Labshake search
Citations for Promega :
501 - 550 of 1206 citations for L Aspartic Acid N T Boc B Bz Ester 13C4 97 99%; 15N 97 99% since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
-
bioRxiv - Evolutionary Biology 2019Quote: ... The purified PCR products were ligated with the pGEM®-T vector (Promega) as recommended by the manufacturer and subsequently sequenced (Macrogen) ...
-
bioRxiv - Cell Biology 2019Quote: ... targeted DNA regions were amplified and respective amplicons cloned into pGEM-T (Promega) and the products subjected to Sanger sequencing ...
-
bioRxiv - Microbiology 2020Quote: ... The amplicon was cloned into the pGEM-T Easy vector (Promega, Madison, WI) and then subcloned into the pQE80 expression vector (Qiagen ...
-
bioRxiv - Evolutionary Biology 2021Quote: ... The products were then cloned into the pGEM-T Easy Vector System (Promega) and sequenced them on an ABI 3730 sequencer from both directions using T7 forward and M13 reverse primers ...
-
bioRxiv - Evolutionary Biology 2021Quote: ... The amplified products were cloned into the pGEM®-T Easy vector (Promega). Plasmids were extracted and purified using a TIANprep Mini Plasmid Kit II (Tiangen) ...
-
bioRxiv - Cancer Biology 2020Quote: ... and used to ligate into pGEM®-T Easy Vector System (Promega #A1360) at room temperature for 60 m using the manufacturer’s suggested protocol ...
-
bioRxiv - Evolutionary Biology 2021Quote: ... Probes were synthesized from cDNAs cloned into the pGEM®-T Easy (Promega) plasmid ...
-
bioRxiv - Molecular Biology 2021Quote: ... The amplified fragment was cloned into pGEM®-T Easy vector (Promega, USA) and sequenced ...
-
bioRxiv - Developmental Biology 2020Quote: ... the pcr product was cloned into pGEM®-T Easy Vector Systems (Promega) and sequence was analyzed after sanger sequencing ...
-
bioRxiv - Cancer Biology 2020Quote: ... PCR products were cloned into the pGEM-T Easy vector (Promega, Cat. A1360) and submitted to Sanger sequencing.
-
bioRxiv - Molecular Biology 2022Quote: ... 7 and 10 were either cloned with the pGEM®-T kit (Promega) to assay individual sequences and/or sequenced by Illumina (Centre d’expertises et de services Genome Québec) ...
-
bioRxiv - Bioengineering 2022Quote: ... PCR product was purified and ligated to the pGEM®-T vector (Promega). The construction was transformed into NEB® Turbo competent E ...
-
bioRxiv - Developmental Biology 2022Quote: ... PCR products were cloned into the pGEM-T Easy vector (Promega, Madison, WI). Linearized template DNA (amplified from plasmid with T7/SP6 primers ...
-
bioRxiv - Microbiology 2022Quote: ... The 1,260 bp amplicon was ligated into pGEM-T Easy (Promega, Madison, WI), and propagated in E ...
-
bioRxiv - Molecular Biology 2022Quote: ... a fragment of the pGEM®-T Easy vector (Promega, Madison, WI, USA) was spiked into the cytosolic fraction according to the protein concentration ...
-
bioRxiv - Molecular Biology 2023Quote: ... PCR products were sub cloned into the pGEM-T-Easy vector (Promega, A1360) using manufactures instructions ...
-
bioRxiv - Developmental Biology 2023Quote: ... Cloned gene fragments were inserted into the pGEM-T Easy vector (Promega, A1360) and transformed into One Shot Top 10 chemically competent E ...
-
bioRxiv - Cell Biology 2023Quote: ... The PCR products were cloned in the pGEM T Easy vector system (Promega) according to the manufacturer’s instructions and sequenced (Eurofins Genomics and SourceBioscience) ...
-
bioRxiv - Molecular Biology 2023Quote: ... The full-length cDNA was ligated into the pGEM T-Easy vector (Promega) and sequenced using Sanger’s method to confirm the specificity of the product ...
-
bioRxiv - Molecular Biology 2023Quote: ... The amplified product was then cloned into the pGEM T-Easy Vector (Promega) and subjected to Sanger sequencing ...
-
bioRxiv - Biophysics 2023Quote: ... Purified DNA fragments were ligated into the pGEM®t-easy plasmid (Promega) and transformed into DH5α bacteria selected on standard Luria broth (LB ...
-
bioRxiv - Plant Biology 2023Quote: ... The PCR product was first cloned in the pGEM-T Easy vector (Promega) and sequenced ...
-
bioRxiv - Molecular Biology 2024Quote: ... 25,000 HEK293-T cells were seeded and transfected with FuGENE 6 (#E231A, Promega) and plasmid DNA at the carrier (µL):DNA (µg ...
-
bioRxiv - Plant Biology 2024Quote: ... The resulting bands were gel purified and cloned into pGEM T-easy (Promega) and sent out for Sanger sequencing.
-
bioRxiv - Cell Biology 2024Quote: ... PCR products were sub-cloned into the pGEM-T Easy vector (Promega, A1360) and sequenced ...
-
bioRxiv - Plant Biology 2023Quote: ... The DNA fragments were subcloned into the pGEM®-T Easy Vector (Promega) and checked by sequencing ...
-
bioRxiv - Neuroscience 2023Quote: The PCR fragment were ligated into a pGEM-T Easy Vector System (Promega), transformed into chemically competent cells and sequenced ...
-
bioRxiv - Microbiology 2023Quote: ... Nucleic acid was recovered using the Maxwell RSC instrument (Promega). After DNAse treatment and elution ...
-
bioRxiv - Synthetic Biology 2021Quote: ... We also included N-terminal and C-terminal HiBiT tags (Promega, Madison, WI) for quantification using luminescence ...
-
bioRxiv - Molecular Biology 2020Quote: ... Cells were transfected with NOCT N-terminal mutant constructs using Fugene HD (Promega) in a ratio of 3 µL transfection reagent per 1 µg DNA ...
-
bioRxiv - Molecular Biology 2023Quote: ... HiBiT fusion vectors were constructed using the parental vector pBiT3.1-N (N2361, Promega). To generate the HiBiT-VHL vector ...
-
bioRxiv - Molecular Biology 2023Quote: ... NanoLuc fusion vectors were constructed using the parental vectors pNLF1-N (N1351, Promega) and pNLF1-C (N1361 ...
-
bioRxiv - Cancer Biology 2021Quote: ... Cells that showed indels were then cloned into the pGEM-T Easy vector (Promega), and colonies were picked using blue/white screening then sequenced ...
-
bioRxiv - Immunology 2021Quote: ... The PCR products were inserted into the pGEM-T Easy Vector System (Promega, A1360) following the manufacturer’s instructions ...
-
bioRxiv - Microbiology 2020Quote: ... A-tailed PCR amplicons were cloned into p-GEM-T Easy Vector System (Promega) per manufacturer instructions and ligation reactions introduced directly into electrocompetent XL1-Blue E ...
-
bioRxiv - Developmental Biology 2019Quote: ... PCR products were purified and cloned into a pGEM-T Easy vector (Promega, USA) according to the manufacturer’s instruction and the identity of inserts confirmed by sequencing.
-
bioRxiv - Evolutionary Biology 2019Quote: ... PCR products were purified and cloned into a pGEM-T Easy vector (Promega, USA) according to the manufacturer’ s instruction and the identity of inserts confirmed by sequencing ...
-
bioRxiv - Evolutionary Biology 2021Quote: ... The synthesized cDNA was inserted into a pGEM-T Easy vector (Promega, Madison, WI) and the full length was verified by sequencing.
-
bioRxiv - Neuroscience 2020Quote: Purified PCR fragments were cloned into a pGEM-T Easy Vector (Promega, Madison, Wisconsin), according to the manufacturer’s protocol ...
-
bioRxiv - Plant Biology 2022Quote: ... The amplicons were subcloned using pGEM-T Easy Vector Systems Kit (Promega, Tokyo, Japan) or Zero Blunt PCR Cloning Kit (Thermo Fisher Scientific ...
-
bioRxiv - Developmental Biology 2020Quote: Whole open reading frame of eco1 and eco2 where cloned into pGEM-T (Promega). DIG-labeled probes where generated using T7/SP6 transcriptions start sites and the digoxigenin RNA Labeling Mix kit (Roche ...
-
bioRxiv - Immunology 2020Quote: ... The A-tailed products were subsequently cloned into pGEM®-T Easy vector (Promega) using the manufacturer’s protocol ...
-
bioRxiv - Cancer Biology 2022Quote: ... Amplified genomic DNA fragments were cloned into the pGEM-T Easy vector (Promega, USA) and sequenced ...
-
bioRxiv - Plant Biology 2019Quote: ... Each purified fragment was cloned into pGEM-T Easy Vector (Promega, Madison, WI, USA) following the manufacturer’s protocol ...
-
bioRxiv - Developmental Biology 2019Quote: ... and products were cloned into the pGEM-T Easy vector (Promega, Madison, WI, A1360). In vitro transcription was performed with SP6 or T7 RNA polymerase (Roche ...
-
bioRxiv - Microbiology 2019Quote: ... The reaction mixtures were then ligated into pGEM-T Easy vector (Promega Catlog#A1360) overnight at 4°C and then transformed into TOP10 competent E ...
-
bioRxiv - Cell Biology 2021Quote: PCR fragments were cloned into the pGEM-T Easy plasmid (Promega Corporation, Madison WI) under the conditions established by the manufacturers and E ...
-
bioRxiv - Physiology 2020Quote: ... and products were ligated into the pGEM-T Easy vector (Promega Madison, Wisconsin, USA). The inserts were digested from the pGEM-T Easy vector and directionally cloned into the expression vector ...
-
bioRxiv - Molecular Biology 2021Quote: ... probes listed in Supplementary Table 7 were cloned in pGEM®-T Easy (Promega) for T7 polymerase transcription.
-
bioRxiv - Cancer Biology 2020Quote: ... The Alu PCR product was cloned into using pGEM-T Easy Vector (A1380, Promega). The clones obtained were subjected to Sanger sequencing for verification ...