Solution reagent kit WizDx™ CrystalMix

laboratoryfor PCRlyophilized

WizDx™ CrystalMix CA/GV/UP is an in vitro Multiplex real-time PCR kit to help single or simultaneous diagnosis of Candida albicans, Gardnerella vaginalis, and Ureaplasma parvum infections for the qualitative detection using a vaginal swab and urine specimens from patients. Overview Simple procedures for Treponema pallidum diagnosis with ready-to-use reagents that assure high specificity & sensitivity. Room temperature stable reagents with no need for cold chain logistics. Compatibility with various PCR systems: From mobile to laboratory use PCR systems. When using CLEO™ Q16, automatic result analysis can be linked with the LIS system and convenient results can be checked with the CLEO™ Q16 Viewer for PC. Kit Contents 96 tubes for the detection of CA/GV/UP (8 strip x 12 ea), Freeze-dried 1 vial, Positive Control 1 vial, Deionized sterile Water High sensitive Limit of detection (LoD) is 0.63 copies/pL for C. albicans and 1.25 copies/pL for G. vaginalis and U. parvum. Perfect Reproduciüility WizDx’" CrystalMix CA/GV/UP kits are precisely dispensed by fully automated dispensers in facilities certified with IS013485 and GMP. They are supplied in lyophilized form with a single test quantity, so all kits delrver exactly the same results. Prevent Carryover-contamination WizDx"* CrystalMix CA/GV/UP kit contains Uracil-DNA glycosy-lase (UDG) and dUTPs eliminating possible carryover contami-nation. High Specificity Accurate inspection is possible through the spécifie probedesign for the YST1 gene of Candida albicans. 23S gene of Gardnerella vaginlais and UreD gene of Ureaplasma.