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Service Details:
| ICMR Approved | Yes |
| Sample Type | Nasal and Throat Swabs |
| Brand | Illumina |
| Usage/Application | Laboratory |
| Packaging Type | Box |
| List no. | R |
Illumina provides a comprehensive suite of in vitro diagnostic (IVD) kits designed to support clinical laboratories in delivering accurate, efficient, and reliable next-generation sequencing (NGS)–based diagnostics. These kits include library preparation reagents, sequencing consumables, and complete assay solutions, all developed under strict regulatory standards including FDA regulation and CE-IVD marking.
Key Features:
• Regulatory Compliance: FDA-regulated and CE-IVD marked, ensuring suitability for clinical diagnostics.
• Instrument Compatibility: Works seamlessly with multiple Illumina Dx instruments.
• Streamlined Workflows: Supports automated library preparation and analysis for efficient laboratory operations.
• Clinical Applications: Assay kits available for oncology, non-invasive prenatal testing (NIPT), hereditary disorders, and other diagnostic applications.
• High Reliability: Ensures reproducible results with minimal hands-on time and robust quality control.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Sample Type | Nasal and Throat Swabs |
| Brand | illumina |
| ICMR Approved | Yes |
| Usage/Application | Laboratory |
| Packaging Type | box |
| list no. | R |
The Illumina TruSight Oncology 500 Selection Tool is an interactive online resource designed to help laboratories identify the most suitable TruSight Oncology 500 assay based on sample type, sequencing platform, automation capabilities, and research goals. By entering parameters such as tissue or liquid biopsy samples, desired throughput, and available instrumentation, users receive tailored assay recommendations for efficient comprehensive genomic profiling (CGP) in oncology studies. This tool streamlines workflow decisions, ensuring optimized and effective clinical research outcomes.
Key Features:
• Customized Assay Recommendations: Provides assay suggestions based on sample type, throughput needs, and sequencing platform compatibility.
• Supports Diverse Sample Types: Compatible with formalin-fixed paraffin-embedded (FFPE) tissue and circulating tumor DNA (ctDNA) from liquid biopsies.
• Integration with Sequencing Platforms: Aligns with Illumina NextSeq and NovaSeq systems for seamless workflow integration.
• Optimized for Automation: Identifies assays compatible with automated library preparation systems, reducing hands-on time and enhancing scalability.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with the listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Sample Type | Nasal and Throat Swabs |
| Brand | Illumina |
| ICMR Approved | Yes |
| Usage/Application | Laboratory |
| Packaging Type | Box |
| List no. | R |
The Illumina Library Prep and Array Kit Selector is an intuitive, web-based tool designed to help researchers quickly identify the most suitable sequencing library preparation kits or microarrays for their projects, including immuno-oncology research. By applying filters such as research area, application method, species, and system compatibility, users can efficiently narrow down options to select kits that precisely match their experimental needs. This tool streamlines workflows, enabling researchers to compare, share, and order kits with ease.
Key Features:
• Customized Filtering: Apply filters based on research area, application method, species, and system for highly relevant results.
• Comprehensive Results: Access a broad range of library prep kits and microarrays tailored to immuno-oncology research.
• User-Friendly Interface: Easily compare, share, and order kits directly through the platform.
• Research-Focused: Facilitates studies in immuno-oncology and related research areas.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For actual pricing and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Machine Condition | New |
| Imaging Mode | 3D/4D |
| Usage/Application | Laboratory instrument |
| Model Name/Number | Illumina MiSeqDx Instrument |
| Brand | illumina |
| Clinical Application | Cardiac Imaging |
| Connectivity Ports | 2 |
| list no. | R |
The Illumina MiSeqDx Instrument is the first FDA-regulated and CE-IVD–marked next-generation sequencing (NGS) platform purpose-built for clinical laboratories. Leveraging Illumina's proven sequencing by synthesis (SBS) technology, it delivers highly accurate and reliable results for targeted DNA sequencing applications. With dual operating modes—IVD for clinical diagnostics and RUO (Research Use Only) for assay development—the MiSeqDx provides unmatched flexibility for both diagnostic testing and research workflows.
Key Features:
• Regulatory Compliance: FDA-regulated and CE-IVD–marked, ensuring suitability for clinical diagnostic applications.
• Flexible Operation Modes: Switch seamlessly between IVD and RUO modes to meet diverse laboratory needs.
• Integrated Software: User-friendly touchscreen interface simplifies run setup, sample tracking, and data analysis.
• High-Quality Data Output: Generates ≥5 Gb per run, ≥15 million paired-end reads, with ≥80% of bases achieving Q30 quality scores for reliable sequencing results.
• Targeted DNA Sequencing: Ideal for clinical applications such as genetic testing, oncology research, and personalized medicine.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and/or logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.
Service Details:
| Model Name/Number | Viper LT |
| Automation | Fully Automatic |
| User Input | Touch |
| Display | Digital |
| Depth | 70 |
| Width | 90 |
| Height | 60 |
| Time To First Result | 1.5-3 hours |
| Weight | 90 kg |
| Voltage | 100-240 V AC, 50-60 Hz |
| Brand | Becton |
| List No | R |
The BD Viper LT System is a compact, fully automated molecular diagnostic platform designed for high-throughput testing of sexually transmitted infections (STIs) and human papillomavirus (HPV). It integrates nucleic acid extraction, amplification, and detection into a single tabletop instrument, streamlining laboratory workflows and reducing hands-on time.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Key Features:
Automated nucleic acid extraction and amplification with minimal user intervention.
Supports a variety of assays, including BD ProbeTec CT/GC and BD Onclarity HPV Assay.
Room temperature storage of reagents and unit-dose formats to minimize waste.
Bi-directional Laboratory Information System (LIS) integration for seamless data management.
Service Details:
| Instrument Name | IVDs & Analyzers |
| Model Name/Number | NextSeq 550Dx |
| Usage/Application | Clinical |
| Brand | Illumina |
| Automation | Semi Automatic |
| User Input | Touch |
| Display | Digital |
| Storage | Network storage support |
| List no. | R |
Dual-mode: IVD and Research Use (RUO)
Up to 120 Gb output per run, 2×150 bp reads
Sequencing-by-Synthesis (SBS) with 2-channel detection
Integrated Local Run Manager and DRAGEN compatibility
FDA-cleared and CE-IVD marked for clinical applications
Service Details:
| Number of preps | 10 |
| ICMR Approved | Yes |
| Sample Type | Oral and Nasal Swab |
| Brand | Illumina |
| Packagint Type | Box |
| Packaging Type | Box |
| LIST NO. | R |
The Illumina Library Prep and Array Kit Selector is an intuitive, research-focused tool that helps scientists identify the most suitable sequencing library preparation kits or microarrays for their specific projects, including cancer research studies. By applying filters such as research area, application method, species, and system compatibility, users can efficiently narrow down options to find kits that align with their experimental requirements. This tool streamlines selection, enabling researchers to compare, share, and order the most appropriate kits for their studies.
Key Features:
Customized Filtering: Apply filters based on research area, application method, species, and system to quickly identify relevant kits.
Comprehensive Results: Access a broad range of library prep kits and microarrays tailored for cancer and other research areas.
User-Friendly Interface: Easily compare, share, and order kits directly through the platform.
Research-Focused Design: Facilitates efficient study planning for cancer and related research projects.
Note:
The price mentioned above is for reference only; do not consider it for purchase. For actual price and more product details, please contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer:
Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and/or logos (collectively called “marks”) associated with the products are used solely for identification purposes and belong to their respective owners. No association with the mark owners is claimed unless explicitly stated. Meaning of List Codes: R – Refurbished | PO – Pre-Owned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| ICMR Approved | Yes |
| Brand | Illumina |
| Packagint Type | Box |
| Sample Type | Oral & Nasal Swab |
| Packaging Type | box |
| list no. | R |
The Illumina Library Prep and Array Kit Selector is an intuitive, web-based tool designed to help researchers quickly identify the most suitable sequencing library preparation kits or microarrays for their projects, including immuno-oncology research. By applying filters such as research area, application method, species, and system compatibility, users can efficiently narrow down options to select kits that precisely match their experimental needs. This tool streamlines workflows, enabling researchers to compare, share, and order kits with ease.
Key Features:
• Customized Filtering: Apply filters based on research area, application method, species, and system for highly relevant results.
• Comprehensive Results: Access a broad range of library prep kits and microarrays tailored to immuno-oncology research.
• User-Friendly Interface: Easily compare, share, and order kits directly through the platform.
• Research-Focused: Facilitates studies in immuno-oncology and related research areas.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For actual pricing and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| ICMR Approved | Yes |
| Usage/Applications | Laboratory |
| Packaging Type | Box |
| Brand | Illumina |
| Sample Type | Oral swabs |
| List No. | R |
The Illumina Library Prep and Array Kit Selector is an interactive online tool designed to help researchers identify the most suitable sequencing library preparation kits and microarrays for their specific projects, including studies in complex disease genomics. By using customizable filters such as research area, application method, species, and system compatibility, users can quickly narrow down options to find kits that match their experimental requirements. This tool streamlines the library selection process, enabling researchers to efficiently compare, share, and order kits tailored to their study needs.
Key Features:
• Customized Filtering: Apply filters by research area, application method, species, and system to find relevant kits.
• Comprehensive Results: Access a wide range of library prep kits and microarrays suitable for complex disease genomics.
• User-Friendly Interface: Easily compare, share, and order kits directly through the platform.
• Research-Focused: Designed specifically for research applications in genomics and molecular biology.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Number of preps | 10 |
| Brand | Illumina |
| ICMR Approved | Yes |
| Shelf Life | 12 Months |
| Type | Manual |
| List no. | R |
The Illumina Library Prep and Array Kit Selector is an interactive tool designed to assist researchers in selecting the most appropriate sequencing library preparation kits or microarrays for their specific agrigenomics projects. By applying filters such as area of research, application method, species, and system compatibility, users can efficiently identify kits that align with their experimental needs. This tool streamlines the selection process, ensuring that researchers can compare, share, and order kits that best fit their study requirements.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Key Features:
Customized Filtering: Apply filters based on research area, application method, species, and system to find relevant kits.
Comprehensive Results: Access a broad range of library prep kits and microarrays tailored to agrigenomics research.
User-Friendly Interface: Easily compare, share, and order kits directly through the platform.
Research-Focused: Designed specifically for research use, facilitating studies in agrigenomics and related areas.
Service Details:
| Service Includes | Library Design |
| ICMR Approved | Yes |
| Brand | Illumina |
| Packaging Type | Box |
| Usage/Applications | Laboratory |
| List no. | R |
The Illumina Library Prep and Array Kit Selector is an interactive online tool designed to help researchers quickly identify the most suitable library preparation kits and microarrays for their specific applications, including drug discovery and development. By applying filters such as application type, method, species, and compatible systems, users can efficiently narrow down options, ensuring the selected kits and arrays align with experimental requirements. This tool streamlines workflow planning and supports efficient execution of genomic studies.
Key Features:
• Comprehensive Filtering: Select products based on application, method, species, and system compatibility.
• Tailored Recommendations: Get personalized suggestions for kits and arrays aligned with research needs in drug discovery.
• Integration with Illumina Platforms: Ensures full compatibility with a range of Illumina sequencing and microarray systems.
• Streamlined Workflow Planning: Facilitates efficient experiment setup by identifying the most appropriate kits and arrays.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| ICMR Approved | Yes |
| Sample Type | Nasal and Throat Swabs |
| Brand | Illumina |
| Usage/Application | Laboratory |
| Packaging Type | Box |
| list no. | R |
Illumina offers a comprehensive suite of microarray kits tailored for genotyping and epigenetic analysis, enabling researchers to explore genetic variations and DNA methylation patterns across various species and study designs. These kits are designed for high-throughput applications and are compatible with Illumina platforms like the iScan and NextSeq 550 systems.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
High Throughput: Capable of processing thousands of samples per week, suitable for large-scale studies.
Single-Nucleotide Resolution: Provides precise measurements for both genotyping and methylation analyses.
Automation Compatibility: Supports integration with automated systems to enhance workflow efficiency.
Customizable Content: Offers options for custom array designs to meet specific research needs.
Service Details:
| Usage/Application | Lab |
| Capacity | 8 Sample Plates |
| Read Length | 200-400 bp |
| Model Name/Number | MiSeq System |
| Amplification Approach | PCR |
| Color | White |
| Time Per Run | 5.5 hours |
| Brand | Illumina |
| Run time | 4-56 hr |
| list no. | R |
The Illumina MiSeq System is a high-performance benchtop next-generation sequencing (NGS) platform designed for rapid, cost-effective DNA and RNA sequencing. It supports a wide array of applications, including targeted gene sequencing, small genome sequencing, amplicon sequencing, 16S metagenomics, and gene expression profiling. With adjustable read lengths and short run times, the MiSeq delivers high-quality sequencing results suitable for both research and clinical laboratories.
Key Features:
• Flexible Output: Generates 540 Mb to 15 Gb per run, accommodating small to medium-scale projects.
• Variable Read Lengths: Supports reads up to 2 × 300 bp for high-resolution sequencing.
• Rapid Run Time: Runs range from approximately 4 to 56 hours, depending on read length and application.
• Software Integration: Includes MiSeq Reporter for secondary data analysis and access to BaseSpace Sequence Hub for cloud-based data management.
• Versatile Applications: Ideal for genomic research, microbiome analysis, precision medicine, and translational studies.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Capacity | 16 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 700 bp |
| Sample Volume | 18537 |
| Throughput | 576 |
| Sequencing Chemistry | Pyrosequencing |
| Data Output Per Run | 100-200 mb |
| list no. | R |
The Illumina NextSeq 1000 and NextSeq 2000 Sequencing Systems are advanced benchtop next-generation sequencing (NGS) platforms designed for high-throughput, flexible, and cost-effective sequencing across a wide range of laboratory applications. Utilizing Illumina’s XLEAP-SBS chemistry and patterned flow cell technology, these systems deliver enhanced data quality, scalability, and reliability. The NextSeq 1000 is optimized for laboratories requiring moderate throughput, while the NextSeq 2000 supports high-throughput applications, accommodating larger studies and complex workflows.
Key Features:
• XLEAP-SBS Chemistry: Advanced sequencing-by-synthesis technology ensures faster, more robust, and high-quality sequencing results.
• Patterned Flow Cells: Nanowell-patterned flow cells increase cluster density and sequencing output, enhancing data accuracy and consistency.
• Integrated DRAGEN Analysis: Onboard DRAGEN Bio-IT platform provides accelerated and accurate secondary data analysis, reducing turnaround time.
• Flexible Throughput Options: Multiple flow cell configurations (P1–P4) support varying throughput needs, with the NextSeq 2000 delivering up to 1.8 billion single-end reads per run.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For actual pricing and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Usage/Application | Laboratory |
| Model Name/Number | The NovaSeq 6000 |
| Color | White |
| Program Capacity | 8 sample plates |
| Brand | Illumina |
| Capiliaries | 96 |
| list no. | R |
The Illumina NovaSeq 6000 System is a high-throughput next-generation sequencing (NGS) platform designed for large-scale genomic studies. Utilizing advanced sequencing by synthesis (SBS) chemistry and patterned flow cell technology, it delivers exceptional scalability, flexibility, and data accuracy. With tunable output options and customizable flow cell configurations, the NovaSeq 6000 supports a wide range of applications, including whole-genome sequencing, exome sequencing, transcriptomics, and complex genomic analyses, enabling researchers to gain comprehensive genomic insights efficiently.
Key Features:
• Scalable Throughput: Generates up to 6 Tb of data and 20 billion reads per run, supporting projects of all sizes.
• Flexible Flow Cell Configurations: SP, S1, S2, and S4 flow cells allow optimization based on project throughput and application.
• Advanced SBS Technology: Ensures high accuracy and reliable sequencing with Illumina’s proven chemistry.
• Integrated Data Analysis: Compatible with DRAGEN Bio-IT Platform and BaseSpace Sequence Hub for streamlined data processing and interpretation.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Capacity | 8 sample plates |
| Brand | Illumina |
| Color | White |
| Model Name | The NovaSeq X |
| Application | Laboratory |
| List No. | R |
The Illumina NovaSeq X Series, including the NovaSeq X and NovaSeq X Plus, represents a breakthrough in high-throughput next-generation sequencing (NGS). Designed for large-scale genomic studies, these systems deliver exceptional scalability, with the NovaSeq X Plus producing up to 16 terabases per run and the NovaSeq X up to 8 terabases per run. Featuring XLEAP-SBS chemistry and ultra-high-density patterned flow cells, the NovaSeq X Series ensures accurate, high-quality data and rapid sequencing performance.
Key Features:
• Ultra-High Throughput: Achieve up to 16 terabases per run on NovaSeq X Plus, enabling extensive genomic analyses.
• Advanced Chemistry: XLEAP-SBS chemistry for faster incorporation times and superior data quality.
• Integrated Analysis: Onboard DRAGEN secondary analysis accelerates data processing and reduces storage needs.
• Sustainable Design: Uses lyophilized reagents and minimized packaging for environmentally responsible operation.
Note: The price mentioned above is for reference only. For actual pricing and product details, please contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Brand | Illumina |
| Weight | 65 |
| Country of Origin | Made in India |
| Usage/Application | Labrotory |
| List No. | R |
The Illumina iScan System is a laser-based, high-resolution microarray scanner engineered for rapid, sensitive, and accurate imaging of Illumina BeadChips. Ideal for a wide range of genomic applications—including genotyping, DNA methylation analysis, and copy number variation (CNV) studies—the iScan System supports high-throughput sample processing with optional automation, enabling efficient workflows in complex disease genomics, molecular biology, and translational research.
Key Features:
• High Throughput: Scans up to 5,670 samples per week for large-scale genomic studies.
• Rapid Scan Times: Average scan time of 1.25 minutes per sample, enhancing laboratory efficiency.
• Exceptional Data Quality: Achieves high call rates (>99%) with sensitive measurements across a broad dynamic range.
• Automation Compatibility: Integrates with AutoLoader 2.x and liquid-handling robotics for 24/7 operation.
• Versatile Applications: Supports genotyping, DNA methylation profiling, CNV detection, and other advanced genomic analyses.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Capacity | 16 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 200-400 bp |
| Sample Volume | 43250 |
| Throughput | 384 |
| Amplification Approach | PCR |
| List No. | R |
| Brand | Illumina |
The Illumina NextSeq 550 System is a versatile benchtop next-generation sequencing (NGS) platform designed for laboratory use, integrating both sequencing and microarray scanning capabilities. It supports a broad range of applications, including whole-exome sequencing, transcriptome analysis, targeted panels, and genotyping, making it suitable for both research and clinical laboratories. With tunable output and rapid turnaround times, the NextSeq 550 enables efficient and scalable genomic studies.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Key Features:
Flexible Output: Offers up to 120 Gb of data per run with 2 × 150 bp read lengths, accommodating various throughput needs.
Integrated Microarray Scanning: Combines NGS and array technologies, allowing for expanded application versatility within a single instrument.
Rapid Turnaround: Delivers sequencing results in approximately 12 to 30 hours, depending on the application and read length.
User-Friendly Workflow: Features an intuitive interface with pre-filled reagent cartridges, streamlining the sequencing process.
Additional Information:
Service Details:
| Capacity | 8 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 200-400 bp |
| Sample Volume | 18537 |
| Sequencing Chemistry | Pyrosequencing |
| Amplification Approach | PCR |
| Time Per Run | 20 minutes-3 hours |
| Format | 384 well |
| List No. | R |
| Brand | illumina |
The Illumina MiSeq System is a compact, benchtop next-generation sequencing (NGS) platform designed for rapid, high-quality sequencing of DNA and RNA. Leveraging Illumina’s Sequencing by Synthesis (SBS) chemistry, it delivers accurate and reliable results across a wide range of applications, including targeted sequencing, small genome sequencing, amplicon sequencing, and 16S metagenomics. With its user-friendly interface and integrated data analysis tools, the MiSeq System is ideal for both research and clinical laboratories seeking efficient and cost-effective sequencing solutions.
Key Features:
• Versatile Applications: Supports targeted gene panels, small genomes, amplicons, and metagenomic studies.
• Rapid Turnaround: Produces results in as little as 4 hours, enabling fast data-driven decision-making.
• High Data Output: Generates up to 15 Gb per run with 2 × 300 bp paired-end reads for high-resolution sequencing.
• Integrated Data Analysis: Onboard tools plus BaseSpace Sequence Hub access for seamless data processing and sharing.
Note: The price mentioned above is for reference only. For actual pricing and product details, please contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, content on this website is the proprietary property of its owners. Trademarks, service marks, and logos are for identification purposes only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Instrument Name | IVD assay |
| Model Name/Number | Nextseq DX 550 System |
| Usage/Application | Laboratory |
| Brand | Illumina |
| Automation | Fully Automatic |
| User Input | Touch |
| Display | Digital |
| LIST NO. | R |
The Illumina NextSeq 550Dx System is a dual-mode, mid-throughput next-generation sequencing (NGS) platform designed for both in vitro diagnostic (IVD) applications and clinical research. It combines regulatory compliance with flexibility, enabling laboratories to perform IVD testing and develop laboratory-developed tests (LDTs) on a single instrument. With its integrated sequencing and microarray scanning capabilities, the system supports a wide range of applications, including oncology, reproductive health, and genetic disease research.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Key Features:
Dual Operating Modes: Offers both Diagnostic Mode for IVD testing and Research Mode for clinical research applications, providing versatility in a single platform.
High Data Output: Generates up to 120 Gb of data per run with paired-end reads of 2 × 150 bp, accommodating various throughput needs.
Regulatory Compliance: Meets global regulatory standards, including FDA and IVDR regulations, and is developed under design control principles with cGMP manufacturing.
Integrated Workflow: Features a simplified three-step workflow with onboard analysis software, facilitating efficient and accurate sequencing processes.
Service Details:
| ICMR Approved | Yes |
| Sample Type | Nasal and Throat Swabs |
| Brand | Illumina |
| Usage/Application | Laboratory |
| Packaging Type | Box |
| List no. | R |
Illumina offers a comprehensive suite of library preparation kits designed for a wide range of next-generation sequencing (NGS) applications, supporting diverse sample types, input amounts, and research goals. Optimized for Illumina sequencing platforms, these kits deliver high-quality, reproducible results across genomic, transcriptomic, and epigenomic studies. Whether handling low-input DNA, challenging samples, or specialized applications such as single-cell or targeted sequencing, Illumina provides reliable solutions tailored to your laboratory’s needs.
Key Features:
• Versatile Applications: Supports whole-genome sequencing, targeted sequencing, RNA-Seq, ChIP-Seq, and single-cell sequencing.
• Flexible Input Requirements: Compatible with various sample types and input quantities, from low-input DNA/RNA to FFPE tissues.
• Streamlined Workflows: Enables rapid library preparation, with some kits completing the process in as little as 90 minutes.
• Automation Compatibility: Supports automation platforms for high-throughput processing, reducing manual effort and improving reproducibility.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, or logos (“marks”) associated with the products listed here are for identification purposes only. No association with the mark owners is claimed unless explicitly specified. Meaning of List Codes: R – Refurbished | PO – Pre-Owned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| ICMR Approved | Yes |
| Packagint Type | Box |
| Brand | Illumina |
| Sample Type | Oral & Nasal Swab |
| Packaging Type | Box |
| Model Name | Reagents Kits for every Illumina |
| List no | R |
Illumina offers a comprehensive range of sequencing reagent kits designed specifically for its iSeq, MiSeq, NextSeq, and NovaSeq platforms, ensuring optimal performance and reliable results across diverse applications. These kits include ready-to-use cartridges and flow cells, tailored to throughput requirements from low to ultra-high, and leverage proven sequencing by synthesis (SBS) chemistry for high-quality, reproducible sequencing data. Ideal for applications ranging from targeted gene panels to whole-genome sequencing, these kits streamline workflows and minimize hands-on time.
Key Features:
• Platform-Specific Kits: Available for iSeq, MiSeq, NextSeq, and NovaSeq systems.
• Comprehensive Reagents: Includes everything needed for library preparation, cluster generation, and sequencing.
• Versatile Applications: Supports projects from targeted sequencing to whole-genome studies.
• Reliable Data Quality: Ensures high-accuracy sequencing with minimal hands-on effort.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Instrument Name | Sequencing Instrument |
| Model Name/Number | NovaSeq 6000Dx |
| Usage/Application | Laboratory |
| Brand | Illumina |
| Automation | Fully Automatic |
| User Input | Touch |
| Display | Digital |
| list no. | R |
The Illumina NovaSeq 6000Dx is a high-performance, versatile sequencing platform designed for clinical diagnostics and research applications. Featuring dual operating modes, it supports both IVD-compliant workflows and research-use only (RUO) studies, delivering scalable throughput and rapid sequencing for whole-genome, exome, and transcriptome analysis.
Key Features:
• Dual-Mode Operation: Supports IVD-compliant and RUO workflows for clinical and research flexibility.
• Ultra-High Throughput: Delivers up to 6 Tb of data and 20 billion reads per run.
• Regulatory Compliance: CE-IVD marked and FDA-registered for clinical diagnostic applications.
• Broad Application Support: Ideal for whole-genome sequencing (WGS), whole-exome sequencing (WES), oncology panels, and transcriptome studies.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with the listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Capacity | 16 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 700 bp |
| Sample Volume | 18537 |
| Throughput | 576 |
| Sequencing Chemistry | Pyrosequencing |
| Time Per Run | 2-4 hours |
| Data Output Per Run | 100-200 mb |
| Format | 384 well |
| List No. | R |
| Brand | illumina |
The Illumina HiSeq 3000 and HiSeq 4000 sequencing systems are high-throughput NGS platforms designed for large-scale genomic studies. Leveraging patterned flow cell technology and Illumina’s sequencing by synthesis (SBS) chemistry, these systems deliver accurate, efficient, and scalable sequencing results. The HiSeq 3000 employs a single flow cell, while the HiSeq 4000 features dual flow cells, enabling higher throughput for extensive research projects.
Key Features:
• HiSeq 3000: Single flow cell system with up to 750 Gb output per run.
• HiSeq 4000: Dual flow cell system delivering up to 1.5 Tb output per run.
• Patterned Flow Cells: Enhance cluster density and sequencing efficiency.
• Dual Surface Imaging: Improves data quality and read accuracy, ensuring reliable results.
Note: The price mentioned above is for reference only. For actual pricing and product details, please contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Capacity | 16 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 700 bp |
| Sample Volume | 18537 |
| Throughput | 576 |
| Sequencing Chemistry | Pyrosequencing |
| Data Output Per Run | 100-200 mb |
| List No. | R |
| Brand | illumina |
The Illumina HiSeq X Series, including the HiSeq X Five and HiSeq X Ten systems, was engineered for population-scale, ultra-high-throughput whole-genome sequencing. Leveraging patterned flow cell technology and advanced optics, these platforms were capable of generating up to 1.8 terabases of data per run, allowing the sequencing of tens of thousands of human genomes annually. While the HiSeq X Series has been discontinued as of April 2024, it revolutionized genomic research by dramatically lowering the cost per genome sequenced.
Key Features:
• Ultra-High Throughput: Generate up to 1.8 terabases per run, sequencing 8–16 human genomes at 30x coverage in under three days.
• Patterned Flow Cell Technology: Billions of nanowells at fixed locations ensure high cluster density, uniform feature size, and enhanced data quality.
• Cost-Effective Genomics: Enables whole-genome sequencing for less than $1,000 per genome, including instrument depreciation, consumables, library prep, and labor.
• Scalable Configuration: Expand the HiSeq X Five system to a HiSeq X Ten setup to meet increasing throughput demands.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos associated with listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Capacity | 8 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 700 bp |
| Sample Volume | 43250 |
| List No. | R |
| Brand | Illumina |
The Illumina MiniSeq System is a compact, benchtop next-generation sequencing (NGS) platform designed for targeted DNA and RNA sequencing applications. It provides an easy-to-use workflow ideal for research and clinical laboratories with low-to-mid throughput requirements. With streamlined library preparation and intuitive software, it delivers high-quality sequencing results with minimal hands-on time.
Key Features:
• High Output: Delivers up to 7.5 Gb of data and 25 million reads per run.
• Versatile Applications: Supports small genomes, targeted panels, and gene expression studies.
• Compact Design: Fits perfectly in space-constrained labs.
• Integrated Data Analysis: Onboard software with a user-friendly interface simplifies analysis and reporting.
Note: The price mentioned above is for reference only. For actual pricing and product details, contact us at +91 84461 74263 or +91 98508 70860.
Disclaimer: Unless otherwise indicated, the content of this website is the proprietary property of its owners. Trademarks, service marks, and logos (“marks”) associated with the listed products are for identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Additional Information:
Service Details:
| Usage/Application | Lab |
| Model Name/Number | Illumina iSeq 100 |
| Color | White |
| Brand | Illumina |
| Run time | 9.5-19 hr |
| List no. | R |
The Illumina iSeq 100 Sequencing System is a compact, entry-level next-generation sequencing (NGS) platform designed for high-quality DNA and RNA sequencing with a minimal footprint. Utilizing Illumina's sequencing by synthesis (SBS) technology, it delivers accurate and reliable results for a variety of applications, including small genome sequencing, targeted gene expression profiling, and 16S metagenomics. Optimized for rapid turnaround times and cost-effective sequencing, the iSeq 100 is ideal for laboratories looking to integrate NGS capabilities without significant infrastructure investment.
Key Features:
• Compact Design: Measures 30.5 cm × 33 cm × 42.5 cm and weighs 16 kg, fitting easily into standard lab spaces.
• Fast Run Times: Sequencing runs as short as 9.5 hours depending on read length and application.
• High Data Quality: Delivers over 80% of bases with a Q30 score for high-accuracy sequencing results.
• Versatile Applications: Supports small genome sequencing, targeted gene expression profiling, and 16S metagenomics.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For actual pricing and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number:R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer
Service Details:
| Number of Stages | Two-Stage Alarms |
| Type | Wireless |
| Usage/Application | Commercial |
| Brand | Illumina |
| Model Name/Number | Illumina iScan System |
| Remote Control | Yes |
| List no. | R |
The Illumina iScan High-Throughput Microarray Scanner is a laser-based, high-resolution microarray scanner designed for rapid, sensitive, and accurate imaging of Illumina BeadChips. Ideal for genotyping, DNA methylation analysis, and copy number variation (CNV) studies, the iScan System supports high-throughput sample processing with automation options, making it suitable for research in complex disease genomics, molecular biology, and translational research.
Key Features:
• High Throughput: Scans up to 5,670 samples per week, enabling large-scale genomic studies.
• Rapid Scan Times: Average of 1.25 minutes per sample for efficient workflow.
• Exceptional Data Quality: Achieves high call rates (>99%) with sensitive measurements across a broad dynamic range.
• Automation Compatibility: Integrates with AutoLoader 2.x and liquid-handling robotics for continuous 24/7 operation.
• Versatile Applications: Supports genotyping, CNV detection, DNA methylation profiling, and other advanced genomic analyses.
Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860.
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified. Meaning of List Number: R – Refurbished | PO – Preowned | U – Used | T – Trading | M – Own Manufactured | AD – Authorized Dealer of Original Equipment Manufacturer