Cowingene STI Multiplex Detection Kit-STI 3(Liquid)

REF: ST14021X Validated Specimen: vaginal swab、cervical swab、urethral swab, urine. Analytes: 1 tube:CT、NG、TV

Cowingene STI Multiplex Detection Kit-STI 3 (Liquid)


 
Verwendungszweck

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 is intended for the in vitro qualitative detection of Chlamydia trachomatis (CT),Neisseria gonorrhoeae (NG), 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.

 

Bestellinformationen

Referenz Produktname Typ Paketgröße
ST14021X Cowingene STI Multiplex Detection Kit-STI 3 Flüssig 48 Tests/Kit

 

Spezifikation

Erkennungsziel

Chlamydia trachomatis (CT),Neisseria gonorrhoeae (NG), Trichomonal vaginitis (TV)

Lagerung

≤-20℃ für 18 Monate

LoD

The LoD of the kit for detecting CT, NG and TV is 400 copies/mL

Validierte Probe

Vaginal swab、cervical swab、urethral swab, urine.

Kompatible Instrumente

Open real time PCR machine with channels FAM, VIC/HEX, ROX, CY5, i.e. ABI 7500, Roche 480, Bio-Rad CFX96, etc

 

Leistungsmerkmale

Kreuzreaktivität

There is no cross-reactivity between this kit and other genitourinary tract infection pathogens such as high-risk Human papillomavirus type 16, Human papillomavirus type 18, Herpes simplex virus type Ⅱ, Treponema pallidum,Ureaplasma urealyticum, Mycoplasma hominis, Mycoplasma genitalium,Staphylococcus epidermidis, Escherichia coli, Gardnerella vaginalis, Candida albicans,Lactobacillus crispatus, Adenovirus,Cytomegalovirus, Group B Streptococcus, Human immunodeficiency virus, Lactobacillus casei and human genomic DNA, etc.

Störende Substanzen

The interfering samples which contain bilirubin (0.2mg/mL),cervical mucus (10%), white blood cells (109 cells/mL), mucin (60mg/mL), whole blood (10%), semen (10%), levofloxacin (0.2mg/mL), erythromycin (0.3mg/mL),penicillin (0.5mg/mL), azithromycin (0.3mg/mL), Jieryin lotion (10%), Fuyanjie lotion (10%) will not affect the test results

Präzision

The %CV of repeatability and reproducibility are all ≤5.0% of CT, NG and TV target.

 

Empfohlene unterstützende Reagenzien

Referenz Produktname Zertifizierung Paketgröße
CW03021Q Cowingene-Probenentnahmeset (selbst entnommene Vaginalprobe) DAS 1 test/kit
CW04021Q Cowingene-Probenentnahmeset (selbst gesammelter Urin) DAS 1 test/kit
CW06021Z Cowingene-Probenverdünnungsreagenz  DAS 10 mL/bottle
CW07023Q Cowingene NATBox-System DAS 1 Unit

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