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One of two multi-sample array formats for DNA or RNA analysis applications. With multi-sample BeadChip formats, sync wells are etched onto the surface of each substrate to a depth of approximately 3 microns prior to docking.
BeadArray Microarray technology is used in Illumina array products and scanners in a wide range of DNA and RNA analysis applications.
-Reliable data quality
-Widely applied globally, enhancing collaboration and promoting research
-Detection of chromosomal alterations and copy number variants (CNV) polymorphism
-Drive scalable workflows for large studies, including population-scale genotyping
-Integration with the Illumina sequencing system for multi-omics analysis
-Flexible content
-Source management, tracking and traceability tools are formed.
– Microarray BeadArray technology is based on 3 micron silica particles that self-assemble in microwells on one of two substrates: fiber bundles or flat silica pads. When randomly assembled on either of these substrates, the particles were evenly spaced ~5.7 microns. Each bead is covered with hundreds of thousands of copies of a specific oligonucleotide that acts as paired sequences in an Illumina experiment.
-The BeadArray Microarray technology is developed on one of two multi-sample array formats for DNA or RNA analysis applications. With multi-sample BeadChip formats, sync wells are etched onto the surface of each substrate to a depth of approximately 3 microns prior to docking. The particles are then randomly assembled and held in the microwells by Van der Waals forces and hydrostatic interactions with the walls of the well.
-Microarray is the ideal technique for examining thousands of samples to identify point mutations, structural variations or changes in gene expression and methylation. Illumina’s microarray offers many advantages such as:
Reliable data quality
Widely applied globally, enhancing collaboration and promoting research
Detection of chromosomal alterations and copy number variants (CNV) polymorphism
Drive scalable workflows for large studies, including population-scale genotyping
Integration with the Illumina sequencing system for multi-omics analysis
Flexible content
Source management, tracking and traceability tools are formed.
Technology
ILMN Microarray Technology
The 3500xL Genetic Analyzer is a 24-capillary sequencing platform that can be used for a wide variety of applications, including de novo sequencing and resequencing (mutational profiling), as well as microsatellite analysis, MLPA™, LOH, MLST, and SNP validation or screening. The majority of applications can be run on a single polymer and capillary array.
The Applied Biosystems™ 3500 Series Genetic Analyzers are specifically designed to support the demanding performance needs of validated and regulated environments while retaining the unsurpassed application versatility that life science researchers expect. The 8-capillary 3500 Genetic Analyzers continue to set the standard in capillary electrophoresis.
Disclaimer: This product is labelled for Research Use Only – Not for use in diagnostic procedures.
The QuantStudio™ 12K Flex system is a highly flexible, comprehensive real-time PCR platform that leverages the best of Applied Biosystems real-time technology in a single instrument. The QuantStudio™ 12K Flex Real-Time PCR System includes easy-to-change blocks that can accommodate OpenArray® plates, TaqMan® array cards, 384-well, 96-well, and FAST 96-well plates allowing you to select the format that is right for your project whether it’s now or in the future, for maximum flexibility and consistency in your research.
Thermo Fisher Cloud
Thermo Fisher Cloud provides scientists with a secure place to store, analyze, and share data. Applied Biosystems qPCR Analysis Modules within the Thermo Fisher Cloud are web browser-based software tools that are flexible, fast and easy to use. These software tools are compatible with Mac or PC as well as most Applied Biosystems instrument file types.
The QuantStudio™ 12K Flex System’s intuitive software, easy touch screen setup, automation integration, effortless block exchange, and easy-to- use OpenArray® components are designed to let you get started right away and reduce hands on time. Plan for the future and save time, money, and space in your lab with the only all-in-one qPCR instrument enabling a broad range of applications with maximum throughput.
Label or Dye 6-FAM, LIZ, NED, SID, TAZ, VIC Product Line GlobalFiler™ Product Type PCR Amplification Kit Shipping Condition Dry Ice Target Loci Amelogenin, CSF1PO, D10S1248, D12S391, D13S317, D16S539, D18S51, D19S433, D1S1656, D21S11, D22S1045, D2S1338, D2S441, D3S1358, D5S818, D7S820, D8S1179, DYS391, FGA, IQC-Large, IQC-Small, SE33, TH01, TPOX, Y indel, vWA
• Consolidated Workflow: DNA denaturation and bisulfite conversion process in one step.
• High Yield: Desulfonation and purification on a spin-column allows elution of bisulfite-converted DNA in as little as 10 µl.
• Suitable for Various Downstream Applications: Bisulfite-converted DNA can be robustly PCR amplified for downstream analyses including endonuclease digestion, sequencing, microarrays, etc.
NovaSeq X also significantly reduces waste and environmental impact, reflecting Illumina’s commitment to using its technology to support the health of people and the planet. NovaSeq X features a 90% reduction in packaging waste and weight and 50% reduction in plastic usage compared to NovaSeq 6000.
Zymot with simple operation process, helps to collect high-quality sperm, improve the efficiency of Assisted Reproduction (IVF, IUI, ICSI).
Zymot with simple operation process, helps to collect high-quality sperm, improve the efficiency of Assisted Reproduction (IVF, IUI, ICSI).
Assisted Reproductive 
Prenatal screening 
New-born screening 
Screening 
Diagnosis 
Early detection 
Monitoring 
Illumina infectious diseases testing group 
GeneProof infectious diseases testing group 
Panagene infectious diseases testing group 
Digital forensics 
Inspection of Ballistics and Mechanical Traces 
Document examination 
Crime scene examination 
