Testsea Disease Test I-HIV 1/2 Rapid Test Kit
Imininingwane Esheshayo
I gama le-brand: | Testsea | Igama lomkhiqizo: | HIV 1/2 Isivivinyo |
Indawo Yomsuka: | I-Zhejiang, China | Uhlobo: | Izinsiza Zokuhlaziya I-Pathological |
Isitifiketi: | ISO9001/ISO13485 | Ukuhlukaniswa kwezinsimbi | Ikilasi III |
Ukunemba: | 99.6% | Isifanekiso: | Igazi Eliphelele/iSerum/Plasma |
Ifomethi: | I-Cassette | Ukucaciswa: | 3.00mm/4.00mm |
I-MOQ: | 1000 Pcs | Impilo yeshelufu: | iminyaka engu-2 |
OEM & ODM | ukusekela | Ukucaciswa: | 40ama-pcs/ibhokisi |
Ikhono Lokuhlinzeka:
5000000 Ucezu/Izingcezu Ngenyanga
Ukupakisha nokulethwa:
Imininingwane yokupakisha
40pcs/ibhokisi
2000PCS/CTN, 66*36*56.5cm, 18.5KG
Isikhathi esiholayo:
Ubuningi(izingcezu) | 1 - 1000 | 1001 - 10000 | > 10000 |
Isikhathi sokuhola (izinsuku) | 7 | 30 | Kuzoxoxiswana |
Incazelo Yevidiyo
Ukusetshenziswa Okuhlosiwe
Ukuhlolwa kwe-One Step HIV(1&2) kuyisivivinyo se-chromatographic immunoassay ukuze kutholwe ikhwalithi yamasosha omzimba ku-human immunodeficiency virus (HIV) ku-Whole Blood / Serum / Plasma ukusiza ekuxilongweni kwe-HIV.
Isifinyezo
I-human immunodeficiency virus (HIV) igciwane lesandulela ngculazi elihlasela amangqamuzana amasosha omzimba, licekele phansi noma liphazamise ukusebenza kwawo.Njengoba ukutheleleka kuqhubeka, isimiso somzimba sokuzivikela ezifweni siba buthakathaka, futhi umuntu uba sengozini yokuthola izifo.Isigaba esithuthuke kakhulu sokutheleleka nge-HIV yi-acquired immunodeficiency syndrome (AIDS).Kungathatha iminyaka eyi-10-15 ukuthi umuntu one-HIV abe nesifo sengculazi.Indlela ejwayelekile yokuthola ukuthi usuleleke nge-HIV wukubheka ubukhona bamasosha omzimba egciwaneni ngendlela ye-EIA elandelwa wukuqinisekisa nge-Western.
Inqubo Yokuhlola
Vumela ukuhlola, isifanekiso, isigcinalwazi kanye/noma izilawuli ukuthi zifinyelele izinga lokushisa legumbi elingu-15-30℃ (59-86℉) ngaphambi kokuhlolwa.
1. Letha isikhwama ekamelweni lokushisa ngaphambi kokusivula.Susa idivayisi yokuhlola esikhwameni esivaliwe futhi uyisebenzise ngokushesha.
2. Beka idivayisi yokuhlola endaweni ehlanzekile neleveli.
3. Ngeserum noma isampula se-plasma: Bamba i-dropper ngokuqondile bese udlulisela amaconsi angu-3 e-serum noma i-plasma (cishe u-100μl) esibonelweni somthombo(S) wensiza yokuhlola, bese uqala isibali sikhathi.Bheka umfanekiso ngezansi.
4. Ngezibonelo zegazi eliphelele: Bamba i-dropper ngokuqondile bese udlulisela iconsi elingu-1 legazi eliphelele (cishe u-35μl) esibonelweni somthombo(S) wedivayisi yokuhlola, bese wengeza amaconsi angu-2 ebhafa (cishe u-70μl) bese uqala isibali sikhathi.Bheka umfanekiso ngezansi.
5. Linda kuze kuvele i(ama)layini anombala.Funda imiphumela ngemizuzu eyi-15.Ungahumushi umphumela ngemuva kwemizuzu engama-20.
Ukusebenzisa inani elanele lesifanekiso kubalulekile ukuze uthole umphumela wokuhlola ovumelekile.Uma ukufuduka (ukumanziswa kolwelwesi) kungabonakali efasiteleni lokuhlola ngemva komzuzu owodwa, engeza ithonsi elilodwa ngaphezulu le-buffer (yegazi eliphelele) noma isifanekiso (seserum noma i-plasma) esibonelweni kahle.
Ukuhunyushwa Kwemiphumela
Okuhle:Kuvela imigqa emibili.Umugqa owodwa kufanele uvele njalo endaweni yomugqa wokulawula(C), futhi omunye ulayini obonakalayo onombala kufanele uvele endaweni yomugqa wokuhlola.
Okubi:Umugqa owodwa onombala uvela endaweni yokulawula(C).Awukho umugqa onombala ovela endaweni yomugqa wokuhlola.
Okungavumelekile:Ulayini wokulawula uyehluleka ukuvela.Ivolumu yesampula enganele noma izindlela zenqubo ezingalungile yizona zizathu okungenzeka kakhulu zokwehluleka komugqa wokulawula.
★ Buyekeza inqubo bese uphinda ukuhlolwa ngedivayisi entsha yokuhlola.Uma inkinga iqhubeka, yeka ukusebenzisa ikhithi yokuhlola ngokushesha futhi uxhumane nomsabalalisi wangakini.
★ Buyekeza inqubo bese uphinda ukuhlolwa ngedivayisi entsha yokuhlola.Uma inkinga iqhubeka, yeka ukusebenzisa ikhithi yokuhlola ngokushesha futhi uxhumane nomsabalalisi wangakini.
Uhlu Lomkhiqizo
Igama lomkhiqizo | Isifanekiso | Ifomethi | Isitifiketi |
I-Influenza Ag A Test | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
Ukuhlolwa komkhuhlane we-Ag B | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
I-HCV Hepatitis C Virus Ab Test | I-WB/S/P | Ikhasethi | ISO |
I-HIV 1+2 Test | I-WB/S/P | Ikhasethi | ISO |
HIV 1/2 Tri-line Test | I-WB/S/P | Ikhasethi | ISO |
Ukuhlolwa kwe-HIV 1/2/O Amasosha omzimba | I-WB/S/P | Ikhasethi | ISO |
Ukuhlolwa kweDengue IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Dengue NS1 Antigen | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Dengue IgG/IgM/NS1 Antigen | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-H.Pylori Ab | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-H.Pylori Ag | Indle | Ikhasethi | CE ISO |
I-Syphilis (Anti-treponemia Pallidum) Ukuhlolwa | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kweTyphoid IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Toxo IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa Kwesifo Sofuba | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa Okusheshayo kwe-HBsAg | I-WB/S/P | Ikhasethi | ISO |
Ukuhlolwa Okusheshayo kwe-HBsAb | I-WB/S/P | Ikhasethi | ISO |
Isivivinyo Esisheshayo se-HBeAg | I-WB/S/P | Ikhasethi | ISO |
Isivivinyo Esisheshayo se-HBeAb | I-WB/S/P | Ikhasethi | ISO |
Ukuhlolwa Okusheshayo kwe-HBcAb | I-WB/S/P | Ikhasethi | ISO |
Ukuhlolwa kwe-Rotavirus | Indle | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Adenovirus | Indle | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Norovirus Antigen | Indle | Ikhasethi | ISO |
I-HAV Hepatitis A virus Test IgM | I-WB/S/P | Ikhasethi | ISO |
I-HAV Hepatitis A virus Test IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
I-Malaria Ag pf/pv Ukuhlolwa kwe-Tri-line | WB | Ikhasethi | CE ISO |
I-Malaria Ag pf/pan Tri-line Test | WB | Ikhasethi | ISO |
Umalaleveva Ab pf/pv Ukuhlolwa Kwemigqa Emithathu | WB | Ikhasethi | CE ISO |
I-Malaria Ag pv Test | WB | Ikhasethi | CE ISO |
I-Malaria Ag pf Test | WB | Ikhasethi | CE ISO |
Umalaleveva Ag pan Test | WB | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Leishmania IgG/IgM | I-Serum/Plasma | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Leptospira IgG/IgM | I-Serum/Plasma | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Brucellosis(Brucella)IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Chikungunya IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Chlamydia trachomatis Ag | I-Endocervical Swab/Urethral swab | Ikhasethi | ISO |
Ukuhlolwa kwe-Neisseria Gonorrhoeae Ag | I-Endocervical Swab/Urethral swab | Ikhasethi | CE ISO |
I-Chlamydia Pneumoniae Ab IgG/IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
I-Chlamydia Pneumoniae Ab IgM Test | I-WB/S/P | Ikhasethi | ISO |
I-Mycoplasma Pneumoniae Ab IgG/IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
I-Mycoplasma Pneumoniae Ab IgM Test | I-WB/S/P | Ikhasethi | CE ISO |
I-Rubella virus Test Ab IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Cytomegalo virus Antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
I-Herpes simplex virus Ⅰ ukuhlolwa kwe-antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
I-Herpes simplex virus Ⅱ i-antibody IgG/IgM test | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Zika virus antibody IgG/IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa kwe-Hepatitis E virus antibody IgM | I-WB/S/P | Ikhasethi | CE ISO |
Ukuhlolwa komkhuhlane we-Ag A+B | I-Nasopharyngeal Swab | Ikhasethi | CE ISO |
I-HCV/HIV/SYP Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
I-MCT HBsAg/HCV/HIV Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
I-HBsAg/HCV/HIV/SYP Multi Combo Test | I-WB/S/P | Ikhasethi | ISO |
Ikhasethi Lokuhlola I-Monkey Pox Antigen | I-Oropharyngeal swab | Ikhasethi | CE ISO |
Imikhiqizo Ehlobene
Ulwazi Lombukiso
Isitifiketi Sokuhlonishwa
Iphrofayela Yenkampani
Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokushesha yobuchwephesha be-biotechnology ekhethekile ekucwaningeni, ekuthuthukiseni, ekukhiqizeni nasekusabalaliseni amakhithi okuhlola e-in-vitro diagnostic(IVD) athuthukile namathuluzi ezokwelapha.
Indawo yethu yi-GMP, ISO9001, kanye ne-ISO13458 futhi sinemvume ye-CE FDA.Manje sesibheke ngabomvu ukubambisana nezinye izinkampani zaphesheya kwezilwandle ukuze sithuthukiselane.
Sikhiqiza ukuhlolwa kwenzalo, ukuhlolwa kwezifo ezithathelwanayo, ukuhlola ukusetshenziswa kabi kwezidakamizwa, ukuhlola umaka wenhliziyo, ukuhlolwa komaka isimila, ukuhlolwa kokudla nokuphepha kanye nokuhlolwa kwezifo zezilwane, ngaphezu kwalokho, uhlobo lwethu lwe-TESTSEALABS lwaziwa kakhulu ezimakethe zasekhaya neziphesheya kwezilwandle.Izinga eliphezulu nezintengo ezivumayo zisenza sikwazi ukuthatha amasheya asekhaya angaphezu kuka-50%.
OUKUPAKASHA NOKUTHUMELA
FAQ
Sizinze eZhejiang, eChina, siqala ngo-2015, sidayisela eNingizimu-mpumalanga ye-Asia (15.00%), Imakethe Yasekhaya (15.00%), eNingizimu, eMelika (10.00%), i-Afrika (10.00%), eNyakatho Melika (5.00%), eMpumalanga
IYurophu(5.00%),Oceania(5.00%),Mid East(5.00%),Eastern Asia(5.00%),Western Europe(5.00%),Central America(5.00%),Northern Europe(5.00%),Southern Europe( 5.00%),iNingizimu Asia(5.00%).Kukhona abantu abangaba ngu-51-100 ehhovisi lethu.
Njalo isampula yangaphambi kokukhiqiza ngaphambi kokukhiqizwa ngobuningi;
Ukuhlolwa kokugcina njalo ngaphambi kokuthunyelwa;
Ukuhlolwa Okusheshayo Kwezilwane, Amakhithi Okuhlola Inzalo, Amakhithi Okuhlola Izidakamizwa, Amakhithi Okuhlola Izifo Ezithathelwanayo, Ukuhlola Omaka Amathumba, Ukuhlolwa Kokuphepha Kokudla
Amandla acebile kwezobuchwepheshe, imishini ethuthukisiwe, uhlelo lokuphatha lwesimanje, uhla oluphelele lwezinsiza zokuhlola ngokushesha zokuxilongwa komtholampilo, komndeni kanye nelebhu, ISO, CE FSC eqinisekisiwe.
Imibandela Yokulethwa Eyamukelwe: FOB, CIF, EXW, FCA, DDP, Express Delivery;
Imali Yenkokhelo Eyamukelwayo: USD;RMB
Uhlobo Lwenkokhelo olwamukelwe: T/T, Western Union,Escrow;
Ulimi olukhulunywayo: IsiNgisi