3499 results found for "Advanta RNA-Seq NGS Library Prep Kit"
Advanta™ Immuno-Oncology Gene Expression Assay
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Advanta RNA-Seq XT NGS Library Prep Kits
Transform your RNA sequencing productivity with nanoscale automation …
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consumable
Advanta™ RNA-Seq NGS Library Prep Kit
This kit enables the preparation of NGS-ready, dual-indexed, full-length cDNA libraries of poly(A) RNA utilizing total RNA isolated from human, mouse, or rat for subsequent sequencing analysis. The kit contains four 48.Atlas™ IFCs and includes sufficient 3′ and 5′ primer indexes, reagents for generating strand-specific cDNA libraries, and Control Line Fluid for up to 48 samples (up to 6 libraries) per IFC. The 4 IFCs can accommodate a total of 192 samples (up to 24 libraries). …
Product #: 101-9187
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Advanta™ RNA-Seq XT NGS Library Prep Kit II (101-9959)
This kit uses a polyadenylated [poly(A)] enrichment approach to prepare NGS-ready, full-length cDNA libraries from total RNA. The kit contains sufficient 48.Atlas™ IFCs (4 per kit), reagents, Control Line Fluid, and unique dual indexes (UDIs) to generate libraries for 192 samples, and it includes 4 sets of 1–48 UDI barcodes. …
Product #: 101-9959
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consumable
Advanta™ RNA-Seq XT NGS Library Prep Kit (101-9950)
This kit uses a polyadenylated [poly(A)] enrichment approach to prepare NGS-ready, full-length cDNA libraries from total RNA. The kit contains sufficient 48.Atlas™ IFCs (4 per kit), reagents, Control Line Fluid, and unique dual indexes (UDIs) to generate libraries for 192 samples, and it includes 4 sets of 1–48 UDI barcodes. …
Product #: 101-9950
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Software
Advanta RNA-Seq Library Normalization Workbook V C3
This custom Microsoft® Excel® workbook is designed for use with the Advanta™ RNA-Seq NGS Library Prep Kit and Advanta RNA-Seq XT NGS Library Prep Kits with the Juno™ system to automate calculations and tracking of volume adjustment requirements of sample libraries prior to pooling.
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Genomics and Gene Expression
Enhance your productivity with high-performance solutions …
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brochure
Advanta Solid Tumor NGS Library Prep Assay
To advance our understanding of cancer and make strides toward improved patient care, researchers have a growing need to interrogate somatic mutations, often from limited quantities of available samples.