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5α dht

Manufactured by Merck Group
Sourced in United States, Germany

5α-DHT is a chemical compound used in research laboratories. It is a metabolite of the male hormone testosterone and plays a role in various physiological processes. The primary function of 5α-DHT is to serve as a tool for scientific investigation and experimentation, particularly in the fields of endocrinology and biochemistry.

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5 protocols using 5α dht

1

Experimental Evaluation of Vasoactive Compounds

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The following compounds were obtained from Sigma (St. Louis, MO, U.S.A.): testosterone (TES; 17β-hydroxy-4-andosten-3-one), 5α-DHT (17β-hydroxy-5α- androstan-3-one), acetylcholine chloride (ACh), L-Norepinephrine hydrochloride (NA), sodium nitroprusside (SNP), caltinonin gene related peptide (CGRP). 5β-DHT (17β- hydroxy-5β-androstan-3-one) was obtained from Steraloids (Newport, RI, U.S.A.).
The androgens were prepared separately as a stock solution (0.1 M) in absolute ethanol and then diluted in absolute ethanol to the concentration required for each experiment; final ethanol concentration in the tissue baths never exceeded 0.1% (v/v) of the vehicle. The remaining drugs were dissolved in distilled water except the NA which was dissolved in a NaCl (0.9%)-ascorbic acid (0.01% w/v) solution; appropriate dilutions were prepared in KHS on the day of the experiment. Moreover, SNP was kept in the dark until use to avoid light-induced degradation.
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2

Osteoblastic Cell Line MC3T3-E1 Characterization

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The mouse calvariae origin osteoblastic cell line (MC3T3-E1) subclone 14 (CRL-2594, highly differen-tiating) purchased from American Type Culture Collection (ATCC) Cell Bank (Manassas, VA, USA) was used as in vitro model. Cell culture reagents (alpha modified minimal essential medium (α-MEM), penicillin & streptomycin and fetal bovine serum (FBS)) were sourced from Gibco Laboratories (Grand Island, NY, USA). Ascorbic acid, β-glycerophosphate, and MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxy-methoxyphenyl)-2-(4-sulfophenyl)-2H tetrazolium) dye were purchased from Sigma-Aldrich, USA. ALP activity assay kit was purchased from Abcam (ab83369) (USA). 5α-DHT and crystal violet powder were purchased from Sigma Aldrich, Germany. All other chemicals were sourced from the pharmaco-logy and cell culture laboratories of Universiti Kebangsaan Malaysia (UKM). All reagents and plastic wares used were trace element free and were analyzed for high purity grade.
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3

Enzyme Purification and Analysis Protocol

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The following chemicals were used in the experiments: Na2HPO4, NaH2PO4, NaCl, bovine serum albumin (BSA), imidazole, 5α-DHT, methylglyoxal, 9,10-phenanthrenequinone and hydrindantin were purchased from Sigma (St. Louis, MO), and Ni-NTA chelating agarose CL-6B was purchased from Peptron company (Daejon, Korea). Bradford Protein assay kit and Ultrafree-0.5 Centrifugal Filter Device were purchased from Bio-Rad (Richmond, CA) and Millipore (Bedford, MA), respectively.
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4

Evaluating Molecular Responses to Androgen Receptor Modulators

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5α-DHT, casodex, and Enzalutamide were obtained from Sigma and were resuspended in DMSO (Sigma). Primers were designed manually and were purchased from Integrated DNA Technologies. Anti-ESRP1 (#21045-111-AP) and anti-ESRP2 (#23317-1-AP) were obtained from the Proteintech. E-Cadherin (4A2) (#14472) and Vimentin (D21He) (#5741) were obtained from the CellSignaling, while anti-aTubulin antibody (#A01410) was obtained from Genscript. All other reagents if not specified were obtained from Thermo fisher Scientific.
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5

ILC2 Differentiation Modulated by Androgen

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To induce ILC2 differentiation in vitro, cell-sorted ILC2Ps from female bone marrow cells were cultured for 7 d in α-MEM complete medium (10% heat-inactivated FCS) on OP9-DL1 with 10 ng/ml each of SCF, IL-7, and IL-33. 5-α DHT (Sigma-Aldrich) or the AR antagonist flutamide (Sigma-Aldrich) were diluted in methanol, respectively at 10−2 M and 10−3 M, to generate a stock solution and then added at the indicated concentration on day 0, +4, and +7 of culture.
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