CEA Carcinoembryonic Antigen Test Kit
Table ya parameter
| Nambala ya Model | Mtengo wa TIN101 |
| Dzina | AFP Alpha-Fetoprotein Test Kit |
| Mawonekedwe | Kuzindikira kwakukulu, kosavuta, kosavuta komanso kolondola |
| Chitsanzo | WB/S/P |
| Kufotokozera | 3.0mm 4.0mm |
| Kulondola | 99.6% |
| Kusungirako | 2'C-30'C |
| Manyamulidwe | Ndi nyanja/Ndi mpweya/TNT/Fedx/DHL |
| Gulu la zida | Kalasi II |
| Satifiketi | CE ISO FSC |
| Alumali moyo | zaka ziwiri |
| Mtundu | Zida Zowunikira Pathological |
Mfundo ya FOB Rapid Test Device
CEA Rapid Test Device (Whole Blood/Serum/Plasma) idapangidwa kuti izizindikirira human carcinoembryonic antigen (CEA) kudzera mu kutanthauzira kowonekera kwa kakulidwe kamitundu mumzere wamkati. Nembanembayo inali yosasunthika ndi ma antibodies a anti-CEA pagawo loyesa. Pakuyesa, chitsanzocho chimaloledwa kuchitapo kanthu ndi anti-CEA monoclonal antibodies colloidal gold conjugates, omwe anali atayikidwa kale pachitsanzo cha mayeso. Kusakaniza ndiye kumayenda pa nembanemba ndi capillary kanthu, ndi kucheza ndi reagents pa nembanemba. Ngati panali CEA yokwanira m'zitsanzo, gulu lamitundu lidzapanga pagawo loyesa la nembanemba. Kukhalapo kwa gulu lachikudali kumasonyeza zotsatira zabwino, pamene kusowa kwake kumasonyeza zotsatira zoipa. Kuwonekera kwa gulu lachikuda pachigawo cholamulira kumagwira ntchito ngati njira yoyendetsera. Izi zikuwonetsa kuti kuchuluka koyenera kwa sampuli kwawonjezeredwa ndipo kupukuta kwa membrane kwachitika.
1.Musatsegule thumba la zojambulazo mpaka mutakonzeka kuyamba kuyesa. Zida zoyezera m'firiji ziyenera kuloledwa kuti zifike kutentha (15 ° - 28 ° C) musanatsegule thumba.
2.Chotsani chipangizocho m'thumba lachitetezo ndikulembera chipangizocho ndi chizindikiro cha chitsanzo.
3. Onjezani 50 ul ya magazi atsopano ku Chitsime Chachitsanzo (cha Khadi) kapena Padi Yachitsanzo (ya Dipstick),Kenaka onjezerani madontho awiri (50 ul) a mayeso omwe akuyendetsa nkhokwe mu chitsime cha chitsanzo kapena pad chitsanzo.
4. Werengani zotsatira mkati mwa mphindi 10- 15. Osawerenga zotsatira pakadutsa mphindi 15. Yang'anani
gulu lachikuda lomwe linapangidwa pamwamba pa dera lolamulira likuwonetsa kuti kuyesa kwatha.
Njira Yoyesera
ZOTSATIRA ZA KIT
1.Zipangizo zoyeserera pawokha
Chida chilichonse chimakhala ndi mzere wokhala ndi ma conjugates achikuda ndi ma reagents okhazikika omwe adafalikira m'magawo ofananirako.
2.Ma pipette otayika
Kuwonjezera zitsanzo ntchito.
3.Bafa
Phosphate saline wothira mchere komanso woteteza.
4.Ikani phukusi
Pakuti malangizo ntchito.
KUMASULIRIDWA KWA ZOTSATIRA
Zabwino (+)
Magulu awiri a pinki amawonekera pagawo loyesa. Izi zikuwonetsa kuti chitsanzocho chili ndi CEA
Zoipa (-)
Gulu limodzi lokha la pinki limapezeka pagawo loyeserera. Izi zikuwonetsa kuti palibe CEA m'magazi onse.
Zosalondola
Ngati popanda gulu lachikuda likuwonekera pagawo loyesa, ichi ndi chisonyezero cha zolakwika zomwe zingatheke poyesa. Kuyesera kubwerezedwa pogwiritsa ntchito chipangizo chatsopano.
Zambiri Zowonetsera
Satifiketi Yolemekezeka
Mbiri Yakampani
Ife, Hangzhou Testsea Biotechnology Co., Ltd ndi kampani yomwe ikukula mwachangu yaukadaulo yazachilengedwe yomwe imagwira ntchito kwambiri pakufufuza, kupanga, kupanga ndi kugawa zida zoyeserera za in-vitro diagnostic(IVD) ndi zida zamankhwala.
Malo athu ndi GMP, ISO9001, ndi ISO13458 ovomerezeka ndipo tili ndi chilolezo cha CE FDA. Tsopano tikuyembekezera kugwirizana ndi makampani ambiri akunja kwa chitukuko.
Timapanga mayeso a chonde, mayeso a matenda opatsirana, kuyesa kugwiritsa ntchito mankhwala osokoneza bongo, kuyesa kwa mtima, zoyesa zotupa, kuyesa kwa chakudya ndi chitetezo ndi mayeso a matenda a nyama, kuphatikizanso, mtundu wathu wa TESTSEALABS wadziwika bwino m'misika yapakhomo ndi yakunja. Mitengo yabwino kwambiri komanso mitengo yabwino imatithandiza kutenga 50% ya magawo apakhomo.
Product Process
1.Konzekerani
2.Chophimba
3. Mtanda wodutsa
4. Dulani mzere
5. Msonkhano
6.Pakani matumba
7. Tsekani matumbawo
8.Pakani bokosi
9.Encasement
