Ikhithi yokuHlola 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:Imizuzu eyi-10-15
  • 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 yoMfanekiso 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/i-plasma/iisampulu zegazi elipheleleyo njengoncedo ekuxilongeni intsholongwane 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 ye-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%)

    Lilonke izinga lokuzenzekela: 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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