DNA and RNA quantitation and sizing can be done in seconds using automated capillary electrophoresis separation. The LabChip® GX Touch™ nucleic acid analyzer’s microfluidic technology generates reproducible, high-resolution data and is optimal for
For research use only. Not for diagnostic procedures.
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The comprehensive solution for genomic sizing and quantitation
With complete analysis of genomic material in about 30 seconds, the LabChip® GX Touch™ nucleic acid analyzer eliminates the nucleic acid quantitation workflow bottleneck. High-resolution analysis provides exact sizing and quantitation of DNA fragments and smears down to 5 bp from samples as small as 2 pg/μL.
The system offers a broad variety of DNA analysis options, including the NGS 3K assay, which provides unparalleled genomic data quality with minimal input requirements. This high degree of sensitivity also makes it the ideal instrument for gDNA, cfDNA, and PCR-free DNA quantitation, where concentrations are low, samples are precious and their preservation is essential.
When used for RNA analysis, it provides critical RNA metrics such as peak heights, peak areas, and concentration, which are used to determine an RQS (RNA Quality Score) for each sample. The RQS calculation has been validated to correlate with Agilent’s RIN (RNA Integrity Number) and follows the same 0-10 scale rating.
|21 CFR Part 11 Compatible||Yes|
|Model Name||LabChip GX Touch HT Nucleic Acid Analyzer|
|Product Brand Name||LabChip®|
PerkinElmer and 10x Genomics have created a complete automated workflow for long-read sequencing which maximizes high molecular weight gDNA extraction for a variety of sample types including saliva, DBS, blood, and plasma.
Enhance scalability of mutation detection with on-target gene editing PCR and the LabChip GX® Touch™ Nucleic Acid Analyzer.
Increase efficiency without sacrificing quality of genomics analysis with the LabChip® GX Touch™ nucleic acid analyzer
This flyer gives the overview of PerkinElmer NGS workflow solutions from extraction to analysis.
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