Molecular Diagnostics of Acid Fast Bacteria by Polymerase Chain Reaction (MDx AFB Molecular ID PCR)
Mycobacterium tuberculosis and other acid-fast bacteria are causative agents of tuberculosis and atypical mycobacterial infections affecting lungs, gastrointestinal system, lymph nodes, skin, and many other organs. MDx AFB Molecular ID PCR is a molecular diagnostic test which helps healthcare professionals to detect and identify Mycobacterium tuberculosis complex and other Mycobacterium species in patient samples thereby […]
Molecular Diagnostics (MDx) Adenovirus Polymerase Chain Reaction (PCR)
Adenovirus is a common respiratory and gastrointestinal infection spreading through respiratory droplets, oral transmission, or contact, leading to mild respiratory illnesses, pneumonia, and gastroenteritis. MDx Adenovirus PCR is a molecular diagnostic test which helps healthcare providers detect adenovirus DNA utilizing PCR with specific primers and probes. The test is suggested for accurate diagnosis and timely […]
Molecular Diagnosis (MDx) Thrombotic Screen Polymerase Chain Reaction (PCR)
Thrombosis screening with PCR is a molecular genetic diagnostic test used by healthcare professionals to detect genetic mutations predisposing to thrombophilia, aggravating abnormal blood clotting within blood vessels and obstructing blood flow. This test is recommended for evaluating thrombophilia risk with venous thromboembolism, thrombosis, organ infarction and recurrent miscarriages. This test helps initiate thromboprophylaxis strategies, […]
MDx Beta-Thalassemia PCR
Beta thalassemia is a type of genetic disorder characterized by reduced beta chain synthesis hampering hemoglobin production. PCR assay uses targeted primers, which are amplified and used to identify mutant alleles. Healthcare professionals use the Molecular Diagnostics (MDx) Beta Thalassemia Polymerase Chain Reaction (PCR) test to diagnose and classify beta thalassemia, identify carriers, and facilitate […]
FISH Workup
The FISH (Fluorescence in situ hybridization) Workup identifies genetic abnormalities, facilitating more accurate patient diagnostics and tailored therapeutic matches. FISH detects sites of specific DNA sequences in metaphase or interphase cells. Healthcare practitioners utilize this test to pinpoint particular DNA sequences, diagnose genetic disorders, map genes, and identify novel oncogenes or genetic irregularities associated with […]
FISH Microdeletion Syndromes
The Fluorescence in Situ Hybridization (FISH) Microdeletion Syndromes test screens for microdeletion syndromes resulting from chromosomal deletions smaller than five megabases. These syndromes are associated with multiple congenital anomalies and developmental delays. Fluorescence in situ hybridization detects cryptic chromosomal rearrangements compared to traditional chromosome analysis. The test confirms screening results, screens family members, and performs […]
FLT3 ITD Mutation PCR results
The FMS-like tyrosine kinase-3 internal tandem duplication (FLT3-ITD) mutation is a mutation associated with acute myeloid leukemia (AML) in the FLT3 gene. Mutation occurs as internal tandem duplications (ITD) in the FLT3 gene, which is detected by a polymerase chain reaction (PCR) test that amplifies, analyzes DNA fragments, and identifies duplications. Identification of FLT3-ITD mutations […]
