Cowingene STI Multiplex Detection Kit-STI 7(Lyophilized)

REF: ST13022U Validated Specimen: vaginal swab、cervical swab、urethral swab, urine. Analytes:2 tubes:CT、NG、MH、MG、UU、UP、TV

Cowingene STI Multiplex Detection Kit-STI 7(Lyophilized)


 
Utilizare intenționată

The Cowingene STI Multiplex Detection Kit (STI Detection Kit) is intended for the in vitro qualitative detection of multiplex sexually transmitted infection pathogens, and provides aid to the diagnosis and treatment of patients with genitourinary tract infections. Sexually transmitted infection (STI) remains one of the important threats to global public health security. The disease can lead to infertility, premature birth, tumors and various serious complications. There are many types of STI pathogens, including bacteria, viruses, chlamydia, mycoplasma and spirochetes, etc. Common species include Chlamydia trachomatis, Ureaplasma urealyticum, Ureaplasma parvum,Mycoplasma hominis, Herpes simplex virus type 1, Neisseria gonorrhoeae, Herpes simplex virus type 2, Mycoplasma genitalium, Candida albicans, Treponema pallidum,Gardnerella vaginalis, Trichomonas vaginalis, etc.
This kit (STI 7 Detection Kit) is intended for the in vitro qualitative detection of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh),Ureaplasma urealyticum (UU), Ureaplasma parvum (UP), Mycoplasma genitalium (Mg) and Trichomonal vaginitis (TV) in urine, male urethral swab, female cervical swab, and female vaginal swab samples, and provides aid to the diagnosis and treatment of patients with genitourinary tract infections.

 

Informații despre comandă

REF Nume produs Tip Dimensiunea pachetului
ST13022U Cowingene STI Multiplex Detection Kit-STI 7 Lyophilize 16 teste/kit

 

Specificații

Țintă de detectare

hlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh),Ureaplasma urealyticum (UU), Ureaplasma parvum (UP), Mycoplasma genitalium (Mg) and Trichomonal vaginitis (TV)

Depozitare

2-30℃ timp de 18 luni

Nivel de detaliere (LoD)

The LoD of the kit for detecting CT, NG, Mh, UU,UP, Mg and TV is 400Copies/mL

Specimen validat

Female vaginal swab,Female cervical swab,Male urethral swab,Urine

Instrumente compatibile

Aparat PCR în timp real deschis cu canale FAM, VIC/HEX, ROX, CY5, adică ABI 7500, Roche 480, Bio-Rad CFX96 etc.

 

Caracteristici de performanță

Reactivitate încrucișată

There is no cross-reactivity with high-risk HPV (16/18), Staphylococcus epidermidis/Staphylococcus saprophyticus, Escherichia coli, Lactobacillus crispatus, Prevotella,Adenovirus, Cytomegalovirus, Herpes simplex virus I/II, Candida albicans, Gardnerella vaginalis, Group B Streptococcus, Haemophilus ducreyi, Treponema pallidum, Human immunodeficiency virus, Lactobacillus casei and human genomic DNA.

Substanțe interferente

The results show that when the samples contain blood, cervical mucus, 60mg/L of clindamycin suppository,vaginal lubricant, 60mg/mL of mucin and 40mg/L of amphotericin, there is no impact on the test results of the kit.

Precizie

The %CV of repeatability (within-lot) and reproducibility (inter-lot, day, run, operators and labs) are all ≤5.0% of CT, NG, Mh, UU, UP, Mg and TV target

 

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