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Falcon 15 ml conical centrifuge tubes

Manufactured by BD
Sourced in Germany

The Falcon™ 15 mL conical centrifuge tubes are laboratory equipment used for sample preparation and processing. They provide a standardized container for the centrifugation of liquid samples up to 15 mL in volume.

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4 protocols using falcon 15 ml conical centrifuge tubes

1

Yeast Growth and Stress Assays

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Yeast cells were grown overnight at 30 °C under constant shaking at 160 rpm in YPD-Zeo medium. For the spotting assays, cultures were then diluted to an OD600 of 1. The resulting cultures were further diluted (1, 0.5, 0.1, 0.05 fold), spotted onto YPD-Zeo plates and incubated for 3 days at 30 °C or 37 °C. For the heat shock assay, cultures at OD600 of 1 were pre-treated for 30 min at 48 °C. Then, they were diluted and spotted as above, and incubated for 3 days at 30 °C. To trace growth profiles in liquid medium, cultures were diluted to an OD600 of 0.1 in YPD-Zeo medium, then incubated at 30 °C or 37 °C under constant shaking at 160 rpm. Growth under limited anaerobic conditions was performed at both 30 °C and 37 °C under shaking at 160 rpm in sealed Falcon™ 15-ml conical centrifuge tubes, each containing 14 ml of growth medium. Growth rates were measured by monitoring the OD600 at different times.
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2

Creaming Index Determination for Emulsions

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In this case, the freshly made coarse emulsion and nanoemulsion were added to Falcon™ 15 mL conical centrifuge tubes (diameter =1.5 cm) and centrifuged at 3000 rpm (150 RFC) for 4 h in a centrifuge (Rotofix 32A, Hetttich GmBH, Tuttlingen, Germany). The value of the creaming index (CI) was determined as
CI=HSHE×100
where HS is the sediment height and HE is the sample height before centrifugation.
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3

Droplet Digital PCR for HPV Detection

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Droplet digital PCR reagents (2x ddPCR™ Supermix for Probes (No dUTP) Catalog # 186–3024; Pipet tips Catalog # 186–4121; Cartridge Catalog # 186–4109 and Sealing foil Catalog #181–4040) were purchased from Bio-Rad (Hercules, CA). Eppendorf™ 96-Well twin.tec™ PCR Plates (Catalog #E951020362), Falcon® 15ml Conical Centrifuge Tubes (Catalog # 352096), Falcon™ 50mL Conical Centrifuge Tubes (Corning #352098), Qubit™ dsDNA HS Assay Kit (Catalog # Q32851), and Qubit™ Assay Tubes (Catalog # Q32856) were purchased from Fisher scientific (Fair Hampton, NH). Bovine Serum Albumin was from Sigma (Catalog # A7906; Sigma–Aldrich, St. Louis, MO). Circulating DNA was quantified with Qubit (Invitrogen, Carlsbad, CA, USA). Target gene fragments for HPV subtype 16, 18, 31, 33, and 35 were synthesized as gBlocks from IDT for use as positive controls (Supplementary Table S1). These gBlocks were cloned into a pCR2.1-TOPO TA vector by Topo TA cloning kit (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s protocol. The gene fragment constructs were verified by Sanger sequencing (Genewiz, New Jersey, USA). FAM-, TET- or HEX-conjugated Locked Nucleic Acids (LNA)-modified DNA oligonucleotide probes and FAM-ZEN dual quencher probes were synthesized by IDT (Integrated DNA Technology, San Jose, CA, see Supplementary Table S1).
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4

Synthesis of Porous Hollow Silica/Organosilica Particles

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To selectively remove the inner core and leave the porous shell relatively intact, Na2CO3 was selected as the etching agent. The synthesized core-shell silica and organosilica particles (csSPs and csOPs, respectively) were resuspended in 12.5 mL of 0.6 M Na2CO3 solution and stirred (500 rpm) at 80 °C for 1 h. The resulting particles were collected by centrifugation (10 min at 5000× g at room temperature in Falcon™ 15 mL conical centrifuge tubes), washed with MQ water two times and then repeated two times with ethanol. Finally, the synthesized hollow particles were resuspended in 10 mL of ethanol solution containing 10% concentrated HCl and stirred at 60 °C for 3 h to remove CTAB. The last step was repeated three times to ensure complete removal of the CTAB. The final products were resuspended in 20 mL MQ water. Different particles are named as porous hollow silica particle-160/280_xyz (pHSP-160/280-xyz) and as porous hollow organosilica particle-160/280-xyz (pHOP-160/280-xyz) based on the type of the used precursor, where the first three digits refer to the nominal diameter of the sSiO2 core (i.e., 160 nm or 280 nm), while x, y, and z refer to the amount of precursor (TEOS or BTEE), ammonia, and surfactant (CTAB), as shown in Table 1.
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