Amashubhu wokugcina isampula: Ungazikhetha kanjani amashubhu wokugcina afanele kumasampula akho ayigugu?

Amashubhu wokugcina amasampula ahlukahlukene okusetshenziswa. Zingakwazi ukugcotshwa noma zisetshenziswe njengezithuthi / amashubhu wokugcina ezokuhamba kanye nokugcinwa kwama-reagents afana nama-oligonucleotides, ama-proteter noma ama-buffers.

Ungahlukanisa kanjani?
1️⃣ ngevolumu: 0.5ml / 1.5ML / 2ML
2️⃣ kususelwa esakhiweni esingezansi seshubhu
3️⃣ Ngokusho kokujula kwekhava yeshubhu: ukumboza okujulile kwe-tube / ishubhu lokugcina lesembozo esingajulile

Ungakukhetha Kanjani?
✅ Ukubekwa uphawu
Lesi yisidingo sekhwalithi esiyisisekelo kunazo zonke se-tube yokugcina. Ukubekwa uphawu kuqinisekiswa ikakhulukazi ngemicu eqondile nama-o-ring. Izindlela zokutholwa ezivame ukusetshenziswa ziyisivivinyo esingesihle sokuvimbela uphawu nokufakelwa kwesisindo;
✅ Ukuchithwa kanye nezulu
Lokhu kuhlobene kakhulu nezinto zokwakha ama-reagents namashubhu. Okokuqala, udinga ukukhetha ishubhu yokugcina eyenziwe ngezinto zokwakha ze-polypropylene zezokwelapha. Ngasikhathi sinye, udinga ukwenza izivivinyo zokuchithwa kanye nezivivinyo zemvula ukuqinisekisa umthelela we-Storage Tube Material ekusebenzeni nasekunqumeni kwama-reagents;
✅ Ukuhlanzeka Kwebhayoloji
Ukuhlanzeka kwemvelo kuvame ukubhekisa ukuthi ishubhu liqukethe ama-nucleases, i-DNA, ama-PCR inhibitors, ama-microorganisms, imithombo yokushisa, inzalo nezinye izinkomba nezinye izinkomba nezinye izinkomba nezinye izinkomba nezinye izinkomba. Lokhu kungenziwa ngokukhetha amashubhu wokugcina anamazinga ahlukene wekhwalithi ehlanzekile ngokwezidingo nokusetshenziswa kwama-reagents agcinwe;
✅ Ama-adsorption
Ukukhetha amashubhu wokugcina nge-DNA ephansi (i-RNA) noma ama-adsorption angu-protein angaqinisekisa ukuthi izinga lokulahleka kwesampula lincishisiwe;
✅ Igesi kanye ne-Bacterial Barrier Properties
Njengoba indawo yokugcina kanye nendawo yokuhamba yama-reagents ngokuvamile (izinga lokushisa eliphansi, iqhwa elomile, i-nitrogen elomile, njll.)