Residual activity of VCPO, LdhA, LacZ, or GapA reversibly immobilized on Ni-NTA agarose after 300 s of plasma treatment. After plasma treatment, enzyme was eluted from the carrier with imidazole and washed with buffer. Protein concentration was determined using Bradford assay. Enzyme activity was measured using 5 µl of the eluted enzyme in its respective activity assay. Activities were normalized to the respective protein concentrations and activity of the untreated enzyme was set to 100%. Means and standard deviations represent three independent biological replicates.
Primary tabs
Figure 6 Residual activity reversibility assay
Resources
- Figure 2 HRP residual activities
- Figure 2 GapA Residual activities
- Figure 2 LacZ Residual activities
- Figure 2 LdhA Residual activity
- Figure 2 VCPO Residual activity
- Figure 3 GapA
- Figure 3 HRP
- Figure 3 LacZ
- Figure 3 LdhA
- Figure 3 VCPO
- Figure 4 Protection Factor
- Figure 5 b-e Degradation
- Figure 5a Plasma-mediated protein detachment
- Figure 6 Residual activity reversibility assay
- Suppl. Figure 2 GapA Binding efficiency
- Suppl. Figure 2 HRP Binding efficiency
- Suppl. Figure 2 LacZ Binding efficiency
- Suppl. Figure 2 LdhA Binding efficiency
- Suppl. Figure 2 VCPO Binding efficiency
Additional Information
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mimetype | application/vnd.openxmlformats-officedocument.spreadsheetml.sheet |
filesize | 29.59 KB |
resource type | file upload |
timestamp | Dec 06, 2023 |