Genomics
There’s no question that genomics is one of the most exciting fields in life science.
Whether you are working on the advancement of gene therapies or personalized medicine, or using with technologies such as qPCR, next generation sequencing (NGS), and CRISPR/Cas9 genome editing chances are you and your colleagues are busy. Avantor offers a wide range of efficient solutions so you can concentrate on your important work.
Genomics Workflows
Avantor has a comprehensive list of equipment, products, and supplies to meet your needs.
Nucleic Acid Purification & Measurement
DNA samples are purified by lysating (bursting or cutting) a cell or cell structure from desired samples using lab procedures to isolate the nucleic acids from its contaminants. Purifying DNA samples from contaminants also extends their shelf-life and reduces the probability of error when it comes to research results.
Avantor can help you source high-quality nucleic acid purification systems that are simple to operate and generate rapid results. Here are some choices below.
Amplification
To study or detect individual genes or specific DNA of interest, obtaining a large quantity of nucleic acid for study is often necessary. Rather than isolate a single copy of the target DNA from a large number of cells, it is often more useful to generate multiple copies of a target from a single molecule of DNA or mRNA, via an in vitro amplification method.
Polymerase Chain Reaction (PCR) is the most common DNA amplification method in molecular biology, Avantor’s product portfolio features a large selection of Genomic tools, solutions and resources geared towards this powerful method. Review a variety of genomics resources below that can deliver successful amplification for your lab’s research.
Sequencing in genomic life sciences
Sequencing is considered to be the “gold standard” method for the identification of known (as well as unspecified) variants in genomic DNA.
Broadly speaking, there are two types of DNA sequencing: shotgun and high-throughput.
Shotgun (Sanger) sequencing is the more traditional approach, which is designed for the entire sequencing of chromosomes or long DNA strands with more than 1000 base pairs. It involves a rapidly expanding firing pattern to read the DNA in short fragments of 100 to 1000 base pairs, which are then overlapped with a computer analysis system.
High-throughput is the next-generation method of DNA sequencing (NGS), which has led to the rapid acceleration of DNA sequencing and broadened knowledge in the field. It can produce thousands of sequences simultaneously, which significantly lowers the cost of the technique.
Sequencing supplies from industry leaders are available, affordable, and easy to use whether your lab utilizes Sanger Sequencing or Next-Generation Sequencing. Avantor’s tools and resources can help.
Electrophoresis & Detection
Analysis of a DNA sequence can be accomplished via a method called electrophoresis.
Electrophoresis is a term that basically describes the movement of molecules via an electric current and separation of those molecules based on size. You can skillfully perform electrophoresis and detect reliable data with Avantor’s wide array of Genomic life sciences tools and solutions from trusted brands.
DNA/RNA Modification, Cloning & Delivery
Genetic modification differs from cloning. Cloning creates an exact copy of all or part of an organism's DNA, while genetic modification makes changes to existing DNA to create a new, modified version of the genome.
Find everything your lab needs for DNA/RNA modification, cloning, and delivery. From DNases to transfection reagents, Avantor offers all the essential tools.