Sodium dodecyl sulfate (sds)

Manufactured by Mallinckrodt

Sodium dodecyl sulfate (SDS) is a commonly used anionic detergent in laboratory settings. Its primary function is to denature proteins by disrupting their non-covalent interactions, thereby allowing for their separation and analysis. SDS is a key component in various biochemical techniques, such as gel electrophoresis and Western blotting.

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Lab products found in correlation

Tris base, by Merck Group (1 mentions) Dsrna ladder, by New England Biolabs (1 mentions) Rnase if, by New England Biolabs (1 mentions) Lysozyme, by Merck Group (1 mentions) 2 log dna ladder, by New England Biolabs (1 mentions) Rnase a, by Thermo Fisher Scientific (1 mentions) Boric acid, by Avantor (1 mentions) Sodium hydroxide (naoh), by Mallinckrodt (1 mentions) Anhydrous ethanol, by Merck Group (1 mentions) Hydroxylamine hydrochloride, by Merck Group (1 mentions) Ammonia borane, by Merck Group (1 mentions)

2 protocols using sodium dodecyl sulfate (sds)

RNA Extraction and Purification Protocol

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Tris base, ethylenediaminetetraacetic acid (EDTA), potassium acetate (KoAc), sodium acetate (NaOAc) and lysozyme were purchased from Sigma-Aldrich. TAE running buffer (50×) was purchased from Omega Bio-Tek. Sodium hydroxide (NaOH) was obtained from EM Science. Boric acid was purchased from JT Baker. Sodium dodecyl sulfate (SDS) was purchased from Mallinckrodt Baker. RNase A/T1 Cocktail Mix and RNase V1 were purchased from Invitrogen/Life Technologies. RNase I_f, 2-log DNA ladder, and dsRNA ladder were purchased from New England Biolabs. RNase A was obtained from Thermo Scientific.

Rodriguez B.V., Malczewskyj E.T., Cabiya J.M., Lewis L.K, & Maeder C. (2015). Identification of RNase-resistant RNAs in Saccharomyces cerevisiae extracts: separation from chromosomal DNA by selective precipitation. Analytical biochemistry, 492, 69-75.

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Synthesis and Semihydrogenation of Alkynes

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Anhydrous copper(ii) chloride (CuCl₂; 97%) and hydroxylamine hydrochloride (NH₂OH·HCl; 99%) were purchased from Aldrich. Sodium hydroxide (98.2%) and sodium dodecyl sulfate (SDS; 100%) were acquired from Mallinckrodt. Diphenylacetylene (DPA; 98%), ammonia borane (H₃N–BH₃; 97%), anhydrous ethanol (99.5%), ethanol-d (C₂H₅OD; 99 atom% D), Cu₂O (99.99%), and Lindlar catalyst (5% palladium deposited on calcium carbonate poisoned with lead) were purchased from Aldrich. All chemicals were used as received without further purification. Ultrapure distilled and deionized water (18.3 MΩ) was used for all solution preparations. Commercially available reagents were used for the semihydrogenation reactions.

Rej S., Madasu M., Tan C.S., Hsia C.F, & Huang M.H. (2018). Polyhedral Cu2O to Cu pseudomorphic conversion for stereoselective alkyne semihydrogenation †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc05232d. Chemical Science, 9(9), 2517-2524.

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