Department of Molecular Biology
The Department of Molecular Biology at AEGEAN Medical. In recent years, molecular biology has been used increasingly frequently for the screening and diagnosis of diseases that are either difficult to diagnose using other methods or are caused by defects in an individual’s genetic material. Special mention should be made of Molecular Microbiology, a field that has gained particular diagnostic value due to the SARS-CoV-2 pandemic. Cytogenetic testing (karyotyping) of peripheral blood and other biological materials is performed. Viruses and microbes are detected and identified in various biological materials. Finally, various mutations and polymorphisms that cause diseases are tested. In this department, tests such as the following are performed:
Cytogenetics
In the Department of Molecular Biology at AEGEAN Medical.
FISH (Fluorescence In Situ Hybridisation)
Peripheral Blood Karyotype
Chorionic Villus Karyotype
Amniotic Fluid Karyotype
Miscarriage Tissue Karyotype
Tissue Karyotyping
Bone Marrow Karyotyping
Subtelomeric Chromosome Analysis
Molecular Microbiology
Molecular Detection of SARS-CoV-2 (COVID-19) via RT-PCR
Epstein-Barr Virus (EBV)
QF-PCR (Amniotic Fluid-Chorionic Villi)
Cytomegalovirus (CMV)
Adenovirus Detection
Enterovirus (EV) Detection/Typing
Rubella Virus Detection
Detection and Typing of Human Papillomavirus (HPV)
Parvovirus B19 Detection
Toxoplasma gondii Detection
Herpes Simplex Virus 1-2 (HSV 1-2)
Hepatitis B Virus (HBV) Detection/Quantification
Hepatitis C (HCV) Detection/Quantification/Genotyping
Influenza Virus Detection (Influenza A, B, H1N1)
Mycobacterium tuberculosis
Mycoplasma pneumoniae (Mycoplasma pneumoniae)
Mycoplasmas (Mycoplasma hominis, Ureaplasma urealyticum)
Chlamydia trachomatis
Chlamydia pneumoniae
Molecular Genetics
HLA-B27 (PCR)
Cystic Fibrosis (CF) 4 Mutations (ME ΔF508)
Cystic Fibrosis (CF) 50 Mutations (ME ΔF508)
NON-SYNDROMIC HEARING LOSS (35delG)
BETA-THALASSEMIA (PCR)
GENETIC THROMBOPHILIA 3 MUTATIONS (ME MTHFR-577)
GENETIC THROMBOPHILIA 13 MUTATIONS (ME MTHFR-577 & 1298)
FACTOR V-LEIDEN (G1691A)
FACTOR V-R2 (H1299R)
FACTOR II-PROTHROMBIN (G20210A)
FACTOR XIII (V34L)
APO B (R3500Q)
APO E GENOTYPE (E2/E3/E4)
MTHFR (C677T)
MTHFR (A1298C)
PAI-1 (4G/5G)
B-FIBRINOGEN (G455A)
ACE MUTATION (I/D)
GPIIIa – FIBRINOGEN RECEPTOR (HPA-1)
GPIba – F-vW RECEPTOR (HPA-2)
GPIa – COLLAGEN RECEPTOR (HPA-5)
