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Poster Icon   Scientific Poster
Whole Genome Sequencing Improves Clinical Diagnosis in Patients with a Suspected Genetic Disorder(s): Diagnostic yield from 386 cases
The benefits of WGS promotes it a promising alternate as a first-tier diagnostic test for patients at early stage is highlighted in this poster
Brochure Icon   Brochure
Solutions for liquid scintillation counting
Guide to modern high-throughput immuno-oncology assays using the Celigo image cytometer.
Publication Icon   Literature - Publication Review
A lung tropic AAV vector improves survival in a mouse model of surfactant B deficiency
Researchers design an adeno-associated virus (AAV) 6 capsid that demonstrates efficiency in lung epithelial cell transduction in a mouse model validated using optical imaging.
Brochure Icon   Brochure
Automation pipette tips and consumables catalogue for Revvity Liquid Handlers
Automation pipette tips and consumables designed, validated, and approved for compatibility with Revvity liquid handlers.
Application Note Icon   Application Note
Excellent sensitivity from the EnVision Nexus multimode plate reader for AlphaLISA detection
This application note demonstrates the AlphaLISA detection capabilities of the EnVision Nexus and compares it to the EnVision 2105.
Poster Icon   Scientific Poster
Utilizing Advanced Genomic Technologies to Identify Dual Diagnoses
The ability of whole genome sequencing and the whole exome sequencing helps in Nuclear and mito genome detection, SNV and CNV detection and multiple diagnoses
Poster Icon   Scientific Poster
Extending and Adapting the Functions of Genetic Laboratories During the COVID-19 Pandemic- Challenges and Successes
Given the current global awareness of respiratory virus activity and spread, there is a growing demand for new and expanded testing. This poster explains the need to explore the new tests to pivot between COVID test and Rare disorders with innvoation
Other Icon   Other
Whole genome sequencing is a powerful “one-stop shop” screening assay for uncovering undiagnosed conditions in apparently healthy pediatric cohort
This abstract indicates that WGS screening can serve as a “one-stop shop” for uncovering a wide range of looming genetic conditions in apparently healthy children, this way enabling the family and treating clinicians to take timely appropriate actions to maximize their healthcare outcomes and inform future reproductive decisions.
Brochure Icon   Brochure
Cellometer Ascend automated cell counter brochure
Brochure describing the Cellometer Ascend automated cell counter.
Application Note Icon   Application Note
Optimizing 384-well qPCR plate preparation while decreasing costs
How to decrease 384-well qPCR plate preparation time and costs using FlexDrop iQ Non-Contact Dispenser. qPCR solutions compared by the Centre for Cancer Biology.
Application Note Icon   Application Note
Phenotypic profiling of autophagy using high content profiler
Using an autophagy assay as an example, this study describes the validation of a phenotypic image and data analysis workflow.
Case Study Icon   Case Study
Improving the throughput of a neuroprotection assay using the opera phenix high content screening system
Download the case study to learn how primary neuron morphology is analyzed in a straightforward approach using Harmony® software and careful assay optimization can increase throughput, and minimize the data burden, without compromising assay performance.
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