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To evaluate for protein loading, the PVDF membrane was stripped (Reblot Plus Mild; Millipore, Billerica, MA, USA) and incubated with anti-actin antibody (1 10 000; Sigma) in 5% (w/v) BSA for an hour at room temperature and then processed as described above (secondary antibody: HRP conjugated anti-chicken immunoglobulin 1 100 000 in 5% BSA; Sigma).
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Sequence predictions were evaluated for protein sequences, text data, music files etc. Route prediction is not covered by this work.
The protein isolates were evaluated for protein extraction yield, protein solubility, heat stability and nutritional properties (chemical score, digestibility, PDCAAS).
Furthermore, the designed formulation was evaluated for protein adsorption, hemo˗cytocompatibility and stability.
If a lumbar puncture was performed, cerebral spinal fluid was evaluated for protein and cell counts.
Transgenic cassava events with low (1 to 2) copy number, high RNA expression and high protein content were propagated and transferred to soil in 7 cm pots grown in the greenhouse, and evaluated for protein accumulation.
Samples were powdered and evaluated for protein, fat, carbohydrates, ash, and crude fibres.
Supernatants from murine splenocytes treated with CII were evaluated for protein expression.
By immunohistochemical analysis, 137 different primary melanomas could be evaluated for protein expression of FGFR4.
Whole-cell extracts from NSCLC and PDAC cells were evaluated for protein content by western blot.
A first-generation targeting system with a single recombinase target site has recently been evaluated for protein production.
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CEO of Professional Science Editing for Scientists @ prosciediting.com