PSA Prostate Specific Antigen Test Kit

Inkcazelo emfutshane:

UVavanyo oluKhawulezayo lwe-PSA luvavanyo lwe-immunochromatographic lokufumanisa umgangatho we-Prostate Specific Antigen (PSA) kwiserum yomntu okanye i-plasma specimen.Yenzelwe ukuba isetyenziswe njengovavanyo lokuhlola kwaye njengoncedo ekuxilongeni umhlaza wesinyi.

Uvakalelo oluchanekileyo oluphezulu kunye neenkcukacha zokuchongwa kwe-Prostate Specific Antigen (PSA) kwi-serum yabantu okanye iplasma.

Thumela i-imeyile kuthi Khuphela njengePDF

Iinkcukacha zeMveliso

Iithegi zeMveliso

Itheyibhile yeParameter

Inombolo yoMzekelo	I-TSIN101
Igama	I-PSA Prostate Specific Antigen Qualititive Test Kit
Iimbonakalo	Uvakalelo oluphezulu, lulula, lulula kwaye luchanekile
Umzekelo	WB/S/P
Inkcazo	3.0mm 4.0mm
Ukuchaneka	99.6%
Ugcino	2'C-30'C
Ukuhambisa ngenqanawe	Ngolwandle/Ngomoya/TNT/Fedx/DHL
Ukuhlelwa kwesixhobo	Udidi II
Isatifikethi	CE ISO FSC
Beka ubomi kwishelufa	iminyaka emibini
Uhlobo	Izixhobo zokuHlalutya kwePathological

HIV 382

Umgaqo we-FOB Rapid Test Device

I-PSA Rapid Test Device (Igazi Elipheleleyo) ibona i-antigens ethile ye-prostate ngokuchazwa okubonakalayo kokuphuhliswa kombala kumgca wangaphakathi.Izilwa-buhlungu ze-PSA azishukumi kwindawo yovavanyo yenwebu.Ngexesha lovavanyo, isampuli iphendula kunye ne-PSA antibodies edityaniswe kumasuntswana anemibala kwaye yafakwa ngaphambili kwisampulu yovavanyo.Umxube ke ufuduka kwi-membrane ngesenzo se-capillary, kwaye udibanise ne-reagents kwi-membrane.Ukuba kukho i-PSA eyaneleyo kwi-specimen, ibhendi enemibala iya kwenza kwindawo yokuvavanya ye-membrane.Ibhendi yovavanyo (T) i-singal ibuthathaka kunebhendi yereferensi (R) ibonisa ukuba inqanaba le-PSA kwi-specimen liphakathi kwe-4-10 ng / mL.Ibhendi yovavanyo (T) isignali elinganayo okanye ekufutshane nebhendi yereferensi (R) ibonisa ukuba inqanaba lePSA kumzekelo limalunga ne-10 ng/mL.Ibhendi yovavanyo (T) isibonakaliso esinamandla kunebhendi yereferensi (R) ibonisa ukuba inqanaba le-PSA kwi-specimen lingaphezulu kwe-10 ng / mL.Ukubonakala kwebhanti enemibala kwindawo yokulawula isebenza njengolawulo lwenkqubo, ebonisa ukuba umthamo ofanelekileyo we-specimen wongeziwe kwaye i-membrane wicking yenzeke.

Isixhobo soVavanyo oluKhawulezayo lwe-PSA (iGazi eliPheleleyo/iSerum/i-Plasma) luvavanyo olukhawulezayo olubonakalayo lokujonga ukubonwa kwe-prostate ethile ye-antigens kwigazi elipheleleyo lomntu, i-serum, okanye i-plasma specimens.Le khithi yenzelwe ukusetyenziswa njengoncedo ekuxilongeni umhlaza wesinyi.

HIV 382

Inkqubo yoVavanyo

Zisa iimvavanyo, imizekelo, isithinteli kunye/okanye ulawulo kwiqondo lobushushu begumbi phambi kokusetyenziswa.

1. Susa uvavanyo kwisingxobo salo esitywiniweyo, kwaye ulubeke kwindawo ecocekileyo, esemgangathweni.Faka ileyibhile kwisixhobo ngesazisi sesigulane okanye solawulo.Ukuze ufumane iziphumo ezingcono, uvavanyo kufuneka lwenziwe kwiyure enye.

2. Dlulisa i-1 ithontsi ye-serum / i-plasma kwi-specimen well (S) yesixhobo kunye ne-pipette enikeziweyo elahlayo, uze udibanise i-1 drop of buffer, kwaye uqale isibali-xesha.
OR
Dlulisa ama-2 amathontsi egazi elipheleleyo kwi-specimen well (S) yesixhobo kunye ne-pipette enikezelwayo, uze udibanise i-1 drop of buffer, kwaye uqalise isibali-xesha.
OR
Vumela amathontsi ama-2 ajingayo entonga yeminwe yegazi elipheleleyo ukuba awele embindini wequla lomzekelo (S) wesixhobo sovavanyo, emva koko wongeze ithontsi enye yesithinteli, kwaye uqalise isibali-xesha.
Gwema ukubambisa amaqamza omoya kwi-specimen kakuhle (S), kwaye ungafaki nasiphi na isisombululo kwindawo yesiphumo.
Njengoko uvavanyo luqala ukusebenza, umbala uya kufuduka kwi-membrane.

3. Linda ukuba i(ama)bhanti enemibala ivele.Isiphumo kufuneka sifundwe ngemizuzu eyi-10.Musa ukutolika umphumo emva kwemizuzu engama-20.

UMONGO WEKHITHI

Isixhobo soVavanyo oluKhawulezayo lwe-PSA (iGazi eliPheleleyo) luvavanyo olukhawulezayo olubonakalayo lovavanyo lokujonga umgangatho we-prostate ethile ye-antigens kwigazi elipheleleyo lomntu, i-serum, okanye i-plasma specimens.Le khithi yenzelwe ukusetyenziswa njengoncedo ekuxilongeni umhlaza wesinyi.

HIV 382

UKUTOLIKWA KWEZIPHUMO

Okuhle (+)

Iibhendi ze-rose-pink zibonakala kwindawo yokulawula kunye nommandla wokuvavanya.Ibonisa umphumo omuhle we-hemoglobin antigen.

Engalunganga (-)

Ibhendi ye-rose-pink ibonakala kwindawo yokulawula.Akukho bhanti yombala ibonakala kwindawo yovavanyo.Ibonisa ukuba i-concentration ye-hemoglobin antigen i-zero okanye ingaphantsi komda wokufumanisa uvavanyo.

Ayisebenzi

Akukho bhendi ebonakalayo kwaphela, okanye kukho ibhendi ebonakalayo kuphela kwindawo yokuvavanya kodwa kungekhona kummandla wokulawula.Phinda ngekhithi yovavanyo entsha.Ukuba uvavanyo lusasilela, nceda uqhagamshelane nomthengisi okanye ivenkile, apho uthenge imveliso, kunye nenombolo yeqashiso.

HIV 382

Ulwazi Lomboniso

Ulwazi ngomboniso (6)

Isatifikethi sembeko

Iprofayile yekhampani

Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokukhawuleza yobuchwephesha bebhayoloji ekhethekileyo ekuphandeni, ekuphuhliseni, ekuveliseni nasekusasazeni iikhithi zovavanyo lwe-in-vitro diagnostic (IVD) kunye nezixhobo zonyango.
Indawo yethu yi-GMP, ISO9001, kunye ne-ISO13458 eqinisekisiweyo kwaye sinemvume ye-CE FDA.Ngoku sijonge phambili ekusebenzisaneni neenkampani zaphesheya kwezilwandle ngophuhliso olufanayo.
Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, uvavanyo lokusetyenziswa kakubi kweziyobisi, uvavanyo lwentliziyo, uvavanyo lokumakisha ithumba, uvavanyo lokutya kunye nokhuseleko kunye novavanyo lwezifo zezilwanyana, ukongezelela, uphawu lwethu lwe-TESTSEALABS luye lwaziwa kakhulu kwiimarike zasekhaya naphesheya.Umgangatho ogqwesileyo kunye namaxabiso ancomekayo asenza sikwazi ukuthatha ngaphezulu kwe-50% yezabelo zasekhaya.