Testsea Disease Test Typhoid IgG/IgM Test
Iinkcukacha eziKhawulezayo
Igama lebrand: | Testsea | Igama lemveliso: | Uvavanyo lweTyphoid IgG/IgM |
Indawo yemvelaphi: | Zhejiang, China | Uhlobo: | Izixhobo zokuHlalutya kwePathological |
Isatifikethi: | CE/ISO9001/ISO13485 | Ukuhlelwa kwesixhobo | Udidi III |
Ukuchaneka: | 99.6% | Umzekelo: | Igazi Elipheleleyo/iSerum/Plasma |
Ubume: | Ikhasethi | Inkcazo: | 3.00mm/4.00mm |
MOQ: | 1000 iiPC | Beka ubomi kwishelufa: | iminyaka eyi-2 |
OEM & ODM | inkxaso | Inkcazo: | 40pcs / ibhokisi |
Supply Ability:
5000000 Iqhekeza/Amaqhekeza ngenyanga
Ukupakishwa kunye nokuhanjiswa:
Iinkcukacha zokuPakisha
40pcs / ibhokisi
2000PCS/CTN,66*36*56.5cm,18.5KG
Ixesha lokukhokhela:
Ubuninzi (amaqhekeza) | 1 - 1000 | 1001 - 10000 | >10000 |
Ixesha lokuhamba (iintsuku) | 7 | 30 | Kuza kuthethathethwana |
Ukusetyenziswa okucetywayo
Uvavanyo olukhawulezayo lweTyphoid IgG/IgM (TYP tast cassette) yi-lateral flow immunoassay yokufumanisa ngaxeshanye kunye nokwahlukana kwe-anti-Salmonella typhi (S. typhi) IgG kunye ne-IgM kwi-serum yabantu, i-plasma.Yenzelwe ukuba isetyenziswe njengovavanyo lokuhlola kwaye njengoncedo ekuxilongeni usulelo nge-S. typhi.Nawuphi na umzekelo osebenzayo kunye noVavanyo oluKhawulezayo lweTyphoid IgG/IgM kufuneka luqinisekiswe ngenye indlela (iindlela zovavanyo).
Isishwankathelo
Umkhuhlane wetyphoid ubangelwa yi-S. typhi, intsholongwane ye-Gram-negative.Ehlabathini lonke kuqikelelwa ukuba zizigidi ezili-17 zezehlo kunye ne-600,000 yokufa okunxulumene noko kwenzeka ngonyaka1.Izigulana ezosulelwe yi-HIV zisengozini eyongezelelekileyo yosulelo lwezonyango nge-S. typhi2.Ubungqina bosulelo lwe-H. pylori bukwabonisa ukonyuka komngcipheko wokufumana i-typhoid fever.I-1-5% yezigulane ziba ngumthwali ongapheliyo ogcina i-S. typhi kwi-gallbladder.
Ukuxilongwa kwekliniki ye-typhoid fever kuxhomekeke ekubekweni yedwa kwe-S. typhi egazini, umongo okanye isilonda esithile se-anatomic.Kwizibonelelo ezingenakukwazi ukwenza le nkqubo enzima kunye nexesha elide, uvavanyo lweFilix-Widal lusetyenziselwa ukuququzelela ukuxilongwa.Nangona kunjalo, imida emininzi ikhokelela kubunzima ekutolikeni kovavanyo lwe-Widal3,4.
Ngokwahlukileyo koko, iTyphoid IgG/IgM Rapid Test luvavanyo olulula nolukhawulezayo lwaselabhoratri.Uvavanyo ngaxeshanye lufumanisa kwaye lwahlula-hlula i-IgG kunye ne-IgM antibodies kwi-S. typhi ethile ye-antigen5 t kwi-specimen yegazi lonke ngaloo ndlela inceda ekumiseleni ukubonakaliswa kwangoku okanye kwangaphambili kwi-S. typhi.
Inkqubo yoVavanyo
1. Uvavanyo lweOne Step lunokwenziwa lusetyenziswe kwilindle.
2. Qokelela umyinge owaneleyo welindle (1-2 ml okanye 1-2 g) kwindawo ecocekileyo, eyomileyo yokuqokelela isampuli ukuze ufumane ii-antigens eziphezulu (ukuba zikhona).Iziphumo ezingcono kakhulu ziya kufumaneka ukuba iimvavanyo zenziwe kwiiyure ze-6 emva kokuqokelela.
3.Isampuli eqokelelweyo ingagcinwa iintsuku ezi-3 kwi-2-8℃ ukuba ayivavanywanga kwiiyure ezi-6.Ukugcina ixesha elide, iisampuli kufuneka zigcinwe ngaphantsi -20 ℃.
4.Khumbula i-cap ye-tube yokuqokelela i-specimen, emva koko uhlabe ngokungenamkhethe i-specimen collection applicator kwi-fecal specimen ubuncinane kwiindawo ezi-3 ezahlukeneyo ukuqokelela malunga ne-50 mg ye-feces (elingana ne-1/4 ye-pea).Musa ukukhupha i-fecal ye-membrane) ayijongwa kwifestile yovavanyo emva komzuzu omnye, yongeza enye ithontsi yesampulu kwi-specimen kakuhle.
Okuhle: kuvela imigca emibini.Umgca omnye kufuneka uhlale uvela kumgca wolawulo (C), kwaye omnye umgca ocacileyo onemibala kufuneka uvele kwindawo yovavanyo.
Okubi: Umgca omnye onemibala ubonakala kummandla wolawulo (C) .Akukho mgca wombala obonakalayo ovela kummandla wovavanyo.
Ayisebenzi: Umgca wolawulo awubonakali.Umthamo ongonelanga wesampulu okanye ubuchule benkqubo obungachanekanga zezona zizathu zinokwenzeka zokungaphumeleli komgca wolawulo.
★ Hlaziya inkqubo kwaye uphinda uvavanyo ngesixhobo esitsha sovavanyo.Ukuba ingxaki iyaqhubeka, yeka ukusebenzisa ikiti yovavanyo ngoko nangoko kwaye uqhagamshelane nomsasazi wakho wendawo.
Uluhlu lweeMveliso
Igama lemveliso | Umzekelo | Ifomathi | Isatifikethi |
Umkhuhlane Ag A Uvavanyo | Ngempumlo / Nasopharyngeal Swab | Ikhasethi | CE ISO |
Uvavanyo lwe-Influenza Ag B | Ngempumlo / Nasopharyngeal Swab | Ikhasethi | CE ISO |
HCV Hepatitis C Virus Ab Uvavanyo | WB/S/P | Ikhasethi | ISO |
HIV 1+2 Test | WB/S/P | Ikhasethi | ISO |
HIV 1/2 Tri-line Test | WB/S/P | Ikhasethi | ISO |
HIV 1/2/O Antibody Test | WB/S/P | Ikhasethi | ISO |
Uvavanyo lweDengue IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweDengue NS1 Antigen | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweDengue IgG/IgM/NS1 Antigen | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lwe-H.Pylori Ab | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lwe-H.Pylori Ag | Ilindle | Ikhasethi | CE ISO |
Uvavanyo lweSyphilis (Anti-treponemia Pallidum). | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweTyphoid IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lwe-Toxo IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweSifo sePhepha | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo olukhawulezayo lwe-HBsAg | WB/S/P | Ikhasethi | ISO |
Uvavanyo oluKhawulezayo lwe-HBsAb | WB/S/P | Ikhasethi | ISO |
HBeAg Rapid Test | WB/S/P | Ikhasethi | ISO |
Uvavanyo oluKhawulezayo lweHBeAb | WB/S/P | Ikhasethi | ISO |
Uvavanyo oluKhawulezayo lwe-HBcAb | WB/S/P | Ikhasethi | ISO |
Uvavanyo lweRotavirus | Ilindle | Ikhasethi | CE ISO |
Uvavanyo lweAdenovirus | Ilindle | Ikhasethi | CE ISO |
Uvavanyo lwe-Norovirus Antigen | Ilindle | Ikhasethi | ISO |
Uvavanyo lwe-IgM ye-HAV Hepatitis A | WB/S/P | Ikhasethi | ISO |
Uvavanyo lwe-HAV Hepatitis A lwe-IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
IMalaria Ag pf/pv Uvavanyo lomgca wesithathu | WB | Ikhasethi | CE ISO |
Malaria Ag pf/pan Uvavanyo lomgca wesithathu | WB | Ikhasethi | ISO |
IMalariya Ab pf/pv Uvavanyo lomgca wesithathu | WB | Ikhasethi | CE ISO |
Uvavanyo lweMalariya Ag pv | WB | Ikhasethi | CE ISO |
Uvavanyo lweMalariya Ag pf | WB | Ikhasethi | CE ISO |
Malaria Ag pan Test | WB | Ikhasethi | CE ISO |
Uvavanyo lweLeishmania IgG/IgM | ISerum/Plasma | Ikhasethi | CE ISO |
Uvavanyo lweLeptospira IgG/IgM | ISerum/Plasma | Ikhasethi | CE ISO |
Uvavanyo lweBrucellosis(Brucella)IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Chikungunya IgM Test | WB/S/P | Ikhasethi | CE ISO |
Chlamydia trachomatis Ag Test | I-Endocervical Swab / Urethral swab | Ikhasethi | ISO |
Uvavanyo lweNeisseria Gonorrhoeae Ag | I-Endocervical Swab / Urethral swab | Ikhasethi | CE ISO |
Uvavanyo lweChlamydia Pneumoniae Ab IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweChlamydia Pneumoniae Ab IgM | WB/S/P | Ikhasethi | ISO |
Uvavanyo lweMycoplasma Pneumoniae Ab IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweMycoplasma Pneumoniae Ab IgM | WB/S/P | Ikhasethi | CE ISO |
Intsholongwane yeRubella ye-Ab IgG/IgM Test | WB/S/P | Ikhasethi | CE ISO |
Cytomegalo virus Antibody IgG/IgM Test | WB/S/P | Ikhasethi | CE ISO |
Herpes simplex virus Ⅰ antibody IgG/IgM test | WB/S/P | Ikhasethi | CE ISO |
Herpes simplex virus Ⅱ antibody IgG/IgM test | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lweZika virus antibody IgG/IgM | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lwe-IgM yentsholongwane ye-Hepatitis E | WB/S/P | Ikhasethi | CE ISO |
Uvavanyo lwe-Influenza Ag A + B | Ngempumlo / Nasopharyngeal Swab | Ikhasethi | CE ISO |
HCV/HIV/SYP Multi Combo Test | WB/S/P | Ikhasethi | ISO |
Uvavanyo lwe-MCT HBsAg/HCV/HIV Multi Combo Test | WB/S/P | Ikhasethi | ISO |
Uvavanyo lwe-HBsAg/HCV/HIV/SYP Multi Combo | WB/S/P | Ikhasethi | ISO |
Monkey Pox Antigen Test Cassette | I-Oropharyngeal swab | Ikhasethi | CE ISO |
Iimveliso ezinxulumeneyo
Ulwazi Lomboniso
Isatifikethi sembeko
Iprofayile yekhampani
Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokukhawuleza yobuchwephesha bebhayoloji ekhethekileyo ekuphandeni, ekuphuhliseni, ekuveliseni nasekusasazeni iikhithi zovavanyo lwe-in-vitro diagnostic (IVD) kunye nezixhobo zonyango.
Indawo yethu yi-GMP, ISO9001, kunye ne-ISO13458 eqinisekisiweyo kwaye sinemvume ye-CE FDA.Ngoku sijonge phambili ekusebenzisaneni neenkampani zaphesheya kwezilwandle ngophuhliso olufanayo.
Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, uvavanyo lokusetyenziswa kakubi kweziyobisi, uvavanyo lwentliziyo, uvavanyo lokumakisha ithumba, uvavanyo lokutya kunye nokhuseleko kunye novavanyo lwezifo zezilwanyana, ukongezelela, uphawu lwethu lwe-TESTSEALABS luye lwaziwa kakhulu kwiimarike zasekhaya naphesheya.Umgangatho ogqwesileyo kunye namaxabiso ancomekayo asenza sikwazi ukuthatha ngaphezulu kwe-50% yezabelo zasekhaya.
OUKUPAKISHA & UKUTHUMELA
FAQ
Sizinze eZhejiang, eChina, siqale ngo-2015, sithengisela uMzantsi-mpuma Asia (15.00%), iMarike yasekhaya (15.00%), eMzantsi, eMelika (10.00%), eAfrika (10.00%), eMntla Melika (5.00%), eMpuma
IYurophu(5.00%), i-Oceania(5.00%), uMbindi Mpuma(5.00%),eMpuma Asia(5.00%),iNtshona Yurophu(5.00%),uMbindi Merika(5.00%), uMntla Yurophu(5.00%),uMzantsi Yurophu( 5.00%),South Asia(5.00%).Kukho abantu abamalunga nama-51-100 eofisini yethu.
Ngalo lonke ixesha isampuli yangaphambi kokuveliswa phambi kokuveliswa kobuninzi;
Ukuhlolwa kokugqibela rhoqo ngaphambi kokuthunyelwa;
Uvavanyo oluKhawulezayo lwezilwanyana, iiKhithi zoVavanyo lokuchuma, iiKhithi zoVavanyo lweSiyobisi, iiKhithi zoVavanyo lweSifo esosulelayo, uVavanyo lwaMakishi eTumor, uvavanyo loKhuseleko lokutya
Amandla atyebileyo kwitekhnoloji, izixhobo eziphambili, inkqubo yolawulo lwangoku, uluhlu olubanzi lweekhithi zovavanyo olukhawulezayo lweklinikhi, usapho kunye nokuxilongwa kwelebhu, ISO, CE FSC eqinisekisiweyo.
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