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Event
Revvity at ASHG Annual Meeting 2024
Exhibit Hall: November 6 – 8
Booth # 325 (next to the CoLab Theater 1)
Hours: 9:30 am – 4:30pm
Join us at the ASHG meeting 2024!
NGS workflows that work for you.
We are excited to see you again at the ASHG annual meeting 2024!
Register for the annual meeting if you haven’t already or connect with Revvity so we can personally welcome you at our booth during the conference, on your schedule!
Learn about our genomic solutions that are helping labs accelerate their discovery since last we met:
- Biobanking workflows
- NGS workflow efficiency
- Single-cell sequencing
- Reference standards
- NGS for newborn research
Showcasing technologies powered by your go-to names for instruments and reagents:
- Omni Bead Ruptor™ bead mill homogenizers
- Cellometer™ and Celleca™ image cytometers and cell counters
- chemagic™ automated DNA and RNA workflows
- LabChip™ GX Touch™ nucleic acid analyzer for quantitation and sizing
- JANUS™, Fontus ™, Zephyr™ automated liquid handlers and workstations
- NEXTFLEX™ UDI-UMIs and library prep kits, including our new line of DepleteX™ kits
- BioLegend oligo-conjugated antibodies, hashtags, and cocktails for proteogenomics
- Dharmacon™ RNAi reagents and libraries (siRNA, shRNA, miRNA, ncRNA)
- Dharmacon™ gene editing reagents and libraries (CRISPR knockout, CRISPR activation, CRISPR interference, and Pin-point™ base editing research reagents)
- Mimix™ reference standards
See you soon.
For research use only. Not for use in diagnostic procedures.
What’s New at the ASHG Annual Meeting 2024
Improved rare variant analysis
NGS sequencing provides data with inherent error rates introduced during library prep which can interfere with the identification of low-abundance variants. By incorporating the NEXTFLEX™ UDI-UMI adapters on each DNA fragment prior to amplification, variant alleles present in the original sample can be distinguished confidently from errors introduced during library preparation, target enrichment, or sequencing.
Enhanced detection of low-abundance transcripts
The highly targeted DepleteX™ CRISPR-Cas9 depletion solutions remove uninformative molecules prior to sequencing and improve your ability to detect biologically relevant transcripts in single cell sequencing, whole blood samples, and even complex communities containing host and bacteria RNA.
Low-throughput DNA extraction, library prep and sample quantitation
Designed for the automated preparation of DNA libraries directly from human whole blood, the BioQule™ Bleed to Read™ DNA Library Prep Kit offers an efficient and reliable solution for genomic research. This kit allows the creation of up to 8 uniquely dual-indexed paired-end double-stranded DNA libraries with reduced hands-on time by up to 80%.
Solutions at the booth
Come and meet our people at the ASHG meeting 2024. See a few… daily work. We don’t want to miss this opportunity at the ASHG annual meeting 2024 to meet with amazing scientists from across the globe pushing research in human genetics.
Mixer in the Mountains - networking event
Join us for this casual networking event at Flight Club on Thursday Evening to unwind from the conference. Come and meet with Revvity colleagues and product experts while enjoying some light refreshment!
Cellometer™ Ascend™ automated cell counter
A benchtop automated cell counter offering fast analysis and reliable cell counts with small sample volumes. The Cellometer™ Ascend™ is equipped with Matrix™ software, has multiple pre-defined assays, can analyze numerous cell types, and is 21 CFR Part 11 ready.
A benchtop automated cell counter offering fast analysis and reliable cell counts with small sample volumes. The Cellometer™ Ascend™ is equipped with Matrix™ software, has multiple pre-defined assays, can analyze numerous cell types, and is 21 CFR Part 11 ready.
Omni Bead Ruptor Elite™ bead mill
An advanced and easy-to-use bead mill homogenizer, the Elite is designed for grinding, lysing, and homogenizing biological samples prior to molecular extraction. Designed with a unique carriage motion, intra-tube bead movement reduce swirling and results in high-impact bead milling that helps decrease processing time and reduces risk of sample heating.
An advanced and easy-to-use bead mill homogenizer, the Elite is designed for grinding, lysing, and homogenizing biological samples prior to molecular extraction. Designed with a unique carriage motion, intra-tube bead movement reduce swirling and results in high-impact bead milling that helps decrease processing time and reduces risk of sample heating.
chemagic™ 360 automated nucleic acid extractor
A flexible, compact solution for automated nucleic extraction from diverse sample materials, the chemagic™ 360 leverages magnetic bead-based technology that offers a reliable solution to support different throughput needs and a range of downstream applications such as NGS, MPLA, genotyping, and PCR.
A flexible, compact solution for automated nucleic extraction from diverse sample materials, the chemagic™ 360 leverages magnetic bead-based technology that offers a reliable solution to support different throughput needs and a range of downstream applications such as NGS, MPLA, genotyping, and PCR.
FlexDrop™ Plus non-contact dispenser
A rapid, consistent, and flexible dispenser, the FlexDrop™ Plus permits automated low-volume liquid-handling from up to 96-source positions into 96, 384, or 1536 well plates with a dead volume of less than 1 μL. Employing a droplet verification system and positive pressure in eight independently controlled channels, each channel can dispense up to 100 droplets per second to achieve the target dispense volume.
A rapid, consistent, and flexible dispenser, the FlexDrop™ Plus permits automated low-volume liquid-handling from up to 96-source positions into 96, 384, or 1536 well plates with a dead volume of less than 1 μL. Employing a droplet verification system and positive pressure in eight independently controlled channels, each channel can dispense up to 100 droplets per second to achieve the target dispense volume.
Mimix™ reference standards
Confirm your assays are working as expected with Revvity’s Mimix™ Reference Standards. Our Mimix control materials are cell-line derived to maintain genomic complexity and mimic patient material across molecular workflows. The blended cell lines used in our Mimix reference standards contain disease-relevant variants in key cancer genes.
Confirm your assays are working as expected with Revvity’s Mimix™ Reference Standards. Our Mimix control materials are cell-line derived to maintain genomic complexity and mimic patient material across molecular workflows. The blended cell lines used in our Mimix reference standards contain disease-relevant variants in key cancer genes.
Dharmacon™ RNAi, CRISPR, and custom synthesis solutions
Revvity’s Dharmacon reagents support researchers at the DNA, RNA, and protein level with the broadest range of functional genomic tools including industry leading gene modulation and gene editing solutions to help elucidate complex biological networks for functional genomic studies from single-gene experiments to whole genome screens facilitating advancements in genetic research and therapeutic discovery. Known for almost 30 years as premier providers of synthetic oligonucleotides, our Dharmacon reagents were the first to offer algorithm designed synthetic siRNA for RNAi, and the first to offer guide RNA for CRISPR-Cas9 gene editing applications.
Revvity’s Dharmacon reagents support researchers at the DNA, RNA, and protein level with the broadest range of functional genomic tools including industry leading gene modulation and gene editing solutions to help elucidate complex biological networks for functional genomic studies from single-gene experiments to whole genome screens facilitating advancements in genetic research and therapeutic discovery. Known for almost 30 years as premier providers of synthetic oligonucleotides, our Dharmacon reagents were the first to offer algorithm designed synthetic siRNA for RNAi, and the first to offer guide RNA for CRISPR-Cas9 gene editing applications.
BioLegend TotalSeq™ antibodies
Uncover unique phenotypes and understand protein expression on a single-cell level with TotalSeq™ oligo-conjugated antibodies. Seamlessly integrate these reagents into existing single-cell sequencing protocols for simultaneous characterization of protein and RNA or protein and DNA.
Uncover unique phenotypes and understand protein expression on a single-cell level with TotalSeq™ oligo-conjugated antibodies. Seamlessly integrate these reagents into existing single-cell sequencing protocols for simultaneous characterization of protein and RNA or protein and DNA.
NEXTFLEX™ library prep reagents
The NEXTFLEX library prep reagents have optimized enzymatic and automation efficiencies to cater to our customers’ needs for cost-effective solutions to achieve robust sequencing results. They are designed to increase the flexibility and speed of library prep for customers utilizing Illumina® and Element Biosciences® sequencing platforms.
The NEXTFLEX library prep reagents have optimized enzymatic and automation efficiencies to cater to our customers’ needs for cost-effective solutions to achieve robust sequencing results. They are designed to increase the flexibility and speed of library prep for customers utilizing Illumina® and Element Biosciences® sequencing platforms.
NGS workflow for newborn research
Across the globe, there are technological gaps which can limit the scope of newborn sequencing research. With decades of laboratory expertise, Revvity’s end to end sequencing workflow – from blood spot card through final analysis – bridges these gaps, empowering newborn research beyond expectation.
Across the globe, there are technological gaps which can limit the scope of newborn sequencing research. With decades of laboratory expertise, Revvity’s end to end sequencing workflow – from blood spot card through final analysis – bridges these gaps, empowering newborn research beyond expectation.