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While the nucleus scope always immediately follows the focus marker 是 si 7, the restrictor can precede or follow the maximality operator 都 to 1.6 For example, the restrictor, indicated by being underlined below, precedes the operator in 1 and 2 and follows it in 3. The restrictor may remain implicit, as in 4.7.
Three discriminatory amino acids (underlined below) determine DNA binding, EGCKS and EGCKG in NR2 family members and orphan NRs [1].
These interests emerged as the principal rationale for caseload midwifery, as underlined below by the chief midwife's focus on maintaining work satisfaction among caseload midwives.
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The primers used for HTS contained: 1) the adaptor sequences used for cluster generation, as specified by Illumina (see underlined sequence below, 2) a two-nucleotide barcode (NN) that was sample specific so that seven tissue-specific samples could be quantified in a single sequencing channel and 3) the common primers contained within the asMIPs.
The products showing bioaffinity are underlined in gray Below, the MS structure elucidation of two ions is discussed in detail.
Synthesize complementary oligonucleotides that contain the HIV-1 Rev NES sequence (underlined in sequence below) with overhangs compatible with Xho I, generate a Not I restriction site and maintain the reading frame after loxP recombination.
Synthesize complementary oligonucleotides that contain the HIV-1 Rev NES sequence (underlined in sequence below) with overhangs compatible with XhoI, generate a NotI restriction site and maintain the reading frame after loxP recombination.
However, three key findings are underlined in the paragraphs below.
Synthesize complementary oligonucleotides that contain a loxP site (underlined in the sequence below) and generate KpnI overhangs (Note: KpnI was chosen because it is a unique restriction site within the vector only).
Synthesize complementary oligonucleotides that contain a loxP site (underlined in the sequence below) and generate Kpn I overhangs (Note: Kpn I was chosen because it is a unique restriction site within the vector only).
Transfection was performed eighteen hours later with a siRNA designed against S100A4 RNA (siS100A4) or with a siS100A4-4 MIS bearing 4 mismatches with respect to siS100A4 (underlined in the sequence below).
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