HUMAN GENETICS
40 eur | |
RNA extraction with verification | 40 eur |
CHROMOSOMAL ABERRATIONS
INHERITED RARE DISEASES
1 200 eur | |
Custom analysis of a human gene One exon |
100 eur 294 eur 588 eur |
Alpha-1 Antitrypsin Deficiency
Detection of S and Z mutations in А1АТ* |
186 eur |
Detection of F508del CFTR mutation* | 127 eur |
Detection of the 7 most common CFTR mutations* | 294 eur |
Prenatal detection of cystic fibrosis* | 186 eur |
Screening of the CFTR gene 2* (exons: 2,6b,8,14b,16,17a,18, 22,23,24) | 931 eur |
Screening of the CFTR gene 1* (exons: 1,3,4,5,6a,7,9,10, 11,12,13,14a,15,17b,19,20,21) | 1323 eur |
Cytochrome c oxidase deficiency
Molecular diagnosis of cytochrome c oxidase deficiency (p.Glu140Lys in SCO2 gene) | 74 eur |
Molecular diagnosis of dystrophic epidermolysis bullosa (c.425A>G in COL7A1) | 74 eur |
Molecular diagnosis of familial Mediterranean fever | 74 eur |
Fumarase deficiency / Reed’s syndrome
Molecular diagnosis of fumarase deficiency / Reed’s syndrome | 391 eur |
Molecular diagnosis of fumarase deficiency / Reed’s syndrome in a blood relative | 74 eur |
Molecular diagnosis of Gaucher disease | 391 eur |
Molecular diagnosis of Gaucher disease in a blood relative | 74 eur |
Molecular diagnosis of glycogen storage disease type I | 500 eur |
Molecular diagnosis of glycogen storage disease type Ia | 244 eur |
Molecular diagnosis of glycogen storage disease type Ib | 294 eur |
Molecular diagnosis of glycogen storage disease type I in a blood relative | 74 eur |
MSUD (Maple syrup urine disease)
Molecular diagnosis of MSUD (Maple syrup urine disease) | 588 eur |
Molecular diagnosis of MSUD (Maple syrup urine disease) - BCKDHA gene | 294 eur |
Molecular diagnosis of MSUD (Maple syrup urine disease) - BCKDHB gene | 382 eur |
Molecular diagnosis of MSUD (Maple syrup urine disease) in a blood relative | 74 eur |
Detection of mutations in the PAH gene | 380 eur |
Congenital adrenal hyperplasia
Detection of mutations, conversions and large deletions of the CYP21A2 gene | 224 eur |
Detection of mutations in the CYP21A2 gene - in the family member | 74 eur |
Molecular diagnosis of Shwachman-Diamond syndrome | 118 eur |
Tyrosine hydroxylase deficiency
Molecular diagnosis of tyrosine hydroxylase deficiency | 500 eur |
Molecular diagnosis of tyrosine hydroxylase deficiency in a blood relative | 74 eur |
Detection of mutations in β- globin genes* | 180 eur |
Detection of mutations in α- globin genes* | 140 eur |
Detection of mutations in α- and β- globin genes in the family member* | 75 eur |
Prenatal detection of thalassemia syndromes* | 75 eur |
Analysis of variants of UGT1A1*28significant as a diagnostic marker in Gilbert 's syndrome and pharmacogenetic marker during irinotecan therapy |
82 eur |
HEMATOLOGICAL MALIGNANCES
MALE INFERTILITY
Detection of the presence of structural and numerical aberrations of sex chromosomes |
455 eur |
The detection of the presence of structural and numerical aberrations of sex chromosomes |
182 eur |
Detection of numerical aberrations of chromosomes X, Y, 13, 18 and 21 by FISH |
|
46 eur | |
70 eur | |
70 eur | |
WOMEN'S REPRODUCTIVE HEALTH
THROMBOPHILIA
Thrombofilic set |
|
Thrombofilic set – 1 mutation* | 65 eur |
Thrombofilic set – 2 mutations* | 90 eur |
Thrombofilic set – 3 mutations* | 160 eur |
Thrombofilic set – 4 mutations* | 175 eur |
PHARMACOGENETICS
NUTRIGENETICS
VETERINARY
Analysis of bovine k – CASEIN gene variants |
38 eur |
Analysis of bovine ß – LACTOGLOBULIN gene variants |
38 eur |
Molecular diagnostics of BLAD (Bovine Leukocyte Adhesion Deficiency) |
46 eur |
Molecular diagnostics of Porcine Stress Syndrome (PSS) |
46 eur |
GMO TESTING
MICROBIOLOGY
Purchase of the reference strain |
98 eur |
"DNK fingerprinting" analysis microorganisms |
154 eur |
Identification of bacterial species by 16s rDNA sequencing a) DNA isolation |
124 eur 25 eur |
on request | |
PFGE genotyping |
588 eur |
Determining the total number of viable bacteria / yeast sample |
39 eur |
Molecular identification of cyanobacteria and fungi a) PCR analysis |
100 eur 25 eur |
Phylogenetic analysis (up to 3 sequences) |
49 eur 10 eur |
TOXICOLOGY
COURSES
Remark:
*Services accredited at the Accreditation Body of Serbia in accordance with the requirements SRPS ISO/IEC 17025:2017 (accreditation number 01-363).
CONTACT:
Phone: + 381 64 80 44 095
E-mail: usluge@imgge.bg.ac.rs
All payments are made at the account: 160-350089-28
Services are performed by the Sector for Laboratory Investigations, which was formed on 24th January 2011 by the Institute’s Governing Board.
Sector for Laboratory Investigations performs genetic testing on the following samples:
- plant material (seed, food and feed)
- human biological samples (blood, bone marrow, buccal swab, amniotic fluid, chorionic villi, DNA samples, cytogenetic slides, semen)
- microorganism samples
- extracts and pure compounds
- animal samples (blood, DNA)
Management
- dr Branko Tomić, Head
- dr Jelena Samardžić, Vice Head
- dr Maja Stojiljkovic, Development Management