Mycoplasma hominis, Ureaplasma urealyticum na Gardnerella vaginalis nucleic acid.
Aha ngwaahịa
HWTS-UR044-Mycoplasma hominis, Ureaplasma urealyticum na Gardnerella vaginalis Nucleic Acid Detection Kit (Fluorescence PCR)
Epidemiology
Mycoplasma hominis (MH) bụ ụdị mycoplasma nke dị na eriri afọ urinary na akụkụ ahụ ma nwee ike ibute ọrịa urinary tract na mbufụt. Mycoplasma hominis bụ n'ọtụtụ ebe na ọdịdị na-ejikọta ya na a dịgasị iche iche nke genitourinary tract ọrịa dị ka nongonococcal urethritis, nwanyi cervicitis, adnexitis, infertility, wdg Ureaplasma urealyticum (UU) bụ kasị nta prokaryotic celled microorganism na n'etiti nje bacteria na nje na ọ nwere ike na-ebi ndụ n'ụzọ dị mfe a urinary tract na microorganism. ọrịa traktị. Maka ụmụ nwoke, ọ nwere ike ịkpata prostatitis, urethritis, pyelonephritis, wdg; maka ụmụ nwanyị, ọ nwere ike ịkpata mmeghachi omume mkpasu iwe na traktị ọmụmụ dị ka vaginitis, cervicitis, na ọrịa pelvic inflammatory, ma bụrụ otu n'ime ihe ndị na-akpata enweghị ọmụmụ na ime ọpụpụ. Ihe na-ebutekarị vaginitis na ụmụ nwanyị bụ nje vaginosis, na nje bacteria dị mkpa nke nje vaginosis bụ Gardnerella vaginalis. Gardnerella vaginalis (GV) bụ nje na-akpata ohere nke na-adịghị ebute ọrịa mgbe ọ dị obere. Otú ọ dị, mgbe a na-ebelata ma ọ bụ kpochapụ nje bacteria Lactobacilli kasịnụ, na-eme ka ahụ ghara ịdị na mpaghara ikpu, Gardnerella vaginalis na-amụba n'ọtụtụ buru ibu, na-eduga na vaginosis nje. N'otu oge ahụ, nje ndị ọzọ (dị ka Candida, Neisseria gonorrhoeae, Mycoplasma hominis, wdg) nwere ike ịwakpo ahụ mmadụ, na-ebute vaginitis na cervicitis agwakọta. Ọ bụrụ na achọpụtaghị vaginitis na cervicitis ma gwọọ ya n'oge na nke dị irè, enwere ike inwe ọrịa na-arị elu site na nje ndị na-efe efe n'akụkụ mucosa nke ịmụ nwa, na-eduga n'ụzọ dị mfe na ọrịa traktị dị elu dị ka endometritis, salpingitis, tubo-ovarian abscess (TOA), na pelvic peritonitis, nke nwere ike ịkpata nsogbu dị njọ na ọbụna ime ime.
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 | UU, GV 400Copy/ml; MH 1000 oyiri/ml |
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.), LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, teknụzụ Hangzhou Bioer), 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.