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Citations for 3M :
101 - 120 of 120 citations for Natural Cytotoxicity Triggering Receptor 1 NCR1 Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Bioengineering 2023Quote: ... Hydrogel vaccines received two (double) doses of antigen and a dose adjuvant (20 μg of Pam3CSK4, CpG1826, cGAMP, or 1 μg of 3M-052). For soluble groups ...
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bioRxiv - Biochemistry 2023Quote: ... Hydrophobic modification of the channels surface was achieved by injecting a solution of 1% (v/v) trichloro (1H,1H,2H,2H-perfluorooctyl) silane in HFE-7500 oil (3M Novec) into the channels ...
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bioRxiv - Bioengineering 2023Quote: ... Devices were treated with (tridecafluoro-1,1,2,2-tetrahydrooctyl) trichlorosilane (1% v/v) (Gelest) in fluorinated oil HFE 7500 (3M, Saint Paul, MN, USA) and left for solvent evaporation at 55 °C.
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bioRxiv - Biochemistry 2023Quote: ... the freshly baked microfluidic chips were flushed with 1% (v/v) trichloro (1H, 1H, 2H, 2H)perfluoroacetylsilane in HFE-7500 (3M-Novec). The chips were heated for 10 minutes at 75°C before storage at room temperature ...
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bioRxiv - Molecular Biology 2021Quote: ... Nuclei were lysed by adding one volume of ice-cold Lysis Buffer B (10 mM HEPES pH 7.6, 1mM DTT, 7.5 mM MgCl2, 0.2 mM EDTA, 0.3M NaCl, 1M urea, 1% NP-40) and kept on ice for 10 minutes ...
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bioRxiv - Bioengineering 2021Quote: ... resin composite layers were built up in 1-mm-thick increments to 3 mm thickness (Z250, 3M ESPE, St. Paul, MN, USA). After being stored in deionized water at 37°C for 24 h ...
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bioRxiv - Cancer Biology 2020Quote: ... of cold nuclei lysis buffer (10mM HEPES, pH 7.6, 1mM DTT, 7.5mM MgCl2, 0.2mM EDTA, 0.3M NaCl, 1M Urea, 1% NP-40) was added ...
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bioRxiv - Genomics 2019Quote: ... Slides were washed three times with PBS and incubated with blocking solution (1% Bovine serum albumin, 10% Donkey serum, 0.3M Glycine, 0.1% PBS Tween) for 1 hour at room temperature followed by primary antibody in blocking solution overnight at 4 degrees (see Table 1 for source ...
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bioRxiv - Developmental Biology 2020Quote: ... peptides were desalted with C18 columns and reconstituted in 1% formic acid in water and further separated into five fractions by strong cation exchange chromatography (SCX, 3M Purification, Meriden, CT). Eluates were first dried in a SpeedVac ...
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bioRxiv - Biochemistry 2020Quote: ... The exchange was quenched for 2 min at 1°C with an equal volume of quench buffer (3M guanidine HCl, 0.1% formic acid). Proteins were cleaved with pepsin and separated by reverse-phase chromatography ...
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bioRxiv - Microbiology 2024Quote: ... Thirty dentin slabs of 4 x 4 x 1 mm were obtained and polished with 500 and 1,200 grit sandpaper and finished using Soflex polishing discs (3M, St. Paul, MN, USA). To obtain an initial value for Knoop surface microhardness (SHi) ...
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bioRxiv - Genomics 2020Quote: ... The reaction mixture was loaded immediately into a 1 ml syringe backfilled with HFE-7500 fluorinated oil (3M, catalog no. 98-0212-2928-5) and injected into a flow-focus droplet maker (Supplementary Fig.7a ...
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bioRxiv - Molecular Biology 2021Quote: ... the beads are collected from the final wash and resuspended in 500ul of RNA Extraction Buffer (0.3M NaOAc pH 5.3, 1mM EDTA, 1% SDS), 100ul acid phenol ...
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bioRxiv - Microbiology 2020Quote: ... Alkaline lysis was performed by adding 200 μl solution II (200 mM NaOH; 1% SDS) followed by 150 μl solution III (3M potassium acetate, pH 5.5). The supernatant was extracted in 400 μl phenol:chloroform:isoamyl alcohol and the upper phase mixed with 600 μl 2-propanol and incubated on ice for precipitation of the DNA ...
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bioRxiv - Developmental Biology 2021Quote: ... 2007b) were blocked for one hour with 1% BSA (in PBT: 3mM NaH2PO4·H2O, 7mM Na2PO4, 1.3M NaCl, 0.1% Triton X-100, pH 7.0). Next ...
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bioRxiv - Developmental Biology 2022Quote: ... An additional 200 μl of cold nuclei lysis buffer (20 mM HEPES pH 7.6, 7.5 mM MgCl2, 0.2 mM EDTA, 0.3M NaCl, 1M urea, 1% NP-40, 1mM DTT) was added to the samples ...
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bioRxiv - Cell Biology 2023Quote: ... The pellet containing Golgi membrane was resuspended using 1 ml of washing buffer (25 mM HEPES-KOH pH 7.4, 3M KCl, 2.5 mM Mg(OAc)2 ...
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bioRxiv - Genomics 2020Quote: ... Amplification products were purified using a standard protocol for DNA precipitation with sodium acetate and ethanol (1/10 3M sodium acetate, 2 v/v ethanol) (https://www.thermofisher.com/es/es/home/references/protocols/nucleic-acid-purification-and-analysis/dna-protocol/sodium-acetate-precipitation-of-small-nucleic-acids.html#comergent_product_list_15878) ...
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bioRxiv - Molecular Biology 2022Quote: ... Samples were fixed with ice cold methanol for 5 min and then in blocking buffer (1% BSA, 10 % Horse serum, 0.3M Glycine, 0.2% Triton X in PBS) for 1 h RT ...
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bioRxiv - Cell Biology 2023Quote: ... exchanged into a 1:1 volume mixture of 1X PBST and smiFISH Wash Buffer [10% 20X SSC (20X SSC: 0.3M sodium citrate, 3M NaCl, in nuclease-free H2O, pH7.0), 10% deionized formamide ...