Ikhithi yokuxilonga ye-Antibody ukuya kwiNtsholongwane kaGawulayo yoMntu i-HIV Colloidal Gold

inkcazelo emfutshane:

Ikhithi yokuxilonga ye-Antibody ukuya kuMntu
Intsholongwane ye-Immunodeficiency (i-Colloidal Gold)

 


  • Ixesha lovavanyo:10-15 imizuzu
  • Ixesha elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:1/25 uvavanyo / ibhokisi
  • Ubushushu bokugcina :2℃-30℃
  • Indlela yokusebenza:Igolide yeColloidal
  • Iodolo (MOQ):Iimvavanyo ezingama-500
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    Ikhithi yokuxilonga ye-Antibody ukuya kwiNtsholongwane yoKhuseleko loMntu (i-Colloidal Gold)

    Ulwazi lwemveliso

    Inombolo yoMzekelo HIV Ukupakisha Iimvavanyo ze-25 / ikiti, i-30kits / i-CTN
    Igama Ikhithi yokuxilonga ye-Antibody ukuya kwiNtsholongwane yoKhuseleko loMntu (i-Colloidal Gold) Ukuhlelwa kwesixhobo Udidi III
    Iimbonakalo Uvakalelo oluphezulu, ukusebenza ngokulula Isatifikethi CE/ ISO13485
    Ukuchaneka > 99% Beka ubomi kwishelufa Iminyaka emibini
    Indlela yokusebenza Igolide yeColloidal Inkonzo ye-OEM/ODM Iyafumaneka

     

    Inkqubo yovavanyo

    1 Thatha isixhobo sovavanyo kwisingxobo sefoyile ye-aluminiyam, usibeke phezu kwetafile ethe tyaba kwaye umakishe kakuhle isampulu.
    2 Kwiisampuli ze-serum kunye ne-plasma, thabatha amaconsi ama-2 kwaye uwafake kwi-spiked well;nangona kunjalo, ukuba isampuli yisampuli yegazi lonke, thatha amathontsi ama-2 kwaye uwafake kwi-spiked kakuhle kwaye kufuneka udibanise i-1 ye-drop ye-diluent yesampuli.
    3 Isiphumo kufuneka sifundwe kwimizuzu eyi-15-20.Iziphumo zovavanyo aziyi kusebenza emva kwemizuzu engama-20.

    Injongo yokuSebenzisa

    Le khithi ilungele ubhaqo kwi-in vitro qualitative virus human immunodeficiency virus HIV (1/2) amajoni omzimba kwi-serum yabantu/iplasma/iisampulu zegazi elipheleleyo njengoncedo ekuxilongweni kwentsholongwane kaGawulayo (1/2) ye-antibody.Le khithi ibonelela ngeziphumo zovavanyo lwe-HIV kuphela kwaye iziphumo ezifunyenweyo kufuneka zihlalutywe kunye nolunye ulwazi lwezonyango.Yenzelwe ukusetyenziswa ngabasebenzi bezonyango kuphela.

    HIV

    Isishwankathelo

    Ugawulayo, othetha ngeAcquired Immunodeficiency Syndrome, sisifo esosulelayo esinganyangekiyo nesibulalayo esibangelwa yiNtsholongwane kaGawulayo (i-HIV), esosulela ubukhulu becala ngokwabelana ngesondo kunye nokwabelana ngeesirinji, ngokunjalo nangosulelo olusuka kumama lusiya emntwaneni nolosulelo lwegazi. .I-HIV yi-retrovirus ehlasela kwaye ngokuthe ngcembe iwonakalisa amajoni omzimba womntu, ibangela ukuncipha kokusebenza kwamajoni omzimba kwaye yenze umzimba ube sesichengeni sosulelo kwaye ekugqibeleni ufe.Uvavanyo lwe-antibody lwe-HIV lubalulekile kuthintelo losulelo lwe-HIV kunye nonyango lwe-antibodies ye-HIV.

     

    Uphawu:

    • Uvakalelo oluphezulu

    • iziphumo zokufunda kwimizuzu eli-15

    • Ukusebenza ngokulula

    • Ixabiso elithe ngqo kwifektri

    • Awudingi umatshini owongezelelweyo wokufunda iziphumo

     

    Ikhithi ye-HIV rapiddiagnosis
    iziphumo zovavanyo

    Ukufundwa kweziphumo

    Uvavanyo lwe-reagent ye-WIZ BIOTECH luya kuthelekiswa ne-reagent yokulawula:

    Iziphumo zeWIZ Iziphumo zovavanyo lwereyinti yereferensi
    Okuhle Ibi Iyonke
    Okuhle 83 2 85
    Ibi 1 454 455
    Iyonke 84 456 540

    Izinga leziganeko ezilungileyo: 98.81% (95% CI 93.56% ~ 99.79%)

    Ireyithi yeziganeko ezimbi: 99.56% (95% CI98.42% ~ 99.88%)

    Ireyithi yeziganeko ezizenzekelayo: 99.44% (95% CI98.38% ~ 99.81%)

    Unokuthanda kwakhona:

    HCV

    IKhiti yoVavanyo oluKhawulezayo lweHCV Inyathelo elinye iHepatitis C Virus Antibody Rapid Test Kit

     

    Hp-Ag

    Ikhithi yokuxilonga yeAntigen ukuya kwiHelicobacter Pylori (HP-AG) NgeCE evunyiweyo

    VD

    Diagnostic Kit 25-(OH)VD TEST Kit Quantitative Kit POCT Reagent


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