DNA Tests

Showing 41 – 60 out of 173

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Tick Thumbnails Products Price Quantity Action
Cystic Fibrosis Middle East Panel (10 exons)
Cystic Fibrosis Middle East Panel (10 exons)
Sample Type : Whole Blood Methodology : Gene amplification – inverse hybridisation (Innolipa) TAT : 15 Days
3.750,00 د.إ
Cystic Fibrosis Mutation Screening (delF508)
2.400,00 د.إ
Cystic Fibrosis Single Mutation
Cystic Fibrosis Single Mutation
Sample Type : Whole Blood Methodology : Gene amplification – inverse hybridisation (Innolipa) TAT : 10 Days
2.150,00 د.إ
Cytomegalovirus (CMV) (PCR) (CSF)
Cytomegalovirus (CMV) (PCR) (CSF)
Sample Type : C.S.F Methodology : Real-time PCR TAT : 15 Days
1.050,00 د.إ
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Cytomegalovirus (CMV) PCR Test – Fast & Accurate CMV Detection
Cytomegalovirus (CMV) PCR Test is a highly sensitive and specific test designed to detect the presence of CMV DNA in blood, urine, or other bodily fluids using advanced polymerase chain reaction (PCR) technology.Sample Type : Whole BloodMethodology : Real-time PCRTAT : 15 Days
1.050,00 د.إ
Determination of Biological age using telomeric length studies
2.200,00 د.إ
DNA methylation pathway extended profile
5.900,00 د.إ
DUCHENNE/BECKER MUSCULAR DYSTROPHY (DMD/BMD) GENE MUTATION
2.800,00 د.إ
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Epstein-Barr Virus (EBV) PCR Test – Accurate & Fast Viral Detection
Epstein-Barr Virus (EBV) PCR test is a highly sensitive and specific molecular diagnostic tool designed to detect EBV DNA in blood or tissue samples. Sample Type : Whole BloodMethodology : Real-time polymerase chain reaction (PCR)TAT : 15 Days
1.450,00 د.إ
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Epstein-Barr Virus (EBV), Quantitative, PCR
 Sample Type : Whole BloodMethodology : Real-time polymerase chain reaction (PCR)TAT : 3 Days
5.500,00 د.إ
F13A1 V34L
1.520,00 د.إ
Factor V Leiden Mutation Analysis
1.600,00 د.إ
FGB G455A
1.520,00 د.إ
Focus Fusion Panel 52 Genes
5.500,00 د.إ
Fragile X (FMR1) Mutation Screen (L)
Fragile X (FMR1) Mutation Screen (L)
The Fragile X (FMR1) Mutation Screen (L) is a genetic test designed to detect mutations in the FMR1 gene, which are associated with Fragile X syndrome, a leading cause of inherited intellectual disability and autism. This screening identifies CGG repeat expansions, distinguishing between normal, premutation, and full mutation alleles. Key benefits include early detection for informed reproductive decisions, risk assessment for carriers, and guidance for personalized medical management. Utilizing advanced molecular techniques, the test ensures high accuracy and reliability. Ideal for individuals with a family history of Fragile X or unexplained developmental delays, this screening provides critical genetic insights for proactive healthcare planning.
3.400,00 د.إ
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Fragile-X Syndrome Genetic Test – Accurate Lab Screening for Inherited Conditions
Detect Fragile-X Syndrome with a lab test that identifies FMR1 gene mutations linked to intellectual disability and developmental delays.Sample Type : Whole BloodMethodology : Direct Mutation Analysis by PCR and Southern Blot AnalysisTAT : 30 Days
6.250,00 د.إ
Friedreichs Ataxia
2.800,00 د.إ
Gastro Intestinal(G.I) -Clostridium difficile + ToxA + ToxB Panel- 3 Parameters (Real Time PCR)- Clostridium difficile, Toxin A genes, Toxin B genes
750,00 د.إ
Gastro Intestinal(G.I) -Comprehensive Panel -21 Parameters (Real Time PCR)-Shigella spp, Salmonella spp, Campylobacter spp, Adenovirus, Rotavirus, Astrovirus, Adenovirus (AdV), Norovirus, EIEC, EHEC, EAgEC, EPEC, ETEC,Clostridium difficile, Toxin A genes, Toxin B genes, Yersinia pseudotuberculosis, Yersinia enterocolitica, Y. enterocolitica virulence factor(attachment invasion locus Ail), Y. enterocolitica virulence factor(Yst enterotoxin), Y. enterocolitica virulence factor(plasmid pYV adhesin yadA)
3.250,00 د.إ
Gastro Intestinal(G.I) -Diarrheagenic E.coli Panel- 5 Parameters (Real Time PCR)- EIEC, EHEC, EAgEC, EPEC, ETEC
1.250,00 د.إ
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