Genomic Research

Exploring the Foundations of Life

Genomic research investigates the molecular instructions encoded within DNA and RNA to understand biological functions and develop groundbreaking scientific and medical solutions. This field relies on advanced techniques and tools across several key domains: DNA/RNA Isolation & Purification, PCR and Amplification, Sequencing and Library Preparation, Gene Editing and Mutagenesis, and Epigenetic Analysis.
What is DNA?
Deoxyribonucleic acid (DNA) is the molecular blueprint for life, encoding instructions that guide the development and function of almost all living organisms. Structurally, DNA is a double-stranded helix formed by four nucleotide bases: adenine (A), thymine (T), cytosine (C), and guanine (G). These bases pair specifically (A with T, C with G) to create a complementary sequence. The order of these bases determines the genetic instructions within an organism.
What is a Genome?
A genome refers to the entire set of an organism's DNA, comprising billions of base pairs in humans. Encoded within the genome are genes, which provide the instructions for synthesizing proteins. These proteins form the building blocks of cellular structures and regulate vital biochemical processes. Mutations or changes in DNA can disrupt normal protein function, leading to conditions such as cancer and genetic disorders.
How does CRISPR-Cas9 contribute to genomic research?
CRISPR-Cas9 is a precise gene-editing tool that allows scientists to modify DNA sequences. It is widely used to study gene functions, create disease models, and develop potential therapies for genetic disorders.