I-Chlamydia Trachomatis, i-Ureaplasma Urealyticum ne-Neisseria Gonorrhoeae Nucleic Acid Detection Kit (i-Fluorescence PCR)

I-Chlamydia Trachomatis, i-Ureaplasma Urealyticum ne-Neisseria Gonorrhoeae Nucleic Acid Detection Kit (Fluorescence PCR) Isithombe Esifakiwe

Incazelo emfushane:

Le khithi ifanele ukutholwa kwekhwalithi yamagciwane avamile ezifweni ze-urogenital ku-vitro, okuhlanganisa i-Chlamydia trachomatis (CT), i-Ureaplasma urealyticum (UU), ne-Neisseria gonorrhoeae (NG).

Thumela i-imeyili kithi

Imininingwane Yomkhiqizo

Omaka bomkhiqizo

Igama Lomkhiqizo

I-HWTS-UR019A-I-Chlamydia Trachomatis eyomisiwe, i-Ureaplasma Urealyticum ne-Neisseria Gonorrhoeae Nucleic Acid Detection Kit (i-Fluorescence PCR)

HWTS-UR019D-Chlamydia Trachomatis, Ureaplasma Urealyticum and Neisseria Gonorrhoeae Nucleic Acid Detection Kit (Fluorescence PCR)

I-Epidemiology

Izifo ezithathelwana ngocansi (STD) zihlala zingenye yezinsongo ezinkulu ekuvikelekeni kwezempilo yomphakathi emhlabeni jikelele, okungaholela ekungazali, ukuzalwa kombungu ngaphambi kwesikhathi, i-tumorigenesis kanye nezinkinga ezinzima ezihlukahlukene.Kunezinhlobo eziningi zamagciwane e-STD, okuhlanganisa izinhlobo ezinjengamabhaktheriya, amagciwane, i-chlamydia, i-mycoplasma nama-spirochetes, njll., futhi izinhlobo ezivamile i-Neisseria gonorrhoeae, i-Chlamydia trachomatis, i-Ureaplasma urealyticum, i-Herpes simplex virus type 1, i-herpes simplex virus uhlobo 2, I-Mycoplasma hominis, i-Mycoplasma genitalium, njll.

Isiteshi

FAM	I-Chlamydia trachomatis (CT)
I-VIC(HEX)	I-Ureaplasma urealyticum (UU)
I-ROX	I-Neisseria gonorrhoeae (NG)
CY5	Ukulawula Kwangaphakathi

Imingcele Yezobuchwepheshe

Isitoreji	Uketshezi: ≤-18℃ ebumnyameni;I-Lyophilized: ≤30℃ ebumnyameni
Impilo yeshelufu	Izinyanga ezingu-12
Uhlobo lwesifanekiso	Ukukhishwa kwe-urethral, ukukhishwa komlomo wesibeletho
Ct	≤38
CV	≤5.0%
LoD	Uketshezi: Amakhophi angu-50/ukusabela;I-Lyophilized: 500Copies/mL
Ukucaciswa	Akukho ukuphinda kusebenze ukuze kutholwe amanye amagciwane atheleleke nge-STD, njenge-Treponema pallidum, njll.
Izinsimbi Ezisebenzayo	Ingakwazi ukufanisa amathuluzi e-PCR e-fluorescent avamile emakethe. I-Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR System I-QuantStudio® 5 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems Uhlelo lwe-PCR lwe-LightCycler®480 Real-Time LineGene 9600 Plus Real-Time PCR Uhlelo Lokuthola I-MA-6000 Real-Time Quantitative Thermal Cycler I-BioRad CFX96 Real-Time PCR System I-BioRad CFX Opus 96 Real-Time PCR System

Ukugeleza komsebenzi

Inketho 1.

Isisetshenziswa esisebenzayo sokukhipha esinconyiwe: I-Macro & Micro-Test Viral DNA/RNA Kit( HWTS-3001, HWTS-3004-32, HWTS-3004-48) kanye ne-Macro & Micro-Test Automatic Nucleic Acid Extractor(HWTS-3006).

Inketho yesi-2.

Isisetshenziswa esisebenzayo sokukhipha esinconyiwe: Isizinda se-Nucleic Acid noma i-Purification Reagent(YDP302) yi-Tiangen Biotech(Beijing) Co.,Ltd.

Okwedlule: I-STD Multiplex Detection Kit (Fluorescence PCR)

Olandelayo: I-Nucleic Acid Detection Kit esekelwe ku-Enzymatic Probe Isothermal Amplification (EPIA) ye-Group B Streptococcus

Bhala umyalezo wakho lapha futhi usithumelele wona