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Exact(7)
Cell-free extracts (60 µg protein) were loaded on 12% 1-D SDS PAGE (Invitrogen) and resolved proteins from several mini-gels were transferred to the same PVDF membrane (Millipore) so that one set of samples was used to monitor protein loading using β-Actin.
HSC70 was used to monitor protein loading.
The same blot was reprobed for β-actin to monitor protein loading on the blot.
Blots were stripped and reprobed with a β-actin antibody to monitor protein loading.
To monitor protein loading, actin levels were determined using mouse anti-actin mAb C4 (ICN Biomedicals, Aurora, OH).
Whole cell lysates were analysed by SDS-11% PAGE and immunoblot analysis as above, using anti-HA to detect T3S translocated ExoS effectors, anti-RalA to assess T3S translocated ExoS-ADPRT activity, and anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) (Millipore, Temecula CA) to monitor protein loading of whole cell lysates.
Similar(53)
Mouse anti-GAPDH antibody was used to monitor equal protein loading.
Ponceau staining was used to monitor equal protein loading and transfer.
Ponceau staining of membranes was used to monitor protein transfer and loading.
Differences in protein loading were monitored by probing membranes with monoclonal anti-α-Tubulin antibody.
Protein loading was monitored using a mouse monoclonal antibody against β-actin (1 30 000, Sigma-Aldrich).
Related(20)
control protein loading
monitor protein transfer
monitor protein S-glutathionylation
monitor protein distribution
monitor protein kinase
monitor protein translation
monitor protein backbone
monitor protein conformation
monitor protein binding
monitor protein synthesis
monitor protein localization
monitor protein oxidation
monitor protein quality
monitor protein adsorption
monitor protein modification
monitor protein expression
monitor protein variation
monitor protein folding
monitor protein stability
monitor protein aggregation
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