This microarray offers comprehensive, genome-wide coverage of pharmacogenomic (PGx) markers and features a fast, highly scalable automated workflow.
Automation capability | Liquid Handling Robots, Automated Array Loader |
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Method | Genome-Wide Genotyping Array, High-Throughput Genotyping Array |
Nucleic acid type | DNA |
Specialized sample types | Blood |
Species category | Human |
Systems | iScan System |
Technology | Microarray |
Variant class | Single Nucleotide Polymorphisms (SNPs), Chromosomal Abnormalities, Insertions-Deletions (indels), Copy Number Variants (CNVs) |
Instrument | Recommended number of samples | Read length |
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Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit | Infinium Global Diversity Array with Enhanced PGx | Infinium Global Clinical Research Array-24 v1.0 Kit | Infinium Global Screening Array-24 Kit | |
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Automation capability | Liquid Handling Robots, Automated Array Loader | Liquid Handling Robots, Automated Array Loader | Liquid Handling Robots | Liquid Handling Robots, Automated Array Loader |
Method | Genome-Wide Genotyping Array, High-Throughput Genotyping Array | Genome-Wide Genotyping Array | Genome-Wide Genotyping Array, High-Throughput Genotyping Array | |
Nucleic acid type | DNA | DNA | DNA | DNA |
Specialized sample types | Blood | Blood | Blood | Blood, FFPE Tissue, Buccal Swabs, Saliva |
Species category | Human | Human | Human | Human |
Systems | iScan System | iScan System | iScan System | iScan System |
Technology | Microarray | Microarray | Microarray | Microarray |
Variant class | Single Nucleotide Polymorphisms (SNPs), Chromosomal Abnormalities, Insertions-Deletions (indels), Copy Number Variants (CNVs) | Single Nucleotide Polymorphisms (SNPs), Chromosomal Abnormalities, Insertions-Deletions (indels), Copy Number Variants (CNVs) | Single Nucleotide Polymorphisms (SNPs), Structural Variants, Copy Number Variants (CNVs) |
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx-24 v1.0 Kit
Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24 v1.0 Kit (24 Samples)
20068341
Includes one, 24-sample BeadChip and reagents for amplifying, fragmenting, hybridizing, labeling, and detecting 24 DNA samples and software for generating metabolizer status and star allele reports. Requires 200 ng DNA for input. Each kit is processed as a single batch.
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Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24 v1.0 Kit (96 Samples)
20068342
Includes four, 24-sample BeadChips and reagents for amplifying, fragmenting, hybridizing, labeling, and detecting 96 DNA samples and software for generating metabolizer status and star allele reports. Requires 200 ng DNA for input. Each kit is processed as a single batch.
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Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24 v1.0 Kit (1152 Samples)
20068343
Includes 48, 24-sample BeadChips and reagents for amplifying, fragmenting, hybridizing, labeling, and detecting 1152 DNA samples and software for generating metabolizer status and star allele reports. Requires 200 ng DNA for input. Each kit is processed as a single batch.
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Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24+ v1.0 Kit (24 samples)
20068357
This kit offers 1 BeadChip along with reagents for processing 24 DNA samples and includes star allele and metabolizer status results. It offers exceptional coverage of key pharmacogenomic markers and provides a cost-effective and highly scalable workflow to support population-scale clinical research studies. IMPORTANT: This EX BeadChip is compatible with the Infinium Amplification System and the Infinium Automated Pipetting System with ILASS.
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Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24+ v1.0 Kit (96 samples)
20068358
This kit offers 4 BeadChips along with reagents for processing 96 DNA samples and includes star allele and metabolizer status results. It offers exceptional coverage of key pharmacogenomic markers and provides a cost-effective and highly scalable workflow to support population-scale clinical research studies. IMPORTANT: This EX BeadChip is compatible with the Infinium Amplification System and the Infinium Automated Pipetting System with ILASS.
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Infinium Global Clinical Research Array with Enhanced PGx + interpretation-24+ v1.0 Kit (1152 samples)
20068359
This kit offers 48 BeadChips along with reagents for processing 1152 DNA samples and includes star allele and metabolizer status results. It offers exceptional coverage of key pharmacogenomic markers and provides a cost-effective and highly scalable workflow to support population-scale clinical research studies. IMPORTANT: This EX BeadChip is compatible with the Infinium Amplification System and the Infinium Automated Pipetting System with ILASS.
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Illumina Hybridization Oven (110V)
SE-901-1001
Includes a rotating hybridization wheel with variable rotation speed of 5–60 rpm and a temperature range from 0°C to 100°C. Holds up to 24 BeadChips at one time. (110 V)
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Illumina Hybridization Oven (220V)
SE-901-1002
Includes a rotating hybridization wheel with variable rotation speed of 5–60 rpm and a temperature range from 0°C to 100°C. Holds up to 24 BeadChips at one time. (220 V)
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Infinium XT Hybridization Chamber (1)
20011755
Infinium XT Hybridization Chamber supporting the hybridization of DNA samples to BeadChips.
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This BeadChip is an excellent solution for pharmacogenomic studies, and precision medicine research, including studies in diverse populations and underrepresented ethnic groups.:
Infinium EX format compatible with powerful Infinium liquid handling instruments with advanced software.
Dr. Julio Monterrey is a Stanford-trained, board-certified psychiatrist and neuroscientist who specializes in diagnosing and treating complex cases.
Read MoreDevin Absher, PhD has studied the genetics of complex human traits and diseases for over 20 years and was a pioneer in genome-wide and epigenome-wide association studies.
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