This kit is intended for in vitro detection of Neisseria Gonorrhoeae(NG) nucleic acid in male urine, male urethral swab, female cervical swab samples.
Epidemiology
Gonorrhea is a classic sexually transmitted disease caused by infection with Neisseria gonorrhoeae (NG), which mainly manifests as purulent inflammation of the mucous membranes of the genitourinary system. NG can be divided into several ST types. NG can invade the genitourinary system and reproduce, causing urethritis in men, urethritis and cervicitis in women. If not treated thoroughly, it can spread to the reproductive system. The fetus can be infected through the birth canal resulting in neonatal gonorrhea acute conjunctivitis. Humans have no natural immunity to NG and are susceptible to NG. Individuals have weak immunity after infection which cannot prevent reinfection.
PCR Amplification Conditions Setting
Storage - Liquid:≤-18℃ In dark
Shelf-life - 12 months
Specimen Type - Male urethral secretions, Male urine, Female exocervical secretions
Ct - ≤38
CV - ≤5.0%
LoD - 50Copies/reaction
Specificity -
There is no cross-reactivity with other STD pathogens, such as Treponema pallidum, Chlamydia trachomatis, Ureaplasma urealyticum, Mycoplasma hominis, Mycoplasma genitalium and etc.
Applicable Instruments
It can match the mainstream fluorescent PCR instruments on the market.
Applied Biosystems 7500 Real-Time PCR Systems
Applied Biosystems 7500 Fast Real-Time PCR System
QuantStudio® 5 Real-Time PCR Systems
SLAN-96P Real-Time PCR Systems
LightCycler®480 Real-Time PCR system