Intended UseThis diagnostic kit is an in vitro nucleic acid(NA) amplification test to detect the presence of both Chlamydia Trachomatis(CT) and Neisseria Gonorrhoeae(NG) with male urethral swab or fem...
Intended Use
This diagnostic kit is an in vitro nucleic acid(NA) amplification test to detect the presence of both Chlamydia Trachomatis(CT) and Neisseria Gonorrhoeae(NG) with male urethral swab or female vagina/cervical swab.
Features
Methodology | Magnetic bead method |
Sample volume | 40ul |
Sample type | male urethral swab and female vagina and cervical swab |
Subtype coverage | CT subtype D,E,F,G,J, NG subtype WI, WII/WIII |
Linear range | CT:1.0E+02~1.0E+09 cfu/ml NG:1.0E+02~1.0E+09 cfu/ml |
Sensitivity | CT:100 IU/ml; NG:100 IU/ml |
