Product Details:
| Minimum Order Quantity | 5 Piece |
| Brand | Illumina |
| Material | Stainless Steel |
| Phase | Single Phase |
| Resolution | High-resolution scanning (up to 3 um/pixel) |
| Speed | Rapid scanning for high-throughput workflows |
| Compatibility | Works with various microarray types |
| Integration | Seamlessly integrates with Illumina platforms |
| List No | R |
The Illumina I-Scan System is a high-resolution microarray scanner designed for advanced laboratory research. Built to deliver speed, accuracy, and data quality, the I-Scan system is optimized for use with Illumina’s BeadChips, enabling a wide range of genomic applications such as genotyping, methylation analysis, and cytogenetics. It offers seamless integration with Illumina’s GenomeStudio software, ensuring efficient data acquisition, analysis, and storage, making it ideal for high-throughput environments and precision research workflows.
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High-resolution laser scanner for Illumina BeadChips
Supports a broad range of applications: genotyping, methylation, CNV, gene expression
Fast scanning speed and high data throughput
Integrated with GenomeStudio software for streamlined analysis
Compact benchtop design with minimal footprint
High image quality with low background noise
Easy-to-use interface with minimal training required
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Product Details:
| Minimum Order Quantity | 5 Piece |
| Material | SS |
| Voltage | 230 V |
| Usage/Application | Laboratory |
| Capacity | 16 Sample Plates |
| Number Of Capillaries | 96 Capillaries |
| Capillary Length | 50 cm |
| Read Length | 200-400 bp |
| Sample Volume | 43250 |
| Throughput | 384 |
| Amplification Approach | PCR |
| List No | R |
The Illumina NextSeq 550 System is a versatile, high-throughput sequencing platform designed for both research and clinical applications. Combining robust performance with ease of use, the NextSeq 550 offers scalable throughput for whole-genome, transcriptome, and targeted sequencing. It also features cytogenomic array scanning capabilities, allowing researchers to integrate sequencing and array-based workflows on a single system. Ideal for labs needing flexibility and fast turnaround, the NextSeq 550 delivers accurate results across a wide range of genomic applications.
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 98508 70860, +91 84461 74263
Supports a wide range of sequencing applications: WGS, RNA-seq, targeted panels, and exomes
Mid- and high-output flow cell options for flexible throughput
Integrated microarray scanning capability
Simple, intuitive interface with onboard data analysis tools
Broad compatibility with Illumina’s sequencing reagent kits
Output up to 120 Gb per run with high data quality
Ideal for clinical research, oncology, microbiology, and reproductive health
UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified.MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
| Minimum Order Quantity | 5 Piece |
| Usage/Application | Laboratory Use |
| 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 HiSeq X System is a groundbreaking sequencing platform engineered to enable population-scale whole-genome sequencing (WGS) with unmatched throughput, speed, and cost-efficiency. Designed specifically for human WGS applications, the HiSeq X system leverages patterned flow cell technology and sequencing by synthesis (SBS) chemistry to produce high-quality genomic data at an extraordinary scale. It’s the platform of choice for major genome centers and institutions engaged in large-scale genomic research.
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 98508 70860, +91 84461 74263
Optimized exclusively for human whole-genome sequencing
Up to 1.8 Tb of data in under 3 days per system
Patterned flow cell technology for ultra-high cluster density
Produces up to 600 Gb per flow cell with high coverage depth
Exceptionally low cost per genome
Fast, reliable performance with superior base calling accuracy
Seamless integration with Illumina’s BaseSpace and DRAGEN™ pipelines
UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
| Minimum Order Quantity | 5 Piece |
| Usage/Application | Laboratory Use |
| 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 |
The Illumina HiSeq 4000 System is a high-throughput sequencing platform engineered for large-scale genomic projects, delivering massive data output with speed and accuracy. Leveraging patterned flow cell technology and proven sequencing by synthesis (SBS) chemistry, it supports a broad range of applications including whole-genome sequencing (WGS), whole-exome sequencing (WES), transcriptomics, and epigenomics. The HiSeq 4000 is ideal for core facilities, population-scale studies, and high-volume research labs requiring cost-effective, ultra-high data output.
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 98508 70860, +91 84461 74263
Patterned flow cell technology for improved cluster density and throughput
Dual flow cell design enables up to 1.5 Tb of data in ~3.5 days
Flexible read length configurations (single- or paired-end)
Supports large-scale projects like WGS, RNA-seq, and ChIP-seq
Seamless integration with Illumina’s BaseSpace for cloud-based data analysis
High data accuracy and uniform coverage
Cost-effective sequencing per gigabase for population-scale studies
UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
| Usage/Application | Laboratory Use |
| Capacity | 8 Sample Plates |
| Number Of Capillaries | 96 |
| Capillary Length | 50 cm |
| Read Length | 200-400 bp |
| Sample Volume | 18537 |
| Throughput | 384 |
| Sequencing Chemistry | Pyrosequencing |
| Amplification Approach | PCR |
| Time Per Run | 20 minutes-3 hours |
| Format | 384 well |
| List No | R |
The Illumina MiSeq System is a compact benchtop next-generation sequencing (NGS) platform that integrates cluster generation, sequencing by synthesis (SBS) chemistry, and data analysis into a single instrument. It is designed for targeted and small-genome sequencing applications, offering rapid turnaround times and high-quality data.
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 98508 70860, +91 84461 74263.
Key Features:
Integrated Workflow
Rapid Turnaround Time
High Data Quality
Flexible Read Lengths
User-Friendly Interface
Compact Design
Onboard Data Analysis
Cloud Connectivity
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
| Minimum Order Quantity | 5 Piece |
| Usage/Application | Whole Exome Sequencing |
| Capacity | 16 Sample Plates |
| Brand | Nextseq |
| 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 |
| Model Name/Number | 2000 |
| List No | R |
The Illumina NextSeq 2000 is a state-of-the-art sequencing platform designed to deliver flexible, scalable, and high-throughput genomic sequencing. Utilizing the innovative NovaSeq™ Xp workflow and patterned flow cell technology, the NextSeq 2000 enables a broad range of applications including whole-genome sequencing, transcriptomics, single-cell RNA-seq, and more. With onboard secondary analysis and an intuitive interface, it simplifies complex workflows while delivering exceptional data quality and efficiency for clinical and research labs.
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 98508 70860, +91 84461 74263
Patterned flow cell technology for higher throughput and accuracy
Supports a wide variety of applications including WGS, RNA-seq, and exomes
Onboard DRAGEN™ bioinformatics for fast, integrated analysis
Flexible run configurations with P1 and P2 flow cells
Simplified user interface with touchscreen operation
Compact benchtop design with scalable output up to 330 Gb per run
Cloud-connected for streamlined data management and sharing
UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.
Product Details:
| Capacity | 8 Sample Plates |
| Number Of Capillaries | 96 Capillaries |
| Capillary Length | 50 cm |
| Read Length | 700 bp |
| Sample Volume | 43250 |
| Voltage | 220 V |
| List no. | R |
The Miniseq System is a compact, benchtop next-generation sequencing (NGS) platform designed for rapid, affordable, and accessible DNA sequencing. It is ideal for small to medium-sized labs and offers streamlined workflows for targeted sequencing, gene expression analysis, and small genome sequencing with high accuracy.
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 98508 70860, +91 84461 74263.
Key Features:
Compact benchtop design suitable for limited lab space
Fast sequencing run times (as short as 7-24 hours depending on application)
Supports targeted gene panels, amplicon sequencing, and small genome sequencing
User-friendly, streamlined workflow with integrated data analysis tools
High accuracy with Illumina’s sequencing-by-synthesis technology
Flexible throughput options tailored to smaller sample batches
Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R – Refurbished, PO – Preowned, U – Used, T – Trading, M – Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.