Latest: Achieve accuracy and reliability in cell counting
Latest: Beckman Coulter expands DxI 9000 Immunoassay Analyzer menu
Latest: Bioanalytic breakthroughs redefine drug development
Latest: How to navigate the lab digitalization journey
Latest: SelectScience Analytical Science Summit 2024 – Taking place today!
Latest: Streamline food safety analysis through automation
Latest: Malvern Panalytical launches Revontium at Analytica 2024
Overcome anti-doping analysis obstacles
Achieve accuracy and reliability in cell counting
Next-generation instrument screens for hemoglobin disorders in newborns
ESCMID modernizes its branding and communications
Analytical measurements supporting cellular therapies
Evolution in gene therapy vector analysis
Managing the risk of nitrosamines in medicinal drugs
Your essential guide to preparative LC
Efficacy of cell reprogramming using 3D spheroid model
New microplate platform with cryopreserved 3D tumor spheroids
Mitigation of liver toxicity with the Akura Twin Microplate
Akura Immune Flow Chip microfluidic 3D spheroid system
How to Buy Cell Counting Equipment
Microplate Readers
How to Buy Microscopy Equipment
How to Buy Water Purification Technology
How to Buy Clinical Laboratory Automation Technology
Biophysical Characterization Technology
ABRF 2024 Annual meeting
21 Apr 24 - 24 Apr 24
Immuno-Oncology Summit...
23 Apr 24 - 25 Apr 24
ESCMID Global 2024
27 Apr 24 - 30 Apr 24
Immunology2024
03 May 24 - 07 May 24
CYTO 2024
04 May 24 - 08 May 24
Advertisement
Reliable detection of copy number changes and loss of heterozygosity on a single array for haematological malignancies and solid cancers. The CytoSure Cancer +SNP array delivers: ■ Flexible choice of reference sample ■ Confident de... Read more...
OGT can help you get straight to the variant of interest with whole exome or custom targeted sequencing services. Genefficiency™ targeted sequencing services are designed to be different, leading you all the way from project conceptio... Read more...
A high-quality RNA sequencing service designed to deliver cost-effective and rapid access to meaningful transcriptomics results. The Genefficiency™ RNA-Seq Service from OGT provides a new level of assay customisation to ensure each ex... Read more...
Reliable detection of copy number changes for research into a range of genetic disorders. CytoSure Molecular Arrays are designed to accurately identify small intragenic copy number variations (CNVs) in genes associated with a variety ... Read more...
An expanding portfolio of NGS panels for research into haematological and solid tumour cancers, as well as library preparation kits for the accurate detection of a wide range of genetic aberrations Read more...
The SureSeq™ Myeloid Plus NGS Complete Workflow combines the rapid Universal NGS Workflow hybridisation-based target enrichment method together with OGT’s expert bait design to detect 49 key genes implicated in myeloid disorde... Read more...
The SureSeq™ CLL + CNV Panel has been designed in collaboration with recognised cancer experts to detect 13 key genes and 5 chromosomal regions implicated in CLL progression (Table 1). The SureSeq CLL + CNV Panel alleviates the burd... Read more...
Myeloproliferative neoplasms (MPNs) are a heterogeneous group of diseases characterised by the overproduction of one or more types of blood cells. The SureSeq™ Core MPN Panel has been designed in collaboration with recognised cancer... Read more...
The complete library preparation solution for unparalleled next generation sequencing (NGS) results. Based on scientists’ feedback, we have redesigned our workflow to ensure scientists achieve the most optimal NGS libraries, with on... Read more...
High quality, reliable and easy-to-use DNA probes for fluorescence in situ hybridisation (FISH) Read more...
CytoCell myProbes® is a custom design and manufacture service that provides unique fluorescence in situ hybridisation (FISH) probes using the BAC-2-FISH™ process. Read more...
IVDR certified probes now available! Read more...
Interpret is OGT’s powerful and easy-to-use next-generation sequencing analysis solution. Read more...