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IVD Product License No: 12-1805
(Korea MFDS)
Real-Q Factor II(prothrombin)
G20210A Kit
IVD Product License No: 12-1806
(Korea MFDS)
Real-Q Factor V Leiden(G1691A) Kit
IVD Product License No: 12-1807
(Korea MFDS)
Real-Q MTHFR Kit
IVD Product License No: 17-955
(Korea MFDS)
Real-Q RNF213 R4810K Kit

IVD Product License No: 12-1805 (Korea MFDS)

Real-Q Factor II(prothrombin) G20210A Kit

Intended Use

Real-Q Factor II (prothrombin) G20210A Kit is an in vitro diagnostic device for qualitative detection of the prothrombin gene mutation (G20210A) using real-time PCR from DNA extracted from human whole blood

Product Features

Specimen Type

Whole blood

Compatible Instruments

Result

Amplification curve (wild sample DNA)
Amplification curve (mutant sample DNA)
Amplification curve (hetero sample DNA)

IVD Product License No: 12-1806 (Korea MFDS)

Real-Q Factor V Leiden(G1691A) Kit

Intended Use

Real-Q Factor V Leiden (G1691A) Kit is an in vitro diagnostic medical device designed for qualitative detection of the Factor V Leiden (G1691A) mutation using real-time PCR from DNA extracted human whole blood

Product Features

Specimen Type

Whole blood

Compatible Instruments

Result

Amplification curve (wild sample DNA)
Amplification curve (mutant sample DNA)
Amplification curve (hetero sample DNA)

IVD Product License No.: 12-1807 (Korea MFDS)

Real-Q MTHFR(C677T, A1298C) Kit

Intended Use

Real-Q MTHFR (C677T, A1298C) Kit is an in vitro diagnostic device for qualitative detection of mutations at positions 677 and 1298 in the methylenetetrahydrofolate reductase (MTHFR) gene using real-time PCR from DNA extracted from human whole blood

Product Features

Specimen Type

Whole blood

Compatible Instruments

Result

Amplification curve (wild sample DNA)
Amplification curve (mutant sample DNA)
Amplification curve (hetero sample DNA)

IVD Product License No: 17-955 (Korea MFDS)

Real-Q RNF213 R4810K Kit

Intended Use

Real-Q RNF213 R4810K Kit is an in vitro diagnostic device that qualitatively detects the RNF213 (p.R4810K) mutation using real-time PCR from DNA extracted from blood specimens of patients or family members diagnosed with definite, unilateral, or probable Moyamoya disease, aiding molecular genetic diagnosis

Product Features

Specimen Type

Whole blood

Compatible Instruments

Result

Amplification curve (wild sample DNA)
Amplification curve (mutant sample DNA)
Amplification curve (hetero sample DNA)