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)


 
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 (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.

 

Información del pedido

ÁRBITRO Nombre del producto Tipo Tamaño del paquete
ST13022U Cowingene STI Multiplex Detection Kit-STI 7 Lyophilize 16 pruebas/kit

 

Especificación

Objetivo de detección

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

Almacenamiento

2-30℃ durante 18 meses

LoD

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

Muestra validada

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

Instrumentos compatibles

Máquina de PCR en tiempo real abierta con canales FAM, VIC/HEX, ROX, CY5, es decir, ABI 7500, Roche 480, Bio-Rad CFX96, etc.

 

Características de rendimiento

Reactividad cruzada

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.

Sustancias interferentes

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.

Precisión

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

 

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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