Chlamydia Trachomatis, Ureaplasma urealyticum and Mycoplasma genitalium

Short Description:

The kit is intended for the in vitro qualitative detection of Chlamydia trachomatis (CT), Ureaplasma urealyticum (UU), and Mycoplasma genitalium (MG) in male urethral swab, female cervical swab, and female vaginal swab samples, and provide aid to the diagnosis and treatment of patients with genitourinary tract infections.


Product Detail

Product Tags

Product name

HWTS-UR043-Chlamydia Trachomatis, Ureaplasma urealyticum and Mycoplasma genitalium Nucleic Acid Detection Kit

Epidemiology

Chlamydia trachomatis (CT) is a kind of prokaryotic microorganism that is strictly parasitic in eukaryotic cells. Chlamydia trachomatis is divided into A-K serotypes according to the serotype method. Urogenital tract infections are mostly caused by trachoma biological variant D-K serotypes, and males are mostly manifested as urethritis, which can be relieved without treatment, but most of them become chronic, periodically aggravated, and can be combined with epididymitis, proctitis, etc. Females can be caused with urethritis, cervicitis, etc., and more serious complications of salpingitis. Ureaplasma urealyticum (UU) is the smallest prokaryotic microorganism that can live independently between bacteria and viruses, and is also a pathogenic microorganism that is prone to genital and urinary tract infections. For men, it can cause prostatitis, urethritis, pyelonephritis, etc. For women, it can cause inflammatory reactions in the reproductive tract such as vaginitis, cervicitis, and pelvic inflammatory disease. It is one of the pathogens that cause infertility and abortion. Mycoplasma genitalium (MG) is an extremely difficult-to-cultivate, slow-growing sexually transmitted disease pathogen, and is the smallest type of mycoplasma [1]. Its genome length is only 580bp. Mycoplasma genitalium is a sexually transmitted infection pathogen that causes reproductive tract infections such as non-gonococcal urethritis and epididymitis in men, cervicitis and pelvic inflammatory disease in women, and is associated with spontaneous abortion and preterm birth.

Technical Parameters

Storage

-18℃

Shelf-life 12 months
Specimen Type male urethral swab,female cervical swab,female vaginal swab
Ct ≤38
CV <5.0%
LoD 400Copies/μL
Applicable Instruments Applicable to type I detection reagent:

Applied Biosystems 7500 Real-Time PCR Systems, 

QuantStudio®5 Real-Time PCR Systems, 

SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co., Ltd.),

LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, Hangzhou Bioertechnology), 

MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co., Ltd.),

BioRad CFX96 Real-Time PCR System,

BioRad CFX Opus 96 Real-Time PCR System.

Applicable to type II detection reagent:

EudemonTM AIO800 (HWTS-EQ007) by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Work Flow

Macro & Micro-Test Viral DNA/RNA Kit (HWTS-3017) (which can be used with Macro & Micro-Test Automatic Nucleic Acid Extractor (HWTS-3006C, HWTS-3006B)), and Macro & Micro-Test Viral DNA/RNA Kit (HWTS-3017-8) (which can be used with EudemonTM AIO800 (HWTS-EQ007)) by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

The extracted sample volume is 200μL and the recommended elution volume is 150μL.


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