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Genomic DNA was extracted from peripheral EDTA-treated anti-coagulated blood using a standard protocol.
DNA was extracted from EDTA whole blood using a standard phenol-based organic deproteinisation procedure [19].
High molecular weight DNA was isolated from both tumor and peripheral blood using a standard phenol-chloroform procedure.
PYGM gene was sequenced as follows: DNA was isolated from whole blood using a standard phenol-chloroform method (Nucleon BACC-2, GE healthcare Europe GMBH, Chalfont St. Giles, UK).
Genomic DNA was extracted from the peripheral blood using a standard methodology.
DNA was extracted from EDTA-treated whole blood using a standard method.
Similar(37)
Blood gas tensions, hemoglobin concentrations, and acid-base balances were determined in arterial and mixed venous blood samples using a standard blood gas analyzer (ABL 800 Flex; Radiometer, Copenhagen, Denmark).
Genomic DNA was extracted from 4 - 6 ml of peripheral blood using a modified version of the standard salting out method [ 29].
Either registered nurses or blood pressure technicians measured blood pressure using a standard mercury sphygmomanometer.
Genomic DNA from bearded collies and giant schnauzers was extracted from 200 µl EDTA blood by using a standard salt extraction protocol, the Qiagen QIAamp DNA Blood Mini Kit (Qiagen, Valencia, CA).
Genomic DNA was extracted from EDTA-treated peripheral blood sample using a standard procedure.
More suggestions(15)
blood using a FITC-conjugated
blood using a conventional
blood using a central
blood using a Quantibrite
blood using a commercial
blood using a recombinant
blood using a QIAamp
blood using a salt-based
blood using a DNeasy
blood following a standard
blood using a thin
blood using a commercialized
blood using a defibrinated
blood using a sensitive
blood using a real-time
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