​Molecular Genetics Research Laboratory:​


The Molecular Genetics Research Laboratory is dedicated to studying and analyzing nucleic acids at the molecular level with the aim of understanding gene structures and genetic changes in living organisms. This laboratory enables the exploration of genes and genomes, analyzing gene sequencing and determining the effects of genetic variations on physiology and diseases.

The laboratory facilities are equipped with advanced equipment and sophisticated techniques, such as gene sequencing analyzers and DNA cloning devices, allowing for the precise extraction, replication, and analysis of genes.

The research team in this laboratory includes molecular geneticists, researchers, and specialists who work closely to analyze data and draw conclusions. This laboratory is considered a vital center for innovation and development in the field of molecular genetics, contributing to providing new insights into the relationship between genes and biological phenomena. It plays a role in advancing our understanding of genetic diseases and opportunities for developing targeted treatments.

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 Services Provided:

 

  1. Gene Sequencing Analysis:

Providing gene sequencing analysis services to determine the structure and sequence of nucleic acids for important genes.

 

  1. DNA Cloning (PCR):

Conducting PCR tests to replicate and amplify specific genes for diagnostic or research purposes.

  1. Genetic Testing Analysis:

Offering genetic testing services to assess gene-related risks and verify the presence of specific genetic changes.

  1. Gene Expression Analysis:

Studying gene expression levels and methods to understand their impact on cellular functions and metabolism.

  1. Evaluation of Genetic Mutations:

Discovering and analyzing genetic mutations to understand their functional and health implications.

  1. Whole Genome Analysis:

Performing comprehensive genome analysis to examine the entire gene sequence and identify genetic variations.

 

  1. Early Diagnosis Tests:

Providing diagnostic tests to determine the risks of inheriting genetic diseases at an early stage.

 

Available Devices:

  • Next Generation sequencer
  • RT-PCR
  • PCR
  • Gel Electrophoresis
  • Genetic Analyzer (Sanger Sequencer)
  • Qiacube Automated Nucleic Acid Extraction
  • Cytoscan Microarray