Ikhithi yokuhlola ye-PSA Prostate Specific Antigen

Incazelo emfushane:

I-PSA Rapid Test iwukuhlola kwe-immunochromatographic ukuze kutholwe ikhwalithi ye-Prostate Specific Antigen (PSA) ku-serum yomuntu noma isampula se-plasma. Kuhloswe ukuthi kusetshenziswe njengokuhlolwa kokuhlola futhi njengosizo ekuhlonzweni komdlavuza wendlala yesinye.

Ukuzwela okuphezulu okunembile kanye nokucaciswa kokutholwa kwe-Prostate Specific Antigen (PSA) ku-serum yomuntu noma i-plasma.

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Imininingwane Yomkhiqizo

Omaka bomkhiqizo

Ithebula lepharamitha

Inombolo Yemodeli	I-TSIN101
Igama	I-PSA Prostate Specific Antigen Qualititive Test Kit
Izici	Ukuzwela okuphezulu, kulula, kulula futhi kunembile
Isifanekiso	I-WB/S/P
Ukucaciswa	3.0mm 4.0mm
Ukunemba	99.6%
Isitoreji	2'C-30'C
Ukuthumela ngomkhumbi	Ngolwandle/Ngomoya/TNT/Fedx/DHL
Ukuhlukaniswa kwezinsimbi	Ikilasi II
Isitifiketi	CE ISO FSC
Impilo yeshelufu	iminyaka emibili
Uhlobo	Izinsiza Zokuhlaziya I-Pathological

I-HIV 382

Isimiso se-FOB Rapid Test Device

I-PSA Rapid Test Device (Igazi Eliphelele) ithola ama-antigen athile e-prostate ngokutolika okubonakalayo kokuthuthukiswa kombala emgqeni wangaphakathi. Amasosha omzimba e-PSA awanyakazi endaweni yokuhlola yolwelwesi. Ngesikhathi sokuhlolwa, isifanekiso sibhekana namasosha omzimba e-PSA ahlanganiswe ezinhlayiyeni ezinemibala futhi ahlanganiswe ngaphambili kuphedi yesampula yokuhlolwa. Ingxube ibe isihamba nge-membrane ngesenzo se-capillary, futhi ixhumana nama-reagents kulwelwesi. Uma kune-PSA eyanele kusifanekiso, ibhande elinemibala lizokwakheka endaweni yokuhlola yolwelwesi. Ibhendi yokuhlola (T) ye-singal ebuthakathaka kunebhendi yereferensi (R) ibonisa ukuthi ileveli ye-PSA kusifanekiso iphakathi kuka-4-10 ng/mL. Isignali yebhendi yokuhlola (T) elingana noma esondelene nebhendi yereferensi (R) ibonisa ukuthi ileveli ye-PSA kusifanekiso icishe ibe ngu-10 ng/mL. Isignali yebhendi yokuhlola (T) enamandla kunebhendi yereferensi (R) ibonisa ukuthi ileveli ye-PSA kusifanekiso ingaphezu kuka-10 ng/mL. Ukubonakala kwebhande elinemibala endaweni yokulawula kusebenza njengokulawula kwenqubo, okubonisa ukuthi umthamo ofanele we-specimen wengeziwe futhi i-membrane wicking yenzekile.

I-PSA Rapid Test Device (Igazi Eliphelele/I-Serum/Plasma) iwukuhlolwa kwegazi okubonakalayo okusheshayo kokutholwa kokuqagela kwekhwalithi kwama-antigen athile e-prostate egazini lonke lomuntu, i-serum, noma izibonelo ze-plasma. Le kit ihloselwe ukusetshenziswa njengosizo ekuhlonzweni komdlavuza wendlala yesinye.

I-HIV 382

Inqubo Yokuhlola

Letha izivivinyo, ama-specimens, ibhafa kanye/noma izilawuli ekamelweni lokushisa ngaphambi kokusetshenziswa.

1. Khipha isivivinyo esikhwameni saso esivaliwe, bese usibeka endaweni ehlanzekile, esezingeni. Lebula idivayisi ngesihlonzi sesiguli noma sokulawula. Ukuze uthole imiphumela engcono kakhulu, ukuhlolwa kufanele kwenziwe lingakapheli ihora elilodwa.

2. Dlulisela amaconsi angu-1 e-serum/plasma esibonelweni somthombo (S) wedivayisi ngepayipi elilahlwayo elinikeziwe, bese wengeza ithonsi elingu-1 lebhafa, bese uqala isibali sikhathi.
OR
Dlulisela amaconsi angu-2 egazi eliphelele esibonelweni somthombo (S) wedivayisi ngepayipi elilahlwayo elinikeziwe, bese wengeza ithonsi elingu-1 lebhafa, bese uqala isibali sikhathi.
OR
Vumela amaconsi ama-2 alengayo wegazi eliphelele leminwe ukuthi awele phakathi nendawo yesifanekiso somthombo (S) wedivayisi yokuhlola, bese wengeza iconsi elingu-1 lebhafa, bese uqala isibali sikhathi.
Gwema ukubamba amabhamuza omoya esibonelweni kahle (S), futhi ungangezi noma yisiphi isisombululo endaweni yomphumela.
Njengoba ukuhlola kuqala ukusebenza, umbala uzohamba udlulele kulwelwesi.

3. Linda ukuthi amabhendi anombala avele. Umphumela kufanele ufundwe ngemizuzu eyi-10. Ungahumushi umphumela ngemuva kwemizuzu engama-20.

OKUQUKETHWE EKHITHI

I-PSA Rapid Test Device (Igazi Eliphelele) iwukuhlolwa kwegazi okubonakalayo okusheshayo kokutholwa kokuqagela kwekhwalithi kwama-antigen athile e-prostate egazini lonke lomuntu, i-serum, noma izibonelo ze-plasma. Le kit ihloselwe ukusetshenziswa njengosizo ekuhlonzweni komdlavuza wendlala yesinye.

I-HIV 382

UKUTOLIZWA KWEMIPHUMELA

Okuhle (+)

Amabhendi e-Rose-pink ayabonakala kokubili endaweni yokulawula kanye nesifunda sokuhlola. Ibonisa umphumela omuhle we-hemoglobin antigen.

Okubi (-)

Ibhendi ye-rose-pink ibonakala endaweni yokulawula. Alikho ibhande lombala elivelayo endaweni yokuhlola. Kubonisa ukuthi ukugcwala kwe-hemoglobin antigen kunguziro noma kungaphansi komkhawulo wokutholwa kokuhlolwa.

Akuvumelekile

Alikho nhlobo ibhande elibonakalayo, noma kukhona ibhendi ebonakalayo kuphela endaweni yokuhlola kodwa hhayi endaweni yokulawula. Phinda ngekhithi entsha yokuhlola. Uma ukuhlolwa kusahluleka, sicela uxhumane nomsabalalisi noma isitolo, lapho uthenge khona umkhiqizo, ngenombolo yelotho.

I-HIV 382

Ulwazi Lombukiso

Ulwazi Lombukiso (6)

Isitifiketi Sokuhlonishwa

Iphrofayela Yenkampani

Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokushesha yobuchwephesha be-biotechnology ekhethekile ekucwaningeni, ekuthuthukiseni, ekukhiqizeni nasekusabalaliseni amakhithi okuhlola e-in-vitro diagnostic(IVD) athuthukile namathuluzi ezokwelapha.
Indawo yethu yi-GMP, ISO9001, kanye ne-ISO13458 futhi sinemvume ye-CE FDA. Manje sesibheke ngabomvu ukubambisana nezinye izinkampani zaphesheya ukuze sithuthukiselane.
Sikhiqiza ukuhlolwa kwenzalo, ukuhlolwa kwezifo ezithathelwanayo, ukuhlola ukusetshenziswa kabi kwezidakamizwa, ukuhlola umaka wenhliziyo, ukuhlolwa komaka isimila, ukuhlolwa kokudla nokuphepha kanye nokuhlolwa kwezifo zezilwane, ngaphezu kwalokho, uhlobo lwethu lwe-TESTSEALABS lwaziwa kakhulu ezimakethe zasekhaya neziphesheya kwezilwandle. Izinga eliphezulu nezintengo ezivumayo zisenza sikwazi ukuthatha amasheya asekhaya angaphezu kuka-50%.