Uvavanyo lweFeline Leukemia i-Antign (Felv) yovavanyo
Intshayelelo
The Feline Leukemia Virus Antigen (FeLV) Rapid Test is a highly sensitive and specific test for the detection antigen to Feline Leukemia Virus in feline serum. Oluvavanyo luhambisa isantya, ukulula kunye nomgangatho wovavanyo ngexabiso eliphantsi kakhulu kunezinye iimpawu.
Iparameter
Igama lemveliso | I-Felv yovavanyo lwekhasethi |
Igama lebrand | I-Veestalalas |
PI-LE Imvelaphi | I-Hangzhou Zhejiang, China |
Ubungakanani | 3.0mm / 4.0mm |
Ifomathi | Ikhasethi |
I-Capten | I-serum |
Ukuchaneka | Ngaphezulu kwe-99% |
Isatifiketi | I-CE / ISO |
Funda Ixesha | I-10min |
Iwaranti | I-HARD yegumbi kwiinyanga ezingama-24 |
I-OEM | Iyafumaneka |
Izixhobo
• Izixhobo ezibonelelweyo
1.Test Casesette 2.droppers 3.Buffer 4.Wap
• Izixhobo ezifunekayo kodwa azibonelelwanga
- I-Timer 2. Isikhongozelo seqokelelo yokuqokelela i-3.I-PLASMA kuphela)
Inzuzo
Iziphumo ezicacileyo | Ibhodi ebonakalayo yahlulwe yangamacala amabini, kwaye iziphumo zicacile kwaye kulula ukuyifunda. |
Kulula | Funda ukusebenzisa umzuzu omnye kwaye akukho zixhobo zifunekayo. |
Itshekhi ekhawulezileyo | I-10min yeziphumo, akukho mfuneko yokulinda ixesha elide. |
Imikhombandlela yokusetyenziswa
Inkqubo yovavanyo:
1) Vumela onke amalungu e-Kice kunye nesampula yokufikelela kubushushu begumbi ngaphambi kovavanyo.
2) Yongeza i-1 yehla legazi liphela, i-serum okanye iplasma kwimodeli ye-PAYP kwaye ilinde i-30-60SPOPS.
3) Yongeza i-3DRORPS ye-buffer kwimodeli.
4) Funda iziphumo ngaphakathi kwemizuzu engama-8-10. Sukufunda emva kwemizuzu engama-20.
IUkutsala iziphumo
-Izinga (+):Ubukho bobabini "C" umgca kunye nomda "we-T", akukho ncedo lwe-T licacile okanye lungacacanga.
-Nive (-):Kuphela yi-CIC kuphela evele. Akukho mgca we-t.
-Imi:Akukho mgca wombala ubonakala kwi-CD. Akunandaba nokuba i-T LI ibonakala.
Ulwazi lomboniso
Iprofayile yekhampani
Thina, i-Chenzhou Veetachnolognology Co., I-LTD yinkampani ekhulayo ye-bitechnology ekhulelweyo ekhethekileyo ekuqhubeni, ephuhlisa, ukwenziwa kunye nokusasaza i-vit yovavanyo lwe-Vitro Diacenostic (iVD).
Indawo yethu yi-GMP, i-ISO9001, kunye neSO13458 eqinisekisiweyo kwaye sinokwamkelwa kwe-FDA. Ngoku sijonge phambili ekubambeni ngeenkampani ezingapheliyo zophuhliso.
Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, iimvavanyo zokusebenzisana iziyobisi, iimvavanyo zokumakisha i-Cardiac, iimvavanyo zokumakisha i-goumoc, iimvavanyo zokutya kwe-tumor, uvavanyo lwezifo zethu, ukongeza, iimvavanyo zethu zokutya, ukongeza kwimarike yezasekhaya. Eyona ndawo ilungeleleneyo kunye namaxabiso afanelekileyo esenza ukuba sithathe ngaphezulu kwe-50% izabelo zasekhaya.
Inkqubo yemveliso
1.Topt
2.Cover
3.cross membrane
4.Sut Strip
5.assebyly
6.Packck iipakethi
7.Feal iipakethi
8.pack ibhokisi
I-Khupha