WebAdd 3 volumes of NorthernMax buffer. The Millennium Markers need to be denatured also. Use 2ul + 6ul NorthernMax buffer. Heat at 65C for 15 minutes. IMPORTANT When this has finished, immediately move samples to ice. If samples are allowed to slowly cool, some RNAs may bind to proteins/form secondary structure and will run weird. WebJournal: Cell Article Title: Promoter of lncRNA gene PVT1 is a tumor suppressor DNA boundary element doi: 10.1016/j.cell.2024.03.068 Figure Lengend Snippet: Key Resources Table Article Snippet: After hybridization, membrane was washed twice with NorthernMax Low-Stringency Wash Solution (Thermo Fisher, Cat#AM8673) for 5 min followed by …
NorthernMax™ Prehybridization/Hybridization Buffer
WebTitle: NorthernMax Prehybridization/Hybridization Buffer AM8677 Rev. B Author: Life Technologies 05.2013 Subject: NorthernMax Prehybridization/Hybridization Buffer WebNorthernMax ™ –Gly Kit is an alternative to formaldehyde-based systems for northern analysis and uses a glyoxal/DMSO Loading Solution for sample denaturation. Sufficient … reading lha rate
NorthernMax Formaldehyde Load Dye
WebThe NorthernMax® 10X Gel Running Buffer is a MOPS-based buffer (containing sodium acetate and EDTA) for use as a running buffer in denaturing formaldehyde agarose gel … Web2. Transfer for 2 hours or more using the NorthernMax transfer buffer. 3. Cross-link RNA onto nylon using a UV crosslinker, or bake at 80°C for 30 minutes. Important: Do not touch the membrane; always handle by the corners and only with clean forceps. Fingerprints, even from a glove, will clearly show on the scanned image of the membrane. WebNorthernMax Kit berisi satu set lengkap RNase bebas reagen - termasuk agarosa berkualitas tinggi, larutan gel loading, preparasi gel dan running buffer gel, buffer transfer, penyangga hibridisasi, larutan mencuci dan RNaseZap, sebuah dekontaminasi solusi ribonuklease beracun untuk peralatan dan bekerja permukaan - untuk menjalankan … how to submit form 10e online