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Genomic DNA (gDNA) was extracted from the foot of one adult mussel using a standard phenol/chloroform method [ 25].
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HA and β-TCP were extracted from mussel shells using a microwave irradiation method.
Nano-crystalline hydroxyapatite (HA, Ca10(PO4)6(OH)2) was produced from waste mussel shells using a rapid microwave irradiation method.
The procedure was used to measure spirolides in mussel samples using an extraction and clean up protocol suitable for the FP assay.
Here, adhesion and molecular interaction mechanisms of Mytilus californianus foot protein-1 (mcfp-1) from California blue mussel were investigated using a surface forces apparatus (SFA) in buffer solutions of different ionic concentrations (0.2 0.7 M) and pHs (3.0 5.5).
The analysis of populations located at both extremities of the mussel range by using a multilocus approach indicated that the divergence started more than half a million years ago and that gene flow occurs or has occurred, although mainly asymmetrically from B. azoricus to B. puteoserpentis.
SCCPs mixture was used to fortify the samples of freeze-dried mussel used during the optimization of the sample preparation conditions.
Therefore, the total number of zebra mussel used for each treatment is 6 × 4 = 24.
Critical shear velocity (u⁎), erosion rates and particle size distributions of resuspended sediment were measured at two sites; an impacted muddy site with extensive mussel culture (site 1), and a coarser sandier site with less mussel influence (site 2), using a new method for assessing sediment erosion at Tracadie Bay, Prince Edward Island in August 2003.
Fluorescent cells were sorted directly into Trizol LS reagent (Life Technologies) containing 40 μg/ml mussel glycogen (Sigma-Aldrich) using a FACSAria I cell sorter (BD Biosciences).
Remove the mussel from its shell, using a fork.
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