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Screening test for Thrombophilic disease 7 mutations, code AC034
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The device provides reagents for the identification of the main gene mutations involved in thrombophilc diseases (Factor V R506Q, H1299R, Y1702C; Factor II G20210A; MTHFR C677T, A1298C; PAI-1 4G/5G), through the amplification of target sequences, reverse-hybridization and colour development. Venous thrombosis is among the most common cardiovascular diseases, affecting about 1 in every 1000 people each year. Thrombotic risk is determined both by environmental factors (age, surgery, pregnancy, oral contraception) and genetic predisposition.

  • Detection: RDB on Strip
  • Test: 25

Φόρμα Ενδιαφέροντος

Διεύθυνση: Kαισαρείας 6, 11527, Αθήνα  /  2ος Οροφος  /  Τηλ: 210 7754303 & 210 7756251  /  Φαξ: 210 7472725  /  Εmail: ndd@ndd.gr


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