I-SARS-CoV-2

  • Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    Inoveli Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    Inoveli coronavirus yintsholongwane ye-RNA, equlathe iiproteni kunye neecicic acid. Intsholongwane ingena kumzimba womntu (umntu), ingena kwiiseli kwindawo ebophayo ehambelana ne-receptor ACE2, kwaye iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphinde iphendule kwiintsholongwane zangaphandle kwaye ivelise izilwa-buhlungu ezithile. Ke ngoko, i-vial nucleic acid kunye neeantigen, kunye neentsholongwane ezithile ngokuchasene nenoveli coronavirus inokuthiyori ingasetyenziswa njengezinto ezithile zebhayomarker zokufumanisa inoveli coronavirus. Ukufumanisa i-nucleic acid, itekhnoloji ye-RT-PCR yeyona isetyenziswa kakhulu.

    Inoveli Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit yenzelwe ukuba isetyenziselwe ukufezekisa ubungakanani be-SARS_CoV-2 ye-virus ye-RNA ekhutshwe kwi-nasopharyngeal swabs, oropharyngeal swabs, isikhohlela kunye ne-BALF kwizigulana ezidibene ne-FDA / CE Inkqubo yokukhupha i-IVD kunye namaqonga e-PCR akhethiweyo adweliswe apha ngasentla.

    Le khithi yenzelwe ukuba isetyenziswe ngabasebenzi abaqeqeshiweyo elebhu

  • SARS-CoV-2 IgM/IgG Antibody Rapid Test

    I-SARS-CoV-2 IgM / IgG yovavanyo olukhawulezileyo lwe-Antibody

    IStrongStep®  I-SARS-CoV-2 IgM / IgG ye-Antibody Rapid Test kit isetyenziselwa ukubonwa kwe-vitro esemgangathweni kunye nokuchongwa kwesifo se-SARS-CoV-2 antibody coronavirus COVID-19 kwiserum / iplasma / iisampulu zegazi (kubandakanya igazi le-venous kunye negazi lomnwe). yezigulana ezikrokrelwayo ukuxilongwa kosulelo kunokusetyenziselwa ukufumanisa ukuba umntu uneempawu okanye umntu ongenasifo osulelayo kunye novavanyo lweemolekyuli okanye ulwazi lweklinikhi.

    Uvavanyo lilinganiselwe e-US ukusasazwa kwiilebhu eziqinisekiswe yi-CLIA ukwenza uvavanyo oluntsonkothileyo oluphezulu.

    Olu vavanyo aluzange luhlolwe yi-FDA.

    Iziphumo ezingalunganga aziluthinteli usulelo lwe-SARS-CoV-2.

    Iziphumo zovavanyo lwe-antibody akufuneki zisetyenziselwe ukuxilonga okanye ukukhuphela ngaphandle usulelo lwe-SARS-CoV-2.

    Iziphumo ezincumisayo zinokuba ngenxa yosulelo oludlulileyo okanye olukhoyo ngezifo ezingezizo ze-SARS-CoV-2 coronavirus, ezinje nge-coronavirus HKU1, NL63, OC43, okanye 229E.

  • SARS-CoV-2 Antigen Rapid Test

    Uvavanyo lweSARS-CoV-2 lwe-Antigen ekhawulezayo

    Isixhobo seDual Biosafety System seSARS-CoV-2 Antigen Test sisetyenziselwa ukufumanisa umgangatho wenoveli coronavirus (SARS-CoV-2) nucleocapsid (N) antigen kwi-Sroat / Nasopharyngeal swab sampuli kwi-vitro. Ikhithi kufuneka isetyenziswe kuphela njengesalathi esongezelelweyo okanye isetyenziswe ngokudibeneyo kunye nokufunyanwa kwe-acid ye-acid ekuchongeni imeko ye-COVID-19 ekrokrelwayo. Ayinakusetyenziswa njengesiseko sodwa ekuchongeni nasekugxothweni kwabaguli be-pneumonitis abasuleleke yinoveli coronavirus, kwaye ayikulungelanga ukuvavanywa kwabemi ngokubanzi. Iikiti zilungele ukusetyenziswa ekuhlolweni okukhulu kumazwe nakwimimandla apho inoveli yokuqhambuka kwenoveli isasazeka ngokukhawuleza, kunye nokubonelela ngoxilongo kunye nokuqinisekisa usulelo lwe-COVID-19.

    OKUBALULEKILEYO: LE MVELISO YENZELWE UKUSETYENZISWA NGOKUGQIBELA, HAYI UKUZIVIVINYA OKANYE UKUVAVANYA EKHAYA!

  • Dual Biosafety System Device for SARS-CoV-2 Antigen Rapid Test

    Isixhobo seDia Biosafety System seSARS-CoV-2 sovavanyo olukhawulezayo lweAntgen

    Isixhobo seDual Biosafety System seSARS-CoV-2 Antigen Test sisetyenziselwa ukufumanisa umgangatho wenoveli coronavirus (SARS-CoV-2) nucleocapsid (N) antigen kwi-Sroat / Nasopharyngeal swab sampuli kwi-vitro. Ikhithi kufuneka isetyenziswe kuphela njengesalathi esongezelelweyo okanye isetyenziswe ngokudibeneyo kunye nokufunyanwa kwe-acid ye-acid ekuchongeni imeko ye-COVID-19 ekrokrelwayo. Ayinakusetyenziswa njengesiseko sodwa ekuchongeni nasekugxothweni kwabaguli be-pneumonitis abasuleleke yinoveli coronavirus, kwaye ayikulungelanga ukuvavanywa kwabemi ngokubanzi. Iikiti zilungele ukusetyenziswa ekuhlolweni okukhulu kumazwe nakwimimandla apho inoveli yokuqhambuka kwenoveli isasazeka ngokukhawuleza, kunye nokubonelela ngoxilongo kunye nokuqinisekisa usulelo lwe-COVID-19. Ukuvavanywa kuthintelwe kwiilebhu eziqinisekisiweyo phantsi kwemigaqo yesizwe okanye yabasemagunyeni bendawo.

  • System Device for SARS-CoV-2 & Influenza A/B Combo Antigen Rapid Test

    Isixhobo seNkqubo ye-SARS-CoV-2 kunye ne-Influenza A / B Combo Antigen Rapid Test

    Isixhobo seNkqubo eStrongStep ® seSARS-CoV-2 kunye noMkhuhlane A / B weCombo Antigen Rapid Test usebenzisa uvavanyo lwe-chromatographic lateral test. Mithathu imicu kwesi sixhobo ifumanisa i-SARS-CoV-2, uhlobo lomkhuhlane u-A kunye nohlobo lwe-influenza ngokwahlukeneyo, iLatex conjugated antibody (Latex-Ab) engqinelana ne-SARS-CoV-2 / Flu A / Flu B yomile isiphelo senwebu nganye yenwebu ye-nitrocellulose. Ii-antibodies ze-SARS-CoV-2 / Flu A / Flu B ziyibhondi kuMmandla woVavanyo (T) kunye neBiotin-BSA zizibophelelo kuMmandla woLawulo (C) kumtya ngamnye. Xa isampulu yongezwa, ifuduka ngokusasazeka kwe-capillary iphinde ifake i-latex conjugate. Ukuba ikhona kwisampulu, ii-antigen ze-SARS-CoV-2 / Flu A / Flu B ziya kubopha kunye neentsholongwane ezincinci