Showing 10–18 of 18 results
-
د.إ3,400.00
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.
-
د.إ1,050.00
Immunohistochemical (IHC) Stain tests are advanced diagnostic tools used to detect specific antigens in tissue samples, aiding in disease diagnosis, particularly cancer. These tests utilize highly specific antibodies to identify cellular markers, enabling precise differentiation between tissue types and disease states.
Sample Type : Paraffin Embedded Block/Charged Slides
Methodology : Immunohistochemical
TAT : 5 days
-
د.إ850.00
Sample Type : Serum
Methodology : Nephelometry
TAT : 10 Days
-
د.إ2,720.00
The Jak 2 Exon 12-15 Mutation Analysis is a specialized genetic test designed to detect mutations in exons 12-15 of the JAK2 gene, which are associated with myeloproliferative neoplasms (MPNs) such as polycythemia vera (PV) and other hematologic disorders. This test offers high sensitivity and specificity, enabling early and accurate diagnosis, which is crucial for targeted treatment decisions and disease monitoring. Unlike standard JAK2 V617F mutation tests, this analysis identifies rare but clinically significant mutations, providing comprehensive genetic profiling for patients with suspected MPNs. Its advanced molecular technology ensures reliable results, supporting personalized therapeutic strategies and improving patient outcomes.
-
د.إ745.00
Sample Type : Whole Blood
Methodology : Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)
TAT : 10 Days
-
د.إ1,450.00
Sample Type : Serum
Methodology : Enzyme-immunoassay
TAT : 10 Days
-
د.إ180.00
Sample Type : Plasma
Methodology : Spectrophotometry
TAT : 10 Days
-
د.إ3,750.00
The **Ros1 – Fish Test** is a highly sensitive and reliable fluorescence in situ hybridization (FISH) assay designed for the detection of **ROS1 gene rearrangements** in tumor samples. This test is crucial for identifying patients who may benefit from targeted therapies, particularly in **non-small cell lung cancer (NSCLC)**. Key features include **high specificity and accuracy**, rapid turnaround time, and **direct visualization of gene rearrangements** at the cellular level. Its benefits include **early and precise diagnosis**, enabling personalized treatment decisions and improving patient outcomes. The **unique selling point** of the Ros1 – Fish Test is its **proven clinical utility in guiding targeted therapy selection**, making it an essential tool for oncologists and pathologists in precision medicine.
-
د.إ90.00
Sample Type : Serum
Methodology : Spectrophotometry
TAT : 1 Day
