PSA Prostate Specific Antigen Test Kit
Parameter tafura
Model Number | TIN101 |
Zita | PSA Prostate Specific Antigen Qualititive Test Kit |
Features | High senitivity, Nyore, Nyore uye Yakarurama |
Muenzaniso | WB/S/P |
Tsanangudzo | 3.0mm 4.0mm |
Kururama | 99.6% |
Storage | 2'C-30'C |
Shipping | Negungwa/Nemhepo/TNT/Fedx/DHL |
Instrument classification | Kirasi II |
Chitupa | CE ISO FSC |
Sherufu hupenyu | makore maviri |
Type | Pathological Analysis Equipments |
Nheyo yeFOB Rapid Test Device
Iyo PSA Rapid Test Device (Whole Ropa) inoona maantigen eprostate kuburikidza nekududzira kwekuona kwekukura kweruvara pamutsara wemukati. PSA masoja ekudzivirira chirwere haafambike panzvimbo yekuyedza ye membrane. Panguva yekuyedzwa, mufananidzo wacho unopindirana nePSA masoja ekudzivirira chirwere akasanganiswa kune zvimedu zvine mavara uye akaiswa papepa remuenzaniso webvunzo. Musanganiswa wacho unobva watama nepakati pe membrane ne capillary action, uye inopindirana nemareagents pa membrane. Kana paine PSA yakakwana mumuenzaniso, bhendi rine ruvara richaumbwa panzvimbo yekuyedza ye membrane. Bandi rekuedza (T) singal risina simba kupfuura referensi bhendi (R) rinoratidza kuti PSA level mumuenzaniso iri pakati pe4-10 ng/mL. Chiyero bhendi (T) chiratidzo chakaenzana kana pedyo nebhendi rereferensi (R) inoratidza kuti nhanho yePSA mumuenzaniso ingangoita gumi ng/mL. Bandi rekuyedza (T) chiratidzo chakasimba kupfuura bhendi rereferenzi (R) inoratidza kuti nhanho yePSA mumuenzaniso iri pamusoro pe10 ng/mL. Kuonekwa kwebhandi remavara panzvimbo yekutonga inoshanda sekutonga kwemaitiro, zvichiratidza kuti chiyero chakakodzera chemuenzaniso chakawedzerwa uye membrane wicking yakaitika.
Iyo PSA Rapid Test Device (Ropa Rakazara/Serum/Plasma) inokurumidza kuona immunoassay yemhando yekufungidzira yeprostate chaiyo antigens muropa remunhu, serum, kana plasma mienzaniso. Iyi kit yakagadzirirwa kushandiswa seyamuro mukuongororwa kwegomarara reprostate.
Test Procedure
Huya nemiedzo, zvienzaniso, buffer uye/kana zvidzoreso kune tembiricha yemumba usati washandisa.
1. Bvisa bvunzo kubva muhomwe yayo yakavharwa, woiisa panzvimbo yakachena, yakaenzana. Nyora mudziyo nemurwere kana chitupa chekudzora. Kuti zvive nemigumisiro yakanaka, kuongorora kunofanira kuitwa mukati meawa imwe chete.
2. Tumira 1 madonhwe e serum / plasma kumuenzaniso tsime (S) yemudziyo nepipette yakapiwa inoraswa, wobva wawedzera 1 donho rebhafa, uye tanga timer.
OR
Chinja madonhwe maviri eropa rakazara kumuenzaniso mutsime (S) wemudziyo une pipette inoraswa, wobva wawedzera 1 donhwe rebuffer, wotanga timer.
OR
Bvumira madonhwe maviri akarembera echigunwe cheropa rose kuti awire pakati pemuenzaniso mugodhi (S) wemuchina wekuyedza, wobva wawedzera donhwe rimwe rebhafa, wotanga chibatiso chenguva.
Dzivisa kuteya mabhuru emhepo mumuenzaniso mutsime (S), uye usawedzera chero mhinduro kunzvimbo yemhedzisiro.
Sezvo bvunzo inotanga kushanda, ruvara rwunofamba nepakati pe membrane.
3. Mirira kuti bhendi (ma) mavara rionekwe. Chigumisiro chinofanira kuverengwa pamaminitsi gumi. Usadudzire mhinduro mushure memaminitsi makumi maviri.
ZVIRI MUKITI
Iyo PSA Rapid Test Device (Ropa Rose) inokurumidza kuona immunoassay yemhando yekufungidzira yeprostate chaiyo antigen muropa remunhu, serum, kana plasma mienzaniso. Iyi kit yakagadzirirwa kushandiswa seyamuro mukuongororwa kwegomarara reprostate.
DUDZIRIRO YEMIZVO
Zvakanaka (+)
Mabhendi e-rose-pink anoonekwa munzvimbo dzese dzekutonga uye dunhu rekuyedza. Inoratidza mhedzisiro yakanaka yehemoglobin antigen.
Negative (-)
A rose-pink bhendi inoonekwa munharaunda yekutonga. Hapana bhendi remavara rinoonekwa munzvimbo yekuyedza. Zvinotaridza kuti kuwanda kwe hemoglobin antigen i zero kana kuti pasi peyero yekuona bvunzo.
Hazvina basa
Hapana bhendi rinooneka zvachose, kana kune bhendi rinooneka chete mudunhu rekuyedza asi kwete mudunhu rekutonga. Dzokorora netest kit itsva. Kana bvunzo ichiri kutadza, ndapota taura nemugovera kana chitoro, kwawakatenga chigadzirwa, nenhamba yemujenya.
Exhibition Information
Honorary Certificate
Profile yekambani
Isu, Hangzhou Testsea Biotechnology Co., Ltd ikambani inokura nekukurumidza nyanzvi yebiotechnology nyanzvi mukutsvagisa, kugadzira, kugadzira uye kugovera epamberi in-vitro diagnostic (IVD) bvunzo kits uye zviridzwa zvekurapa.
Nzvimbo yedu ndeye GMP, ISO9001, uye ISO13458 certified uye isu tine CE FDA mvumo. Ikozvino tave kutarisira kushanda pamwe nemamwe makambani ari mhiri kwemakungwa mukusimudzirana.
Isu tinogadzira bvunzo dzekubereka, bvunzo dzezvirwere zvinotapukira, bvunzo dzekushandisa zvinodhaka, bvunzo dzemwoyo, bvunzo dze tumor marker, chikafu uye chengetedzo bvunzo uye bvunzo dzechirwere chemhuka, uyezve, mhando yedu TESTSEALABS yave ichizivikanwa mumisika yemumba neyekunze. Yakanakisa mhando uye mitengo yakanaka inoita kuti titore pamusoro pe50% migove yemumba.
Product Process
1.Gadzirira
2.Chivharo
3.Muchinjikwa membrane
4.Cheka tambo
5.Assembly
6.Pack the pouches
7.Sima zvikwama
8.Pack bhokisi
9.Encasement