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Uvavanyo lwabantu

  • Ikhithi yoVavanyo lweChlamydia Rapid Kit elula yovavanyo

    Ikhithi yoVavanyo lweChlamydia Rapid Kit elula yovavanyo

    Uvakalelo Isixhobo soVavanyo oluKhawulezayo lweChlamydia siye savavanywa ngeeseli ezosulelekileyo zeChlamydia kunye nesampulu ezifunyenwe kwizigulana zeekliniki ze-STD.I-Chlamydia Rapid Test Device inokubona i-107 org/ml.Ukuchaneka IsiXhobo soVavanyo oluKhawulezayo lwe-Chlamydia sisebenzisa i-antibody ekhetheke kakhulu kwi-Chlamydia antigen kwisampulu.Iziphumo zibonisa i-Chlamydia Rapid Test Device ine-speciality ephezulu ngokumalunga nolunye uVavanyo lwe-Female Cervical Swab Specimens: Indlela yolunye uvavanyo lulonke ...
  • Uvavanyo olukhawulezileyo lweziyobisi lwe-Urine MET TEST KIT, uvavanyo lweziyobisi ezininzi, ikhadi leDip, iPhaneli

    Uvavanyo olukhawulezileyo lweziyobisi lwe-Urine MET TEST KIT, uvavanyo lweziyobisi ezininzi, ikhadi leDip, iPhaneli

    Ukuchaneka Uthelekiso olusecaleni lwenziwe kusetyenziswa iMET One Step Methamphetamine Test kunye novavanyo olukhawulezayo lweMET olufumanekayo kwezorhwebo.Uvavanyo lwenziwa kwiisampuli zeklinikhi ezingama-234.Ishumi leepesenti leesampulu eziqeshiweyo mhlawumbi kwi-25% okanye +25% kwinqanaba le-concentration ye-cut-off ye-1,000 ng/mL Methamphetamine.Iziphumo ezilungileyo ezicingelwayo ziqinisekiswe yiGC/MS.Ezi ziphumo zilandelayo zidweliswe: Indlela Olunye uvavanyo lwe-MET oluKhawulezayo lulonke lweZiphumo ziMET kwiSixhobo esinye soVavanyo lweNyathelo elinye...
  • Umgangatho ophezulu we-KET woVavanyo lweChiza leDip Card, iPhaneli

    Umgangatho ophezulu we-KET woVavanyo lweChiza leDip Card, iPhaneli

    Ukuchaneka Ukuthelekisa kuqhutywe kusetyenziswa i-KET One Step Ketamine Test kunye ne-GC / MS kwi-1,000 ng / mL cut-off.Ezi ziphumo zilandelayo zidweliswe: Indlela ye-GC/MS Iyonke yeZiphumo ze-KET inyathelo elinye Iziphumo zovavanyo zi-Positive Negative 10 8 18 Negative 0 205 205 Zizonke iziphumo 10 213 223 % Isivumelwano 100% 96.2% 96.4% Analytical-free spitivity kunye neKetamine kwezi zigxina zilandelayo: 0 ng / mL, 500ng / mL, 750 ...
  • I-Instant Urine Test Kit K2 – CE ivunyiwe

    I-Instant Urine Test Kit K2 – CE ivunyiwe

    A. Uvakalelo Inyathelo elinye leCannabis yeSynthetic (K2) Uvavanyo lusete ukunqunyulwa kwesikrini kwimizekelo emihle kwi-25 ng/mL ye-JWH-018 Pentanoic Acid kunye ne-JWH-073 Butanoic Acid njengezikali.Isixhobo sovavanyo singqinwe ukuba sichonge ngaphezulu kwenqanaba lokunqunyulwa kweziyobisi ekujoliswe kuzo kumchamo ngemizuzu emi-5.B.Ukucaciswa kunye nokusebenza okunqamlezileyo Ukuvavanya ukuchaneka kovavanyo, isixhobo sokuvavanya sasetyenziselwa ukuvavanya i-Synthetic Cannabis (K2), i-metabolites yayo kunye nezinye izinto zeklasi ezifanayo ezinokuthi...
  • UVavanyo oluKhawulezayo lwe-COC yeSixhobo soNyango esiPhakamileyo samachiza

    UVavanyo oluKhawulezayo lwe-COC yeSixhobo soNyango esiPhakamileyo samachiza

    A. Uvakalelo lweNyathelo elinye loVavanyo lweCocaine lusete ukunqunyulwa kwesikrini kwimizekelo emihle kwi-300 ng/mL ye-benzoylecgonine njenge-calibrator.Isixhobo sovavanyo sibonakaliswe ukuba sibona ngaphezulu kwe-300 ng/mL yeCocaine kumchamo kwimizuzu emi-5.B. Ukuchaneka kunye ne-cross reactivity Ukuvavanya ukuchaneka kovavanyo, isixhobo sokuvavanya sisetyenziselwa ukuvavanya i-Cocaine, i-metabolites yayo kunye namanye amacandelo eklasi efanayo enokuthi ibe khona kumchamo, Zonke izinto zongezwa kwiziyobisi. umntu oqhelekileyo...
  • Ukuchaneka okuphezulu Ikiti yoVavanyo lweSifo esosulelayo seTyphoid

    Ukuchaneka okuphezulu Ikiti yoVavanyo lweSifo esosulelayo seTyphoid

    Ukusebenza kweKlinikhi kuVavanyo lwe-IgM Iyonke iisampulu ezingama-334 ezivela kwizifundo ezisesichengeni ziye zavavanywa luVavanyo oluKhawulezayo lweTyphoid Antibody kunye ne-S. typhi IgM EIA yorhwebo.Ukuthelekisa zonke izifundo kuboniswe kolu luhlu lulandelayo.Indlela ye-IgM EIA Iyonke Iziphumo zovavanyo oluKhawulezayo lweTyphoid Antibody Positive Negative 31 2 33 Negative 3 298 301 Zizonke iziphumo 34 300 334 Uvakalelo olunxulumeneyo: 91.2% (76.3% - 98.1%)* Ubungakanani be-99...
  • Uvavanyo lweSixhobo soNyango se-CE esiphawulwe kwikhithi yoVavanyo lweSyphilis

    Uvavanyo lweSixhobo soNyango se-CE esiphawulwe kwikhithi yoVavanyo lweSyphilis

    OKUHLE:* Kuvela imigca emibini.Umgca omnye onemibala kufuneka ube kwindawo yokulawula umgca (C) kwaye omnye umgca wembala obonakalayo kufuneka ube kwindawo yovavanyo (T).*QAPHELA: Ubunzulu bombala kwingingqi yovavanyo (T) buya kwahluka ngokuxhomekeka kuxinzelelo lwe-TP antibodies ekhoyo kumzekelo.Ngoko ke, nawuphi na umthunzi wombala kwingingqi yovavanyo (T) kufuneka ithathwe njengelungileyo.I-NEGATIVE: Umgca omnye onemibala ubonakala kwindawo yokulawula umgca (C).Akukho mgca uvelayo kuluhlu lovavanyo...
  • I-CE evunyiweyo yehoseyile yeSixhobo sezoNyango Strep Ikhithi yoVavanyo

    I-CE evunyiweyo yehoseyile yeSixhobo sezoNyango Strep Ikhithi yoVavanyo

    Itheyibhile yokuchaneka: Strep A AntigenRapid Test vs. PCR Test Method Culture Iyonke Iziphumo Strep A Antigen Rapid Test Results Positive Negative 102 7 109 Negative 6 377 383 Total Iziphumo 108 384 492 Relative Sensitivity% (98.4%)% (98.4%). Ukuchaneka: 98.2% (96.3% -99.3%)* Ukuchaneka: 97.4% (95.5% -98.6%)* * 95% Amathuba okuzithemba OKUHLOSIWEYO I-Strep A Antigen Rapid Test yi- rapid chromatographic immunoassay yomgangatho...
  • Inyathelo elinye Ukuchaneka okuphezulu kweCE evunyiweyo kwekhithi yoVavanyo lweMalaria Pf/Pan

    Inyathelo elinye Ukuchaneka okuphezulu kweCE evunyiweyo kwekhithi yoVavanyo lweMalaria Pf/Pan

    Uvakalelo I-Malaria Pf/I-Pan Rapid Test Isixhobo (iGazi Elipheleleyo) ivavanyiwe ngemakroskopu ebhityileyo okanye engqindilili kwiisampulu zeklinikhi.Iziphumo zibonisa ukuba ubuntununtunu beMalaria Pf/Pan Rapid Test Device (Igazi Elipheleleyo) yi>99.9% xa kuthelekiswa nemicroscope.Kwi-Pan: Uvakalelo olunxulumeneyo: >99.9% (103/103) (96.5%~100.0%)* Kwi-Pf: Uvakalelo olunxulumeneyo: >99.9% (53/53) (93.3%~100.0%)* Ukuchaneka kweMalaria Pf/Pan IsiXhobo soVavanyo oluKhawulezayo (iGazi eliPheleleyo) lisebenzisa izilwa-buhlungu ezithe ngqo kwi-M...
  • Inyathelo elinye eliphezulu lokuchaneka kweMalaria Pf/Pv Test kit

    Inyathelo elinye eliphezulu lokuchaneka kweMalaria Pf/Pv Test kit

    Uvakalelo I-Malaria Pf/Pv Rapid Test Device (Igazi Elipheleleyo) ivavanyiwe ngemakroskopu kwiisampulu zeklinikhi.Iziphumo zibonisa ukuba ubuntununtunu beMalaria Pf/Pv Rapid Test Device (Igazi Elipheleleyo) yi>98% xa kuthelekiswa neziphumo ezifunyenwe ngemicroscope.Ukuchaneka I-Malaria Pf/Pv Rapid Test Device (Igazi Elipheleleyo) isebenzisa izilwa-buhlungu ezithe ngqo kwi-Malaria Pf-specific kunye ne-P.vivax LDH antigens kwigazi elipheleleyo.Iziphumo zibonisa ukuba ukuchaneka kwe ...
  • Ukusetyenziswa kwezonyango kwikiti yoVavanyo lweTyphoid, inyathelo elinye lovavanyo olukhawulezayo lwekhasethi

    Ukusetyenziswa kwezonyango kwikiti yoVavanyo lweTyphoid, inyathelo elinye lovavanyo olukhawulezayo lwekhasethi

    Uvakalelo lweKlinikhi, Ukuchaneka nokuchaneka Uvavanyo oluKhawulezayo loMkhuhlane A+B lwe-Antigen luvavanyiwe xa luthelekiswa ne-RT-PCR.I-539 ye-nasopharyngeal swabs kunye ne-oropharyngeal swabs zavandlakanywa kunye novavanyo olukhawulezayo lwe-Influenza A + B.Izinto eziManyeneyo eZinto zokuNxibelela kwiiNcinci zokuFafaza ngeempumlo 15% v/v I-Hemoglobin 10% v/v Mucin 0.5 % w/v Mupirocin 10 mg/mL Amathontsi eempumlo 15% v/v Ukuhlamba umlomo / iChloraseptic 1.5 mg/mL Levofloxacin 40 ug/mL2 mL...
  • CE ivunyiwe H. Pylori Ag Rapid Test kit, uvavanyo Cassette

    CE ivunyiwe H. Pylori Ag Rapid Test kit, uvavanyo Cassette

    IIMPAWU ZOKUSEBENZA Itheyibhile: H. Pylori Ag Uvavanyo oluKhawulezayo vs. Biopsy/Histology/RUT Relative Sensitivity: >95.0% (90.0%-97.9%)* INgcaciso eNxulumeneyo: >95.7% (92.3%-97.9%)* I-Agree iyonke > 5. % (92.8%-97.3%)* *95% iThuba lokuZithemba H. Pylori Ag Rapid Test + - Total Biopsy/ Histology/ RUT + 131 7 138 - 10 225 235 141 232 373 OKUHLOSIWE UKUSEBENZISA I-H. Rapidri Test A. I-Feces) luvavanyo olukhawulezayo lwe-chromatographic yokukhangela umgangatho wee-antigens ...