Risultati per factor II genetic analysis test kit

Di seguito l'elenco dei risultati di ricerca trovati rilevanti per la keyword 'factor II genetic analysis test kit':

Risultati maggiormente rilevanti:

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 cobas® ️factor ii and factor v test - roche diagnostics usa
Intended use. The cobas® Factor II and Factor V Test is an in vitro diagnostic device that uses real-time Polymerase Chain Reaction (PCR) for the detection and genotyping of the human Factor II (Prothrombin) G20210A mutation and the human Factor V Leiden G1691A mutation, from genomic DNA obtained from K2EDTA whole blood specimens, as an aid in ...

 cepheid | factor ii and factor v molecular test - xpert fii & fv
Xpert ® FII & FV is a qualitative genotyping test for the fast detection of Factor II and Factor V alleles. Performed on the Cepheid GeneXpert System, the test is intended to provide rapid results for Factor II mutation c.*97G>A (formally 20210G>A) and Factor V Leiden c.1601G>A (R506Q) mutations as an aid in the diagnosis of suspected thrombophilia.

 cepheid | factor ii and factor v molecular test - xpert fii & fv
Xpert ® FII & FV is a qualitative genotyping test for the rapid detection of Factor II (FII) and Factor V (FV) alleles. Performed on the Cepheid GeneXpert System, the test is intended to provide rapid results for FII (G20210A) and FV Leiden (G1691A) mutations as an aid in the diagnosis of suspected thrombophilia.

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 511162: factor ii (prothrombin), dna analysis | labcorp
The c.*97G>A variant in the F2 gene is a genetic risk factor for venous thromboembolism. Heterozygous carriers have a 2- to 4-fold increased risk for venous thromboembolism. Homozygotes for the c.*97G>A variant are rare. The annual risk of VTE in homozygotes has been reported to be 1.1% per year. Individuals who carry both a *97G>A variant in ...

 risultati per factor ii genetic analysis test kit
hpsc genetic analysis kit - stemcell This qPCR-based kit enables the genetic screening of multiple hPSC lines and contains enough material to analyze 20 individual samples in triplicate. It uses double-quenched probes with a 5-carboxyfluorescein (5-FAM) dye to give superior performance over other, single-quenched probes.

 factor ii (prothrombin), dna analysis - labcorp
The c.*97G>A variant in the F2 gene is a genetic risk factor for venous thromboembolism. Heterozygous carriers have a 2- to 4-fold increased risk for venous thromboembolism. Homozygotes for the c.*97G>A variant are rare. The annual risk of VTE in homozygotes has been reported to be 1.1% per year. Individuals who carry both a *97G>A variant in ...

 prothrombin (factor ii) g20210a genotyping - clinical test - nih ...
Clinical Molecular Genetics test for Thrombophilia and using Targeted variant analysis, PCR offered by Molecular Diagnosis Centre. There are links to the lab to order the test and links to practice guidelines and authoritative resources like GeneReviews, PubMed, MedlinePlus, PharmGKB to support the clinician's informed test selection.

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