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)


 
Uso previsto

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.

 

Información del pedido

ÁRBITRO Nombre del producto Tipo Tamaño del paquete
ST14021X Kit de detección multiplexada de STI de Cowingene - STI 3 Líquido 48 pruebas/kit

 

Especificación

Objetivo de detección

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

Almacenamiento

≤-20℃ durante 18 meses

LoD

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

Muestra validada

Vaginal swab、cervical swab、urethral swab, urine.

Instrumentos compatibles

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

 

Características de rendimiento

Reactividad cruzada

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.

Sustancias interferentes

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

Precisión

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

 

Reactivos de apoyo recomendados

ÁRBITRO Nombre del producto Proceso de dar un título Tamaño del paquete
CW03021Q Kit de recolección de muestras de Cowingene (auto-recolección vaginal) ESTE 1 test/kit
CW04021Q Kit de recolección de muestras de Cowingene (orina recolectada por el paciente) ESTE 1 test/kit
CW06021Z Reactivo diluyente de muestra de Cowingene  ESTE 10 mL/bottle
CW07023Q Sistema NATBox de Cowingene ESTE 1 Unit

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