Your English writing platform
Discover LudwigSuggestions(1)
Similar(60)
PU.1 DNA binding was adjusted to Oct-1 DNA binding.
Extracts for binding reactions were adjusted to 1X binding buffer and 0.5 μg/μl tRNA, and pretreated with buffer-washed beads (200 μl of plastid extract to 50 μl beads) prior to use in binding reactions (beads used for this pretreatment were discarded).
Binding reactions were adjusted to the following final conditions: 10 mM HEPES (pH 7.5), 100 mM KCl, 3 mM DTT, 0.05% NP-40, 3% glycerol, 5 μg/ml BSA, 2.5 mM MgCl2 and 5 μM ZnCl2.
The binding sites defined for docking were adjusted to be similar to the Surflex protomol.
qRT-PCR data were adjusted to TATA-box-binding protein (TBP) mRNA levels.
For apoptosis analysis, cells were adjusted to a density of 1 × 10/mL with binding buffer.
Mature parasitized RBCs were adjusted to 5 20% parasitemia and 0.5 1% hematocrit by the addition of nonparasitized RBCs in binding media (BM; RPMI-1640, 0.5% BSA, pH 6.7).
Cells were adjusted to 105/ml.
FRAP values were adjusted to monoexponential fitting.
The binding buffer was adjusted to remove all unincorporated primers according to the manufacturer's recommendation.
As kinetic binding experiments revealed that approximate equilibrium was reached after a 3 h incubation period with scFv (6 C and D), the incubation time for binding studies was adjusted to this incubation time.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com