Showing 41 – 60 out of 173
Page 3 out of 9
| Tick | Thumbnails | Products | Price | Quantity | Action |
|---|---|---|---|---|---|
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2.400,00 د.إ | ||||
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Cystic Fibrosis Single Mutation Sample Type : Whole Blood
Methodology : Gene amplification – inverse hybridisation (Innolipa)
TAT : 10 Days |
2.150,00 د.إ | |||
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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 The Cytomegalovirus (CMV) PCR Test from Lab Tests Dubai is a highly sensitive molecular diagnostic test that detects CMV DNA in your blood, giving you definitive proof of active infection, not just past exposure. |
1.050,00 د.إ | |||
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2.200,00 د.إ | ||||
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5.900,00 د.إ | ||||
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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 | |||
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1.520,00 د.إ | ||||
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1.600,00 د.إ | ||||
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1.520,00 د.إ | ||||
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5.500,00 د.إ | ||||
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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 | |||
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2.800,00 د.إ | ||||
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Gastro Intestinal(G.I) -Clostridium difficile + ToxA + ToxB Panel- 3 Parameters (Real Time PCR)- Clostridium difficile, Toxin A genes, Toxin B genes Sample Type : Stool
Methodology : PCR
TAT : 3 Day |
750,00 د.إ | |||
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3.250,00 د.إ | ||||
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Gastro Intestinal(G.I) -Diarrheagenic E.coli Panel- 5 Parameters (Real Time PCR)- EIEC, EHEC, EAgEC, EPEC, ETEC Sample Type : Stool
Methodology : PCR
TAT : 3 Day |
1.250,00 د.إ | |||
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Gastro Intestinal(G.I) -Yersinia Panel- 5 Parameters (Real Time PCR)- , 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) Sample Type : Stool
Methodology : PCR
TAT : 3 Day |
1.250,00 د.إ |