Labshake search
Citations for Beckman :
301 - 350 of 569 citations for Parvalbumin PVALB cDNA ORF Clone Mouse N His tag since 2020
Citations are collected from bioRxiv only, the total number of publications could be much larger.
-
bioRxiv - Microbiology 2024Quote: ... The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and analyzed by capillary electrophoresis ...
-
bioRxiv - Microbiology 2024Quote: ... The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and analyzed by capillary electrophoresis ...
-
The RNA-binding protein RbpB is a central regulator of polysaccharide utilization in gut BacteroidesbioRxiv - Microbiology 2023Quote: ... Amplified cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics). For sequencing ...
-
bioRxiv - Immunology 2024Quote: ... Resulting cDNA was purification using Agencourt AMPure XP beads (Beckman Coulter, Indianapolis IN). Barcode index was added using a universal and index-specific primer with PCR to each ligated cDNA sample and the amplified library was enriched by AMPure XP beads purification.
-
bioRxiv - Microbiology 2023Quote: ... The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and was analyzed by capillary electrophoresis ...
-
bioRxiv - Molecular Biology 2022Quote: ... Resultant cDNA was purified using 0.8X AMPure XP beads (Beckman Coulter, CA, USA) and eluted in 42μl of nuclease-free water (KIT) ...
-
bioRxiv - Genomics 2023Quote: ... The first-strand cDNA was purified using SPRIselect beads (Beckman Coulter, Brea, CA) and purified cDNA was amplified into RNA-seq libraries by PCR with 15 cycles ...
-
bioRxiv - Neuroscience 2023Quote: ... After purification of double-stranded cDNA with 1.8× SPRISelect Beads (#B23318, Beckman Coulter), purified cDNA was eluted in 50□μl 0.1× TE buffer and subjected to end prep ...
-
bioRxiv - Genomics 2023Quote: ... After purification of double-stranded cDNA with 1.8× SPRISelect Beads (#B23318, Beckman Coulter), purified cDNA was eluted in 50Lμl 0.1× TE buffer and subjected to end prep ...
-
bioRxiv - Cell Biology 2023Quote: ... cDNA libraries were then size-selected using AMpure XP beads (Beckman Coulter #A63881). These final indexed cDNA libraries were quantified ...
-
bioRxiv - Microbiology 2024Quote: ... The cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and analyzed by capillary electrophoresis ...
-
bioRxiv - Molecular Biology 2024Quote: ... The cDNAs were purified using Agencourt AMPure XP beads (Beckman Coulter™, A63880), circularised and linearised by PCR amplification ...
-
bioRxiv - Plant Biology 2024Quote: ... Approximately 200 bp of cDNA was purified using AMPure XP beads (Beckman Coulter) and treated with 3 μL of USER Enzyme (NEB ...
-
bioRxiv - Immunology 2024Quote: ... cDNA product was purified using 1.0X AMPURE XP DNA purification beads (Beckman Coulter).
-
bioRxiv - Genomics 2024Quote: ... the cDNA and libraries were purified using AMPure XP beads (Agencourt, Beckman Coulter). We quantified the libraries using a Qubit Fluorometer 3.0 (Life Technologies ...
-
bioRxiv - Cancer Biology 2024Quote: ... The amplified cDNA was then purified using AMPure XP beads (Beckman Coulter, USA). cDNA was quantified using the Qubit dsDNA HS Assay (Thermo Fisher Scientific ...
-
bioRxiv - Cell Biology 2024Quote: ... Samples were then separated by a centrifugation at 40,000 rpm (TLA-55 angle rotor S/N 19U1568 in Beckman Coulter Optima Max XP Ultra Centrifuge ...
-
bioRxiv - Immunology 2021Quote: ... and fluorescent anti-p24 MAb (phycoerythrin [PE]-conjugated anti-p24, clone KC57; Beckman Coulter/Immunotech). The percentage of infected cells (p24+ ...
-
bioRxiv - Microbiology 2021Quote: ... and fluorescent anti-p24 MAb (phycoerythrin [PE]-conjugated anti-p24, clone KC57; Beckman Coulter/Immunotech). The percentage of infected cells (p24+ ...
-
bioRxiv - Microbiology 2022Quote: ... cells were resuspended in staining solution containing anti-p24 FITC (Beckman Coulter #6604665; clone KC57) and BD Perm/Wash Buffer for a final staining volume of 50μl ...
-
bioRxiv - Cell Biology 2023Quote: ... in the presence or absence of plate-bound anti-CD3 antibody (clone UCHT1, Beckman Coulter) and soluble anti-CD28 antibody (clone CD28.2 ...
-
bioRxiv - Immunology 2023Quote: ... and the fluorescent anti-p24 mAb (PE-conjugated anti-p24, clone KC57; Beckman Coulter/Immunotech). The percentage of infected cells (p24+ cells ...
-
bioRxiv - Cancer Biology 2021Quote: ... Purified cDNA was amplified for 15 cycles and cleaned up using SPRIselect beads (Beckman). Samples were quantified on an Invitrogen Qubit 4 Fluorometer ...
-
bioRxiv - Genomics 2020Quote: ... Purified cDNA was amplified for 15 cycles before bead cleanup using SPRIselect beads (Beckman). Samples were quantified using an Invitrogen Qubit 4 Fluorometer ...
-
bioRxiv - Pathology 2021Quote: ... the double-stranded cDNA was purified with AMPure XP beads (Beckman Coulter, Inc. CA), and subjected to library preparation using the Nextera XT DNA sample Prep kit (Illumina Inc.) ...
-
bioRxiv - Bioengineering 2020Quote: ... Purified cDNA was PCR amplified and further purified with SPRIselect reagent (Beckman Coulter, B23318). Final libraries were generated after fragmentation ...
-
bioRxiv - Neuroscience 2020Quote: ... All cDNA and library clean-up was done using SPRIselect beads (Beckman Coulter B23317).
-
bioRxiv - Genomics 2022Quote: ... cDNA pool was then treated with RNAseA and purified with AMPure XP beads (Beckman). We conducted junction PCR with the KAPA HiFi HotStart ReadyMix PCR Kit (KK2601 ...
-
bioRxiv - Neuroscience 2021Quote: ... The double-stranded cDNA samples were cleaned up by 1.8x SPRI beads (Beckman Coulter) and treated with Exonuclease I (New England Biolabs ...
-
bioRxiv - Genomics 2020Quote: ... the cDNA was purified using equal volume of Agencout AMPure XP beads (Beckman Coulter). 100 ng or 1 ng purified cDNAs were used for library construction using either TruSeq DNA Nano library preparation kit (Illumina) ...
-
bioRxiv - Microbiology 2021Quote: ... then size selected cDNAs were synthesized with Ampure XP system (Beckman Coulter, Beverly, USA).
-
bioRxiv - Developmental Biology 2021Quote: ... cDNA was purified using a 1:1 volumetric ratio of Ampure Beads (Beckman Coulter) and eluted in 20 ml of water ...
-
bioRxiv - Immunology 2021Quote: ... Amplified cDNA product was cleaned up with the SPRI select Reagent Kit (Beckman Coulter). Indexed sequencing libraries were constructed using the reagents from the Chromium Single Cell 3’ v3 Reagent Kit ...
-
bioRxiv - Genomics 2021Quote: ... The cDNAs and the libraries were washed using AMPure XP beads (Agencourt, Beckman Coulter) after every enzymatic reaction step ...
-
bioRxiv - Immunology 2021Quote: ... The 10 cDNA plates were cleaned-up using AMPure XP beads (Beckman Coulter #A63881), deep 96 well plates (Abgene #AB-0765 ...
-
bioRxiv - Microbiology 2022Quote: ... The amplified cDNA was purified using the Agencourt AMPure XP kit (Beckman Coulter Genomics) and evaluated via capillary electrophoresis ...
-
bioRxiv - Plant Biology 2023Quote: ... The cDNA was purified using an Agencourt AMPure XP kit (Beckman Coulter Genomics, USA). For Illumina NextSeq sequencing ...
-
bioRxiv - Molecular Biology 2024Quote: ... The resulting cDNA libraries were purified with solid-phase reversible immobilization SPRI beads (Beckman) and checked on a BioAnalyzer High sensitivity chip (Agilent ...
-
bioRxiv - Developmental Biology 2024Quote: ... Post cDNA amplification and cleanup was performed using SPRI select reagent (Beckman Coulter B23318). Post cDNA amplification and post-library construction quality control was performed using the Agilent Bioanalyzer High Sensitivity kit (Agilent 5067–4626) ...
-
bioRxiv - Molecular Biology 2024Quote: ... The double-stranded cDNA product was purified with 0.8× AMPure XP beads (Beckman Coulter). The IVT RNA control was prepared by T7 in vitro transcription using the purified cDNA product and HiScribe T7 High Yield RNA Synthesis Kit according to the manufacturer’s protocol ...
-
bioRxiv - Neuroscience 2024Quote: ... The amplified cDNA samples were purified with Ampure XP magnetic beads (Beckman Coulter, CA), quantified by Qubit fluorometer (Invitrogen ...
-
bioRxiv - Immunology 2024Quote: ... The cDNA was cleaned up by a 1.6X AMPure XP bead cleanup (Beckman, #A63881) with a final elution of 23 µl ...
-
bioRxiv - Microbiology 2023Quote: ... Bead cleanup of cDNA was automated using the Biomek NXP liquid handler (Beckman Coulter), AMpure beads and an Alpaqua 384 post magnet with spring cushion technology (Alpaqua) ...
-
bioRxiv - Neuroscience 2024Quote: ... Amplified cDNA was then purified with Agencourt AMPure XP beads (Beckman Coulter, Cat#: A63882). After quantification ...
-
bioRxiv - Plant Biology 2023Quote: ... Double-stranded cDNA was cleaned with AMPure XP Beads (1X) (Beckman Coulter, Brea, California,). The cDNA products were incubated with Klenow DNA Polymerase to add a single “A” nucleotide to the 3’ end of the blunt DNA fragments ...
-
bioRxiv - Cell Biology 2023Quote: ... The cDNA was amplified by PCR and purified with AMPure beads (Beckman Coulter, A63881). The libraries were quantified with a KAPA Library Quantification Kit (KAPA Biosystems ...
-
bioRxiv - Genomics 2023Quote: ... the cDNA was cleaned up and eluted into 15 µL using AMPure beads (Beckman) following the manufacturer’s protocol ...
-
bioRxiv - Microbiology 2023Quote: ... Double-stranded cDNA was cleaned up with AMPure XP Beads (1.8X) (Agencourt, Beckman Coulter). The cDNA products were incubated with Klenow DNA Polymerase to add a single ‘A’ nucleotide to the 3’ end of the blunt DNA fragments ...
-
bioRxiv - Genomics 2023Quote: ... Double-stranded cDNA was purified by paramagnetic beads (Agencourt AMPure XP beads, Beckman Coulter). The cDNA products were incubated with Klenow DNA Polymerase to add an ‘A’ base (Adenine ...
-
bioRxiv - Developmental Biology 2023Quote: ... double-stranded cDNA was purified using Agencourt AMPure XP beads (Beckman Coulter, cat #A63882). Validation PCRs were performed using the primers listed in Supplemental Table T1.