Selected article for: "µg ml and lysis buffer"

Author: Prashali Bansal; Johannes Madlung; Kristina Schaaf; Boris Macek; Fulvia Bono
Title: An interaction network of RNA-binding proteins involved in Drosophila oogenesis
  • Document date: 2020_1_9
  • ID: 2f9nc2to_4
    Snippet: Lysates were cleared by centrifugation at 21,000g for 20 min at 4 ºC and 5 µl/ml of RNase A/T1 (Thermo Fisher Scientific) was added to the supernatants. After incubation at 4 ºC for 30 min, lysates were cleared again and 30-60 µl of GFP-TRAP MA beads (Chromotek) were added. The mixtures were incubated for 1 hour at 4 ºC in rotation. Beads were washed with lysis buffer and proteins were eluted as described above......
    Document: Lysates were cleared by centrifugation at 21,000g for 20 min at 4 ºC and 5 µl/ml of RNase A/T1 (Thermo Fisher Scientific) was added to the supernatants. After incubation at 4 ºC for 30 min, lysates were cleared again and 30-60 µl of GFP-TRAP MA beads (Chromotek) were added. The mixtures were incubated for 1 hour at 4 ºC in rotation. Beads were washed with lysis buffer and proteins were eluted as described above.

    Search related documents:
    Co phrase search for related documents
    • lysate clear and lysis buffer: 1
    • lysis buffer and protein lysis buffer: 1, 2, 3, 4, 5