductor sequencing. View the Ion AmpliSeq™ Comprehensive Cancer Panel list of target genes (PDF).

    The Ion AmpliSeq™ technology allows ultra-high multiplex PCR combined with targeted sequencing library construction in just 16 hours for over 400 genes. Utilizing only 10 ng of input DNA per primer pool for a total of 40 ng of input DNA, analysis of restricted samples like FFPE samples is possible. The Ion AmpliSeq™ Comprehensive Cancer Panel is optimized for library construction with the Ion AmpliSeq™ Library Kit 2.0. Libraries are then ready for template preparation on the Ion OneTouch™ System and sequencing on the Ion PGM™ Sequencer. The Ion AmpliSeq™ Comprehensive Cancer Panel is not compatible with Ion Ampliseq™ 2.0 Beta Kits.

    Features and Benefits:

    • Broad survey of 409 key genes in a simple PCR reaction, no additional capital equipment required
    • Unmatched plexy of 16,000 primer pairs in only four pools with Ion AmpliSeq™ technology
    • Low DNA input of only 40 ng DNA and short amplicons enable FFPE samples and needle biopsies
    • Start comprehensive genomic studies quickly with pre-designed primer pools
    • Simplify analysis and annotation of variants with Ion Reporter™ software

    Comprehensive Gene Content Including Genes from Hotspot Panel
    Ion Torrent has designed the most extensive cancer panel available for sequencing with Ion PGM™ and, soon, Ion Proton™ Sequencers. Working with key cancer researchers and reviewing literature and databases, the Ion AmpliSeq™ Comprehensive Cancer Panel was designed to target all exons of key tumor suppressor genes and oncogenes most frequently cited and most frequently mutated. Strategically designed to interrogate CDS and splice variants across multiple gene families simultaneously, pathway-based gene selection profiles mutational spectrum in cancer driver genes and drug targets, along with signaling cascades, apoptosis, DNA repair, transcription regulators, inflammatory response, and growth factor genes in a single assay. Additionally, all genes from the focused Ion AmpliSeq™ Cancer Panel are included in the Ion AmpliSeq™ Comprehensive Cancer Panel providing corresponding complementary data.

    Unmatched Level of Multiplex PCR
    The Ion AmpliSeq™ Comprehensive Cancer Panel is comprised of four primer pools totaling almost 16,000 primer pairs covering 409 genes-that's approximately 4,000 primer pairs in each pool! Used in conjunction with the Ion AmpliSeq™ Library Kit 2.0, the Ion AmpliSeq™ Comprehensive Cancer Panel maintains high uniformity and specificity at this high plexy, advancing multiplex PCR to new levels.

    Over 400 Genes, Only 40 ng DNA Required
    While other target selection methods typically require micrograms of DNA input, the Ion AmpliSeq™ Comprehensive Cancer Panel uses only 40 ng DNA. This breakthrough in low DNA input requirement enables the interrogation of restricted samples like formalin-fixed, paraffin-embedded samples (FFPE) and fine needle aspiration biopsies (FNAB). Additionally, shorter amplicon design (average 155 bp) allows for compatibility with degraded samples.

    Simplified Target Selection Without Primer Design
    With pre-designed primers in the Ion AmpliSeq™ Comprehensive Cancer Panel, researchers can bypass gene selection, primer design, and optimization, and advance straight to generating results for a broad survey of hundreds of genes in key research samples. To further focus your cancer research, you may choose to conduct in-depth somatic variant analysis on a subset of genes or specific cancer subtype. Using Ion AmpliSeq™ Designer, researchers can simply add or subtract genes from this panel to create your own custom panel. The flexibility and scalability of Ion AmpliSeq™ Solutions spans across the Ion AmpliSeq™ Ready-to-use Panels and Ion AmpliSeq™ Custom Panels.

    For Research Use Only. Not for any animal or human therapeutic or diagnostic use.

    Iodine-Water-Pyridine-Tetrahydrofuran Oxidizer Solution (0.02 M) Applied Biosystems™

    This Iodine⁄Water⁄Pyridine⁄Tetrahydrofuran (oxidizer) solution comes in a convenient large volume for ABI 394 Nucleic Acid synthesizers, resulting in extended hands-free DNA synthesis. With these larger bottles attached your synthesizer can produce up to 40 average primer-length oligonucleotides with no bottle changes, reducing attended operation time by 50%.

    • Reagent concentrations are within our strict specifications, guaranteeing consistent quality.
    • Our performance specification of at least 98% stepwise coupling efficiency is assured, increasing oligonucleotide synthesis yields of full-length product.
    • Reagent kits are available for your convenience, and save you time and money.

    Our high-performance reagents begin with raw materials that must conform to strict specifications. Once the reagents are manufactured and packaged, we perform extensive testing to assure quality. Reagent lifetime on the instrument is two weeks for tetrazole, and six weeks for all other reagents.

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

    MethylMiner™ Methylated DNA Enrichment Kit Applied Biosystems™

    The MethylMiner™ Methylated DNA Enrichment Kit is for highly sensitive enrichment of methylated DNA for downstream analysis including PCR/qPCR based assays, bisuflite conversion followed by amplification, cloning, and sequencing, direct sequencing, library preparation for high-throughput sequencing, and sample-prep for DNA microarray analysis. Patterns of DNA methylation seem to be important for making determinations about development and diseases such as cancer. This kit enables superior enrichment and differential fractionation of double-stranded DNA based on CpG methylation density, with increased sensitivity over antibody-based methods. Fractionation permits important comparisons between samples and enables researchers to focus analysis on only the methylation densities of interest.
    • Partitioning with high affinity binding—at least 4-fold greater sensitivity than antibody-based methods
    • Fractionation based on CpG methylation density—ds DNA capture is achieved with MBD2 protein and facilitates ligation of double-stranded adaptors for next-generation sequencing
    • Rapid and easy elution with salt eliminates the need for proteinase K treatment and phenol:chloroform extraction
    • Precise answers—fractionated DNA permits distinctions to be made regarding methylation status and density
    • Fast protocol—completed in less than 4 hours
    • Easy—simple handling with Dynabeads® the gold standard magnetic beads

    Ion AmpliSeq™ Direct FFPE DNA Kit Ion Torrent™

    The Ion AmpliSeq™ Direct FFPE DNA Kit enables the preparation of DNA from formalin-fixed, paraffin-embedded (FFPE) tissues for library construction using the Ion AmpliSeq protocol, without the need for deparaffinization or DNA purification. This kit is suitable for FFPE tissue sections up to 10 µm thick.

    Features of the Ion AmpliSeq Direct FFPE DNA Kit include:
    • Simple one-tube 2-step protocol that minimizes sample loss
    • Efficient 30-minute workflow with only 10 minutes of hands-on time
    • Ideal for FFPE DNA samples with limited DNA amount
    • No deparaffinization of FFPE sections required
    • No column or bead-based DNA purification required
    • Ion AmpliSeq library preparation with as little as 1 ng input DNA
    • Uracil-D-glycosylase treatment to remove deaminated cytosines is an optional step

    Extraction of DNA from samples with limited DNA amount
    Archived tissue samples can provide clinically relevant information, but it can be difficult to isolate the small amount of nucleic acid they contain. Deparaffinization of FFPE tissue sections and purification of the DNA in these samples can be a complicated, multi-step procedure requiring considerable hands-on time, and the associated sample-loss makes it an unsuitable approach for processing FFPE DNA samples with limited DNA amounts.

    A simpler and faster method
    The Ion AmpliSeq Direct FFPE DNA Kit provides a user-friendly protocol that eliminates the need for deparaffinization of FFPE tissue sections and purification of the DNA. From an FFPE section mounted on a glass slide, the area of interest is removed using Transfer Solution and pipetted into a PCR tube or 96-well plate. After the addition of Direct Reagent, the sample is incubated at 65°C for 15 minutes. The FFPE DNA is now ready for the Ion AmpliSeq™ Library Preparation protocol. The prepared FFPE DNA can be quantified using the Qubit™ HS DNA Quantitation Kit, if necessary. The simplicity of this protocol eliminates the need for complicated deparaffinization and DNA extraction procedures, and libraries can be prepared either manually or with the automated Ion Chef™ System.

    Bulk CPG (Controlled Pore Glass), 500 Angstrom pore size, T Thermo Scientific™

    Bulk T Controlled Pore Glass (CPG) for users to pack their own columns for synthesis of oligonucleotides <50 bases in length.

    • Proprietary design and manufacturing methods ensure consistency and high quality
    • The 500 angstrom pore size of the support allows synthesis of oligonucleotides of up to 50 bases
    • Save time and money

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

    Trichloroacetic Acid Dichloromethane, Deblocking Solution Applied Biosystems™

    This is a four-pack of 450 mL Trichloroacetic acid (TCA)⁄Dichloromethane (DCM) solution.

    This trichloroacetic acid⁄dichloromethane solution comes in a convenient large volume for ABI 394 Nucleic Acid synthesizers, resulting in extended hands-free DNA synthesis. With these larger bottles attached your synthesizer can produce up to 40 average primer-length oligonucleotides with no bottle changes, reducing attended operation time by 50%.

    • Reagent concentrations are within our strict specifications, guaranteeing consistent quality.
    • Our performance specification of at least 98% stepwise coupling efficiency is assured, increasing oligonucleotide synthesis yields of full-length product.
    • Reagent kits are available for your convenience, and save you time and money.

    Our high-performance reagents begin with raw materials that must conform to strict specifications. Once the reagents are manufactured and packaged, we perform extensive testing to assure quality. Reagent lifetime on the instrument is two weeks for tetrazole, and six weeks for all other reagents.

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

    Collibri™ PS DNA Library Prep Kit for Illumina Systems, with UD indexes (Set A, 1-24) Invitrogen™

    The Invitrogen Collibri PS DNA Library Prep Kit prepares libraries for whole genome sequencing (WGS) on high-throughput Illumina next-generation sequencing (NGS) systems. The kit is suitable for physically sheared (PS) genomes of all sizes and variable quality, including FFPE samples.

    The Collibri PS DNA Library Prep Kit:
    • Includes in-process visual feedback at every step of the process to confirm proper mixing of reagents for the highest chance of library prep success
    • Includes all necessary components in a single kit
    • Offers consistent, even coverage of variable GC regions from inputs ranging from 1 to 1,000 ng
    • Offers improved coverage of challenging genomic regions compared to already available library prep technologies
    • Provides up to 96 combinatorial dual or unique dual indexes
    • Is applicable for automation of library preparation

    The Collibri PS DNA Library Prep Kit contains inert dyes that provide visual feedback during library preparation: the reaction mixes change color in response to the addition of critical components at each step. The inert dyes do not interfere with enzymatic reactions and do not compromise sequencing results.

    The Collibri PS DNA Library Prep Kit consistently offers higher confidence SNP and INDEL calls resulting from stronger coverage of challenging genomic regions from a wide range of inputs (1 ng to 1 µg) of physically sheared double-stranded DNA (see figure below). Additionally, a PCR-free version is offered for inputs starting at 500 ng DNA. The entire library preparation protocol takes about 3.5 hours with a PCR workflow. The kit contains adapters with unique dual indexes (UDIs) or combinatorial dual indexes (CDs) that allow pooling of up to 24 or 96 different samples before the sequencing run.

    Applications
    The Collibri PS DNA Library Prep Kit is recommended for:
    • Whole genome sequencing
    • Resequencing
    • de novo assembly

    GeneArt™ Gibson Assembly HiFi Cloning Kit, electrocompetent cells Invitrogen™

    The GeneArt Gibson Assembly HiFi Cloning Kit enables DNA assembly and cloning via a technique that allows multiple overlapping DNA fragments to be seamlessly linked in a one-step, 15–60 minute isothermal reaction. DNA fragments of different lengths are uniformly assembled using complementary overlaps between fragments. The inherent flexibility of this approach is suitable for small and large DNA constructs and includes both single and multiple inserts. The resulting products can be used for a variety of downstream applications including transformation, PCR and rolling circle amplification (RCA). The GeneArt Gibson Assembly HiFi Cloning Kit, electrocompetent cells, is a complete kit that includes master mix, positive control, water, and ElectroMAX DH10B electrocompetent E. coli.

    Features of the GeneArt Gibson Assembly HiFi Cloning Kit include:
    Simple—seamlessly assemble and clone up to six DNA fragments in a single reaction
    Efficient—high fidelity provides more correct clones than other methods
    Flexible—design guidelines allow assembly into any vector of your choice
    Convenient—available as master mix kits and cloning kits complete with chemical or electrocompetent cells
    Trusted—over 4000 citations in the scientific literature highlighting great success

    Seamless assembly of multiple fragments
    GeneArt Gibson Assembly HiFi cloning is a simple, one-step process whereby up to six fragments are combined in a proprietary enzymatic mix in order to assemble DNA fragments with shared terminal end homology without leaving any extra sequences or scars behind (seamless). After a 15–60 minute incubation, a portion of the assembly reaction is then transformed into chemically competent or electrocompetent cells, yielding clones that are ready for analysis the next day. The required 20- to 40-base pair end homology is designed into the de novo fragment for synthesis or can be easily engineered by PCR amplification with custom DNA oligos. This special enzyme mix creates a seamless and covalently bound DNA construct providing high efficiency.

    Robust method for maximum efficiency
    Due to the covalently bound final product, the GeneArt Gibson Assembly HiFi method allows the utilization of chemically competent cells or electrocompetent cells for the highest transformation efficiency, improving the success of finding the right clone, particularly for more challenging constructs. There is no need for restriction enzymes, ligation, or recombination sites, and the method provides a perfectly seamless construct without unwanted extra bases.

    Provides great versatility
    The GeneArt Gibson Assembly HiFi method provides versatility, can streamline many techniques through the rapid combination, addition, deletion, or exchange of DNA segments, and eliminates the need to subclone, saving time and effort in the cloning workflow.

    Convenient formats
    GeneArt Gibson Assembly HiFi kits are available in multiple formats, including:
    • GeneArt Gibson Assembly HiFi Cloning Kit, electrocompetent cells (with ElectroMAX DH10B electrocompetent cells) (this page)
    GeneArt Gibson Assembly HiFi Cloning Kit, chemically competent cells (with One Shot TOP10 chemically competent cells)
    GeneArt Gibson Assembly HiFi Master Mix kits (cloning kit without the cells)

    ONC ION AMPLISEQ FOR CHEF, DL8 Ion Torrent™

    This is a replicate of the existing AmpliSeq SKU A29024 for revenue under the CS4 PL to be bundled with Oncomine tumor specfic panels.

    dGTP BigDye™ Terminator v1.0 Ready Reaction Cycle Sequencing Kit Applied Biosystems™

    dGTP BigDye® Terminator Cycle Sequencing Kit with the AmpliTaq® DNA Polymerase, FS. This Ready Reaction Kit uses the same dye set as the BigDye® v1.0 kits.

    The dGTP BigDye® Terminator Cycle Sequencing Kit's fluorescent dideoxy terminator chemistry is optimized for sequencing through GT- and G-rich templates.

    • Ensure reliable results with difficult regions and finishing applications.
    • Sequence templates with challenging sequence contexts.
    • Sequence problematic templates that standard chemistries cannot.

    Sequence Challenging Templates
    The dGTP BigDye® Terminator Kit is ideal for working with GT- and G-rich and other difficult-to-sequence templates. The dGTP BigDye® Terminator Kit replaces dITP with dGTP and it enables you to extend through those difficult-to-sequence regions with confidence, avoiding early signal loss in these samples.

    Optimized for GT-Rich Templates
    Obtain higher success rate even with your difficult GT-rich templates. By using the same chemistries as the standard BigDye® Terminator Kits (only replacing dITP with dGTP) the dGTP BigDye® Terminator Kit provides proven performance, optimized for GT-rich and other difficult-to-sequence templates.

    Easily Integrate into Your Workflow
    dGTP BigDye® Terminator Kits require no new software or instrument recalibration, so you can easily integrate it into your current workflow with minimal changes to your protocols.

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

    Ion Universal Library Quantitation Kit Thermo Scientific™

    The Ion Universal Library Quantitation Kit is an easy-to-use, flexible solution for the accurate quantitation of library input generated by the Ion 16STM Metagenomics Kit for Ion Torrent™ semiconductor sequencing. This kit provides the TaqMan® assay, TaqMan® Universal Master Mix, and library standard needed to quantify femtomolar amounts of Ion fragment libraries. With cycling conditions that allow both fast and standard cycling, the Ion Universal Library Quantitation Kit supports most real-time platforms. This real-time PCR kit enables greater accuracy and specificity compared to non-PCR or non-probe-based methods, delivering simplicity and speed to the Ion PGM™ System sequencing workflow.

    The Ion Universal Library Quantitation Kit enables:
    • Precision—TaqMan® assays enable greater specificity and accuracy in detecting properly adapted, amplifiable templates over non-probe-based quantitation methods
    • Sensitivity—the protocol supports quantitation of femtomolar amounts of fragment libraries
    • Simplicity—the validated, ready-to-use qPCR standard requires only a simple serial dilution to determine the optimal concentration of library to use for templated bead preparation
    • Versatility—the highly robust qPCR mix accommodates a wide range of cycling conditions and reaction volumes, and combines highly sensitive detection with a broad quantification range
    • Efficiency—qPCR-based methods use less material for quantification

    This kit includes:
    • A TaqMan® assay designed for Ion library adaptors
    • TaqMan® Universal PCR Master Mix
    • An adapted E. coli DH10B library control of a defined size constructed using the Ion Fragment Library Kit to yield an adapted library ~190 bp in size

    Note: In addition to use with the Ion 16S™ Metagenomics Kit workflow, the Ion Universal Library Quantitation kit is also compatible with sequencing workflows for amplicons generated using any master mix.

    MicroSEQ™ ID Microbial Identification Software v3.0 Lite Applied Biosystems™

    MicroSEQ® ID Microbial Identification Software allows you to easily identify and classify unidentified bacterial or fungal sequences by comparing them to a validated microbial library. The Lite version of the software can be used on a stand-alone PC (not connected to the genetic analyzer) for simple analyses.

    • A validated library of over 2300 microbial sequences help ensure you get the answers you need
    • Automatically identify unknown specimens
    • Run plates on Applied Biosystems® 3500 Series Genetic Analyzers directly via the MicroSEQ® ID Software
    • MicroSEQ® system is a complete integrated solution, including security, audit, and e-signature features
    • Qualification and validation support

    Confidently Identify Microbes
    The MicroSEQ® system comprises bacterial libraries of 500 bp sequences and over 2300 validated entries--including extensive coverage of gram-negative nonfermenters, Bacillus, Coryneforms, Mycobacteria, and Staphylococcus. Another library containing more than 1100 entries is available for fungal identification. To help ensure accurate identification of the species of your sequences, we rigorously validate all library entries. And unlike other widely available databases, MicroSEQ® libraries contain only correctly identified organisms and quality-controlled sequences derived from type strains of preeminent culture collections. The libraries also support sequence polymorphisms, and include bacterial Category A biothreat agents.

    Automatically Identify Unknown Specimens
    Reviewing each specimen in a project file to make a manual identification call can be tedious and time consuming. The new Auto-ID feature in MicroSEQ® ID Software v3.0 uses a set of editable parameters to automatically identify unknown specimens. The results table is displayed in the report, and an editable comments field allows additional information or manual identifications to be entered into the same table.

    Run Plates on 3500/3500xL Instruments Directly via the MicroSEQ® ID Software
    Applied Biosystems® 3500 Series Genetic Analyzer users are now able to run plates on these instruments directly via the MicroSEQ® ID Software v3.0 user interface, without needing Autoanalysis Manager. A single software wizard enables you to set up projects, specimens, and plates; adjust the plate layout via drag and drop; start and monitor the run; and review results.

    The MicroSEQ® System: A Complete, Integrated Solution
    Streamlining every step in microbial identification, the Applied Biosystems® MicroSEQ® system combines the advantages of MicroSEQ® ID Software with easy to use PrepMan® Ultra sample preparation reagents and protocols, MicroSEQ® bacterial and fungal application kits, and industry-leading thermal cyclers and sequencing systems. To help ensure optimal performance and system-wide integration, we develop and test all components of the system together. The MicroSEQ® ID Software also includes security, audit, and electronic signature features enabling the software to smoothly integrate into your workflow.

    Qualification and Validation Support
    To help ensure seamless integration into your laboratory, from installation to routine operation, we offer comprehensive installation and operational qualification (IQ/OQ) and validation support services.

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