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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 ... -
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
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
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
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
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
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
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 ... -
Umgangatho woBonelelo loMvelisi H. Pylori Ab Rapid Test kit
IIMPAWU ZOKUSEBENZA Itheyibhile: H. pylori Rapid Test vs. Biopsy/Histology/RUT Relative Sensitivity: >95.0% (90.0% -97.9%)* INkalo eNxulumeneyo: >95.7% (92.3%-97.9%)* Isivumelwano sisonke > 95%.4%. (92.8%-97.3%)* *95% iXesha lokuZithemba H.Pylori Rapid Test + - Total Biopsy/ Histology/ RUT + 131 7 138 - 10 225 235 141 232 373 UKUSETYENZISWA OKUHLOSIWEYO I-H.Pylori Test Blood Device (Wudho) /iSerum/ iPlasma) yinkqubo ekhawulezayo yokuxilonga i-chromatographic... -
Ikiti yovavanyo lwe-Medical Diagnostic Dengue NS1, uvavanyo olukhawulezayo
INKQUBO YOVAVANYO INyathelo 1: Yiza nomzekelo kunye nezixhobo zovavanyo kwiqondo lobushushu begumbi ukuba ifriji okanye ikhenkcezisiwe.Xuba isampuli kakuhle phambi kokuba uvavanyo xa lunyibilikisiwe.Inyathelo 2: Xa ulungele ukuvavanya, vula isingxobo kwinotshi kwaye ususe isixhobo.Beka isixhobo sovavanyo kwindawo ecocekileyo nesicaba.Inyathelo lesi-3: Qinisekisa ukuba uleyibhelishe isixhobo ngenombolo yesazisi yomzekelo.Inyathelo lesi-4: Kwisampulu yegazi elipheleleyo: Gcwalisa idropha ngesampulu emva koko wongeze amathontsi ama-2 (App.50µL) omzekelo kwisampulu yequla.Ukuqinisekisa ukuba kukho...
