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Biocad sprint

Manufactured by Thermo Fisher Scientific
Sourced in United States

The BioCad Sprint is a high-performance liquid chromatography (HPLC) system designed for fast and efficient biomolecule purification. It features a compact design and advanced software for streamlined operation.

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2 protocols using biocad sprint

1

Solid-Phase Peptide Synthesis and Purification

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Peptides were synthesized using the stepwise solid-phase method by 9-fluorenylmethoxycarbonyl (Fmoc) chemistry on Wang resin (AnaSpec, Fremont, CA, USA) with a 12-channel multiplex peptide synthesizer (Protein Technologies, Tucson, AZ, USA) according to the manufacturer’s procedures. Detachment of peptide from the resin and removal of the side chain protection groups were done by incubating the resin with a mixture of trifloroacetic acid (TFA):Thioanisole:Water:Phenol:1,2-ethanedithio (82.5:5:5:5:2.5 v/v) for 2 hours.
The crude peptide was purified on a preparative Kinetex reversed-phase C18 column, 150 × 21.1 mm (Phenomenex, Torrance, CA, USA) using a BioCad Sprint (Applied Biosystems, Foster City, CA, USA). A flow rate of 30 mL/min with solvent A (0.1% TFA in deionized water) and solvent B (0.1% TFA in acetonitrile) was used. The column is equilibrated with 5% solvent B before sample injection. Elution is performed with a linear gradient from 5% solvent B to 100% solvent B in 60 min. The absorbance of the column effluent is monitored at 214 nm, and peak fractions are pooled and lyophilized.
The pure peptide fraction is identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) or electrospray ionization mass spectrometry (ESI-MS) and lyophilized.
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2

Synthesis and Purification of Histatin-1 Peptide

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Linear histatin-1 peptide was synthesized using the stepwise solid-phase method by the 9-fluorenylmethoxycarbonyl (Fmoc) chemistry on the Wang resin (AnaSpec, Fremont, CA, USA) with a 12 channel multiplex peptide synthesizer (Protein Technologies, Tucson, AZ, USA) according to the manufacturer’s protocol. The crude peptides were then purified on a preparative Kinetex reversed-phase C18 column, 150 x 21.1 mm (Phenomenex, CA, USA) using a BioCad Sprint (Applied Biosystems, CA, USA). The pure peptide fraction were identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) or electrospray ionization mass spectrometry (ESI MS) and lyophilized as appropriate. 1000μM and 500μM stock solution of histatin-1 was made by dissolving lyophilized peptide in phosphate buffer saline (PBS) and utilized in all the studies described below.
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