Chlamydia trachomatis, ureaplasma urealyticum na mycoplasma genitalium

Nkọwa dị mkpirikpi:

A na-ezubere ngwa ahụ maka nchọpụta in vitro qualitative chlamydia trachomatis (CT), Ureaplasma urealyticum (UU), na Mycoplasma genitalium (MG) na nwoke urethral swab, nwanyị cervical swab, na nwanyi ikpu swab samples, na-enye aka na nchoputa na ọgwụgwọ nke genitourinary ọrịa.


Nkọwa ngwaahịa

Mkpado ngwaahịa

Aha ngwaahịa

HWTS-UR043-Chlamydia Trachomatis, Ureaplasma urealyticum na Mycoplasma genitalium Nucleic Acid Nchọpụta Ngwa

Epidemiology

Chlamydia trachomatis (CT) bụ ụdị prokaryotic microorganism nke na-akpachapụ anya parasitic na sel eukaryotic. Chlamydia trachomatis na-ekewa n'ime AK serotypes dịka usoro serotype siri dị. Ọrịa urogenital tract na-ebutekarị site na trachoma biological variant DK serotypes, na ụmụ nwoke na-egosipụtakarị dị ka urethritis, nke nwere ike ịkwụsị na-enweghị ọgwụgwọ, ma ọtụtụ n'ime ha na-aghọ nke na-adịghị ala ala, na-akawanye njọ mgbe ụfọdụ, a pụkwara ijikọta ya na epididymitis, proctitis, wdg. Enwere ike ịkpata ụmụ nwanyị na urethritis, salpingitis, nsogbu siri ike, wdg. Ureaplasma urealyticum (UU) bụ obere prokaryotic microorganism nke nwere ike ịdị ndụ n'adabereghị n'etiti nje bacteria na nje, ma bụrụkwa microorganism na-akpata ọrịa nke na-ebute ọrịa genital na urinary tract. Maka ụmụ nwoke, ọ nwere ike ịkpata prostatitis, urethritis, pyelonephritis, wdg. Maka ụmụ nwanyị, ọ nwere ike ịkpata mmeghachi omume mkpali na traktị ọmụmụ dịka vaginitis, cervicitis, na ọrịa pelvic inflammatory. Ọ bụ otu n'ime nje ndị na-akpata amụghị nwa na ite ime. Mycoplasma genitalium (MG) bụ ọrịa siri ike nke ukwuu ịzụlite, ọrịa na-ebute ngwa ngwa na-eto eto, ma bụrụ nke kacha nta nke mycoplasma [1]. Ogologo genome ya bụ naanị 580bp. Mycoplasma genitalium bụ ọrịa nje na-ebute site ná mmekọahụ nke na-ebute ọrịa traktị ọmụmụ dị ka urethritis na-abụghị gonococcal na epididymitis na ụmụ nwoke, cervicitis na ọrịa pelvic inflammatory na ụmụ nwanyị, na-ejikọta ya na ite ime na mberede na ịmụ nwa.

Nka nka

Nchekwa

-18 ℃

Ndụ nchekwa Ọnwa iri na abụọ
Ụdị ụdị nwoke urethral swab, nwanyị cervical swab, nwanyị ikpu swab.
Ct ≤38
CV 5.0%
LoD 400 oyiri/μL
Ngwa ndị ọdabara Ọdabara na ụdị I nchọpụta reagent:

Ngwa Biosystem 7500 ezigbo oge PCR,

QuantStudio®Sistemụ PCR 5 ezigbo oge, 

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

Sistemụ Nchọpụta PCR nke LineGene 9600 Plus (FQD-96A, Hangzhou Bioertechnology),

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

Sistemụ PCR nke BioRad CFX96,

BioRad CFX Opus 96 PCR ezigbo oge.

Ọdabara maka ụdị II reagent nchọpụta:

EudemonTMAIO800 (HWTS-EQ007) nke Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Usoro ọrụ

Macro & Micro-Test Viral DNA / RNA Kit (HWTS-3017) (nke enwere ike iji ya na Macro & Micro-Test Automatic Nucleic Acid Extractor (HWTS-3006C, HWTS-3006B)), na Macro & Micro-Test Viral DNA / RNA Kit (HWTS-3017-8 nwere ike iji E).TM AIO800 (HWTS-EQ007)) nke Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Ihe nlele nke ewepụtara bụ 200μL yana olu elution akwadoro bụ 150μL.


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