I-Dengue IgM/IgG/NS1 Antigen Test Test Dengue Combo Test
Isingeniso Esifushane
Udenga lusakazwa ngokulunywa umiyane i-Aedes onegciwane elilodwa kwamane amagciwane odenga. Kwenzeka ezindaweni ezishisayo nezishisayo emhlabeni. Izimpawu zivela ezinsukwini ezi-3-14 ngemuva kokulunywa okuthelelekile. I-Dengue fever yisifo esibuhlungu esihlasela izinsana, izingane ezincane kanye nabantu abadala. Umkhuhlane we-dengue hemorrhagic fever (umkhuhlane, ubuhlungu besisu, ukuhlanza, ukopha) yisifo esingase sibe yingozi, esihlasela kakhulu izingane. Ukuxilongwa kusenesikhathi kanye nokuphathwa komtholampilo ngokucophelela ngodokotela abanolwazi nabahlengikazi kwandisa ukusinda kweziguli. I-Dengue NS1 Ag-IgG/IgM Combo Test iwukuhlola okulula, okubonakalayo kwekhwalithi okuthola amasosha omzimba wegciwane lodenga kanye ne-antigen yegciwane lodenga I-NS1 antigen egazini lomuntu Lonke/i-serum/plasma. Ukuhlolwa kusekelwe ku-immunochromatography futhi kunganikeza umphumela phakathi nemizuzu engu-15.
Ulwazi Oluyisisekelo.
| Imodeli No | 101012 | Izinga Lokushisa Lokugcina | 2-30 degrees |
| I-Shelf Life | 24M | Isikhathi sokuthumela | Wezinsukwini eziyisi-7 zokusebenza |
| Ithagethi yokuxilonga | Dengue IgG IgM NS1 Virus | Inkokhelo | T/T Western Union Paypal |
| Iphakheji Yezokuthutha | Ikhathoni | Iyunithi yokupakisha | 1 Idivayisi yokuhlola x 10/ikhithi |
| Umsuka | China | Ikhodi ye-HS | 38220010000 |
Izinto Ezinikeziwe
1.Idivayisi yokuhlola ye-Testselabs iyodwa efakwe i-foil ene-desiccant
2.Isixazululo se-Assay ebhodleleni lokuwisa
3.Imanuwali yokufundisa ukuze isetshenziswe
Isici
1. Ukusebenza okulula
2. Umphumela ofundeka ngokushesha
3. Ukuzwela Okuphezulu nokunemba
4. Intengo enengqondo kanye nekhwalithi ephezulu
Ukuqoqwa Nokulungiswa Kwezifanekiso
1.I-Dengue NS1 Ag-IgG/IgM Combo Test ingenziwa ku-Whole Blood/Serum/Plasma.
2.Ukuqoqa igazi eliphelele, i-serum noma i-plasma specimens ngokulandela izinqubo zaselabhorethri zomtholampilo ezivamile.
3.Ukuhlola kufanele kwenziwe ngokushesha ngemva kokuqoqwa kwesifanekiso. Ungashiyi ama-specimens ekamelweni lokushisa isikhathi eside. Ukugcina isikhathi eside, ama-specimens kufanele agcinwe ngaphansi -20 ℃. Igazi eliphelele kufanele ligcinwe ku-2-8℃ uma ukuhlolwa kuzokwenziwa phakathi kwezinsuku ezi-2 zokuqoqwa. Ungawaqandi amasampula egazi eliphelele.
4.Letha ama-specimens ekamelweni lokushisa ngaphambi kokuhlolwa. Izifanekiso eziqandisiwe kufanele zincibilikiswe ngokuphelele futhi zixutshwe kahle ngaphambi kokuhlolwa. Izibonelo akufanele zifrizwe futhi zincibilikiswe ngokuphindaphindiwe.
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.Beka idivayisi yokuhlola endaweni ehlanzekile neleveli.
2.Ngokuhlolwa kwe-IgG/IgM :Bamba i-dropper ngokuqondile bese udlulisela iconsi elingu-1 lesifanekiso (cishe u-10μl) esibonelweni somthombo(S) wedivayisi yokuhlola, bese wengeza amaconsi angu-2 ebhafa (cishe u-70μl) bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
3.Okwe-NS1Test:
Okwesampula se-serum noma se-plasma: Bamba i-dropper ngokuqondile bese udlulisela amaconsi angu-8~10 e-serum noma i-plasma (cishe u-100μl) esibonelweni somthombo(S) wensiza yokuhlola, bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
Ngezifanekiso zegazi eliphelele: Bamba i-dropper ngokuqondile bese udlulisela amaconsi angu-3 egazi 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.
4.Linda ukuthi kuvele ulayini onemibala. Funda imiphumela ngemizuzu eyi-15. Ungahumushi umphumela ngemuva kwemizuzu engama-20.
Amanothi:
Ukusebenzisa inani elanele lesifanekiso kubalulekile ukuze uthole umphumela wokuhlola ovumelekile. Uma ukufuduka (ukumanziswa kolwelwesi) kungabonwa efasiteleni lokuhlola ngemva komzuzu owodwa, engeza ithonsi elilodwa lebhafa noma isifanekiso esibonelweni kahle.
Iphrofayela Yenkampani
Thina, i-Hangzhou Testsea Biotechnology CO., Ltd, singabakhiqizi abaqeqeshiwe abakhethekile ocwaningweni, ekuthuthukisweni nasekukhiqizeni amakhithi okuhlola ukuxilonga kwezokwelapha, ama-reagents nezinto zokuqala. sithengisa uhla olubanzi lwekhithi yokuhlola esheshayo yokuxilongwa komtholampilo, komndeni kanye nelebhu okuhlanganisa izinsiza zokuhlola inzalo, izinto zokuhlola izidakamizwa zokuhlukunyezwa, izinto zokuhlola izifo ezithathelwanayo, izinto zokuhlola umaka wesimila, okokuhlola ukuphepha kokudla, indawo yethu i-GMP, i-ISO CE eqinisekisiwe. . Sinefekthri yesitayela sengadi enendawo engaphezu kwamamitha-skwele ayi-1000, sinamandla acebile kwezobuchwepheshe, imishini ethuthukisiwe kanye nesistimu yokuphatha yesimanje, sesivele sigcinile ubudlelwano obuthembekile bebhizinisi namakhasimende ekhaya naphesheya. Njengomphakeli oholayo wokuhlolwa kokuxilonga okusheshayo kwe-in vitro, sihlinzeka ngesevisi ye-OEM ODM, sinamakhasimende eNyakatho naseNingizimu Melika, eYurophu, e-Oceania, empumalanga emaphakathi, eNingizimu-mpumalanga ye-Asia kanye nase-Afrika. Sithemba ngobuqotho ukuthuthukisa nokusungula ubudlelwano bebhizinisi obuhlukahlukene nabangane ngokusekelwe ezimisweni zokulingana nezinzuzo ezifanayo..
Okunye ukuhlolwa kwezifo ezithathelwanayo esikunikezayo
| Ikhithi Yokuhlola Esheshayo Yezifo Ezithathelwanayo |
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| Igama lomkhiqizo | Ikhathalogi No. | Isifanekiso | Ifomethi | Ukucaciswa | Isitifiketi | |
| I-Influenza Ag A Test | 101004 | I-Nasopharyngeal Swab | Ikhasethi | 25T | CE ISO | |
| Ukuhlolwa komkhuhlane we-Ag B | 101005 | I-Nasopharyngeal Swab | Ikhasethi | 25T | CE ISO | |
| I-HCV Hepatitis C Virus Ab Test | 101006 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-HIV 1/2 | 101007 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| HIV 1/2 Tri-line Test | 101008 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-HIV 1/2/O Amasosha omzimba | 101009 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| Ukuhlolwa kweDengue IgG/IgM | 101010 | I-WB/S/P | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Dengue NS1 Antigen | 101011 | I-WB/S/P | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Dengue IgG/IgM/NS1 Antigen | 101012 | I-WB/S/P | I-Dipcard | 40T | CE ISO | |
| Ukuhlolwa kwe-H.Pylori Ab | 101013 | I-WB/S/P | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-H.Pylori Ag | 101014 | Indle | Ikhasethi | 25T | CE ISO | |
| I-Syphilis (Anti-treponemia Pallidum) Ukuhlolwa | 101015 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kweTyphoid IgG/IgM | 101016 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Toxo IgG/IgM | 101017 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| Ukuhlolwa Kwesifo Sofuba | 101018 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| I-HBsAg Hepatitis B surface Antigen Test | 101019 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| I-HBsAb Hepatitis B Surface Antibody Test | 101020 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| Igciwane le-HBsAg Hepatitis B kanye ne-Antigen Test | 101021 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| I-HBsAg Igciwane le-Hepatitis B ne-Antibody Test | 101022 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| I-HBsAg I-Hepatitis B virus core Test | 101023 | I-WB/S/P | Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-Rotavirus | 101024 | Indle | Ikhasethi | 25T | CE ISO | |
| Ukuhlolwa kwe-Adenovirus | 101025 | Indle | Ikhasethi | 25T | CE ISO | |
| Ukuhlolwa kwe-Norovirus Antigen | 101026 | Indle | Ikhasethi | 25T | CE ISO | |
| I-HAV Hepatitis A virus Test IgM | 101027 | I-WB/S/P | Ikhasethi | 40T | CE ISO | |
| I-HAV Hepatitis A virus Test IgG/IgM | 101028 | I-WB/S/P | Ikhasethi | 40T | CE ISO | |
| I-Malaria Ag pf/pv Ukuhlolwa kwe-Tri-line | 101029 | WB | Ikhasethi | 40T | CE ISO | |
| I-Malaria Ag pf/pan Tri-line Test | 101030 | WB | Ikhasethi | 40T | CE ISO | |
| I-Malaria Ag pv Test | 101031 | WB | Ikhasethi | 40T | CE ISO | |
| I-Malaria Ag pf Test | 101032 | WB | Ikhasethi | 40T | CE ISO | |
| Umalaleveva Ag pan Test | 101033 | WB | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Leishmania IgG/IgM | 101034 | ISerum/Plasma | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Leptospira IgG/IgM | 101035 | ISerum/Plasma | Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Brucellosis(Brucella)IgG/IgM | 101036 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| Chikungunya IgM Test | 101037 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Chlamydia trachomatis Ag | 101038 | I-Endocervical Swab/Urethral swab | Umdweshu/Ikhasethi | 25T | ISO | |
| Ukuhlolwa kwe-Neisseria Gonorrhoeae Ag | 101039 | I-Endocervical Swab/Urethral swab | Umdweshu/Ikhasethi | 25T | CE ISO | |
| I-Chlamydia Pneumoniae Ab IgG/IgM Test | 101040 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| I-Chlamydia Pneumoniae Ab IgM Test | 101041 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| I-Mycoplasma Pneumoniae Ab IgG/IgM Test | 101042 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| I-Mycoplasma Pneumoniae Ab IgM Test | 101043 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | CE ISO | |
| Ukuhlolwa kwe-Rubella virus antibody IgG/IgM | 101044 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-Cytomegalovirus antibody IgG/IgM | 101045 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| I-Herpes simplex virus Ⅰ ukuhlolwa kwe-antibody IgG/IgM | 101046 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| I-Herpes simplex virus ⅠI antibody IgG/IgM test | 101047 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-Zika virus antibody IgG/IgM | 101048 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| Ukuhlolwa kwe-Hepatitis E virus antibody IgM | 101049 | I-WB/S/P | Umdweshu/Ikhasethi | 40T | ISO | |
| Ukuhlolwa komkhuhlane we-Ag A+B | 101050 | I-Nasopharyngeal Swab | Ikhasethi | 25T | CE ISO | |
| I-HCV/HIV/SYP Multi Combo Test | 101051 | I-WB/S/P | I-Dipcard | 40T | ISO | |
| I-MCT HBsAg/HCV/HIV Multi Combo Test | 101052 | I-WB/S/P | I-Dipcard | 40T | ISO | |
| I-HBsAg/HCV/HIV/SYP Multi Combo Test | 101053 | I-WB/S/P | I-Dipcard | 40T | ISO | |
| Ukuhlolwa kwe-Monkey Pox Antigen | 101054 | i-oropharyngeal swabs | Ikhasethi | 25T | CE ISO | |
| I-Rotavirus/Adenovirus Antigen Combo Test | 101055 | Indle | Ikhasethi | 25T | CE ISO | |
