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Ammonium iron 2 sulfate hexahydrate

Manufactured by Fujifilm
Sourced in Japan

Ammonium iron (II) sulfate hexahydrate is a chemical compound commonly used in laboratory settings. It is a crystalline solid with a pale green color. The compound's core function is to serve as a reducing agent and a source of ferrous ions in various analytical and experimental procedures.

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3 protocols using ammonium iron 2 sulfate hexahydrate

1

Epigenetic Modifications Analysis

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Single-stranded M13mp18 viral DNA, T4-βGT (10 units/μl), MspI (20 units/μL) and uridine-diphosphoglucose (UDP-Glc) were purchased from New England Biolabs (Ipswich, MA, USA). TET1 was purchased from Wisegene (Chicago, IL, USA). ARP [aldehyde reactive probe; O-(biotinylcarbazoylmethyl) hydroxylamine] was purchased from Cayman Chemical (Ann Arbor, MI, USA). Recombinant human TDG protein was purchased from Novus Biologicals (Centennial, CO, USA). Real-time PCR mix was purchased from Takara (Kyoto, Japan). All short oligonucleotides including staple DNAs were purchased from Eurofins Genomics (Tokyo Japan). Chemically modified DNA oligonucleotides were obtained from Japan Bioservices (Saitama, Japan). Ammonium iron (II) sulfate hexahydrate, l-ascorbic acid, α-ketoglutarate, dl-dithiothreitol, adenosine triphosphate, 25% glutaraldehyde acid were purchased from Wako pure chemical industries (Kyoto, Japan). 1 M HEPES buffer (pH 7.5), 1 M Tris buffer (pH 7.6) were obtained from Sigma-Aldrich. The buffer 10× NEB 4 [500 mM potassium acetate, 200 mM Tris-acetate, 100 mM magnesium acetate, 10 mM DTT], and 10× cut smart buffer [500 mM potassium acetate, 200 mM Tris-acetate, 100 mM magnesium acetate, 1 mg/ml BSA] were provided by New England Biolabs.
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2

Scalable Recombinant Protein Production

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Cultivation was performed at KNC Laboratories. For preculture, 100 µL of pFusionBM3‐WT/BL21 (DE3) glycerol stock was inoculated in 500 mL of modified LB liquid culture medium (animal‐derived material‐free) containing 25 µg/mL kanamycin sulfate and cultured at 25°C for 22 hours with shaking at 120 rpm.
1 L of precultured liquid was added to 150 L of modified 2 × YT medium (animal‐derived material‐free) containing 25 µg/mL kanamycin sulfate, 80 µg/mL 5‐aminolevulinic acid (Wako), 100 µM ammonium iron (II) sulfate hexahydrate (Wako), 250 µmol/L isopropyl β‐D‐thiogalactopyranoside (IPTG; Wako) and cultured at 20°C for 47 hours with ventilation rate of 75 L/min. 2 × YT medium was comprised of 1.6% (wt/vol) Difco select soytone, 1% (wt/vol) Bacto yeast extract and 0.5% (wt/vol) sodium chloride. pH in culture was maintained at pH 7.0 ± 0.1 using 25% (vol/vol) ammonia solution (Wako) and 2 mol/L phosphoric acid (Wako), and dissolved oxygen was maintained at DO 1.5 ± 0.5 ppm by stirring.
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3

Synthesis and Characterization of IL C4mimTf2N

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The IL C4mimTf2N was synthesized according to a reported procedure. 50, 51 The extraction reagents bpy and TOPO were purchased from FUJIFILM Wako Pure Chemical Corporation (Osaka, Japan) and Dojindo (Kumamoto, Japan), respectively. A stock standard solution of Fe(II) (250 mg dm -3 ) was prepared by dissolving ammonium iron(II) sulfate hexahydrate (FUJIFILM Wako Pure Chemical Corporation, reagent grade) in 0.1 mol dm -3 HNO3. A stock standard solution of Fe(III) (250 mg dm -3 ) was prepared by diluting 1000 mg dm -3 Fe atomic absorption spectrometry standard solution (Fe(NO)3 in 0.275 mol dm -3 HNO3) purchased from Nacalai Tesque (Kyoto, Japan) with 0.1 mol dm -3 HNO3. Other chemicals and solvents included reagent-grade materials, and were used without further purification. High-purity water was produced with a Millipore Direct-Q water purification system.
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