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Chromatography grade ethanol

Manufactured by Merck Group
Sourced in Australia, Germany

Chromatography grade ethanol is a highly purified and filtered ethanol product designed for use in analytical and laboratory applications. It is a clear, colorless liquid with a characteristic odor. The product is suitable for a variety of chromatographic techniques, such as gas chromatography and high-performance liquid chromatography, where high purity and consistency are essential. Chromatography grade ethanol meets the stringent quality and safety standards required for use in sensitive analytical procedures.

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2 protocols using chromatography grade ethanol

1

Differentiation of 3T3-L1 Adipocytes

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For the differentiation of 3T3-L1 cells, stock solutions of differentiation reagents were prepared. Insulin (Sigma-Aldrich, Sydney, Australia) was prepared as a 2 mg/mL solution in 0.01 M aqueous hydrochloric acid (AJAX, Themo Fisher Scientific, Melbourne, Australia) and syringe-filtered. Dexamethasone (Sigma-Aldrich, Sydney, Australia) was prepared as a freezer stock solution of 10 mM stock solution in chromatography grade ethanol (Merck Pty Ltd., Melbourne, Australia), and was further diluted to a working stock solution of 1 mM in phosphate buffered saline, pH 7.4 (PBS; Thermo Fisher Scientific, Melbourne, Australia). 3-Iso-butyl-1-methylxanthine (IBMX; Sigma-Aldrich) was prepared as a 50 mM stock solution in dimethyl sulfoxide (DMSO; Sigma-Aldrich).
Ammonium acetate solution (0.1 M) was prepared via the dissolution of Ammonium acetate (Merck Pty Ltd., Melbourne, Australia) in Milli-Q® ultrapure deionised water (Merck Millipore, Melbourne, Australia). The solution was syringe-filtered prior to use.
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2

Multimodal Identification of Coagulase-Negative Staphylococci

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Following genus-specific identification, CNS were identified to the species level using a combination of methods. All test isolates were amplified using 1 of 2 multiplex PCR assays (multiplex 2 and 3) based on the origin of the isolates. Reactions were prepared in 25-μL volumes using the Qiagen Multiplex PCR kit and amplified according to the manufacturer's instructions. The PCR products were analyzed as described above with the exception that a 1.8% agarose gel (SeaKem, Lonza) was used to resolve the PCR amplicons.
With the exception of one bovine CNS isolate that failed to grow, overnight cultures of all isolates were preserved in chromatography-grade ethanol (Merck) and submitted for MALDI-TOF MS analysis (Bruker Daltonics GmbH, Bremen, Germany). Coagulase-negative staphylococcal isolates that could not be identified using the multiplex-PCR assay or MALDI-TOF MS or where discordant species identifications were obtained using the 2 methods were analyzed further using tuf gene sequencing. The tuf gene was amplified according to the method described by Heikens and coworkers (2005) , and PCR amplicons were submitted to Inqaba Biotechnical Industries (Pretoria, South Africa) for sequencing. Consensus sequences were analyzed in Gen-Bank and cut-off values for the percentage of identity were adjusted to ≥97% sequence similarity.
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