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This medium allows the transformed cells to recover optimally. In the SOC medium, tryptone and yeast extract provide E. coli with a source of carbon and nitrogen, in addition, the medium contains minerals, vitamins and amino acids. Sodium chloride and potassium chloride in the medium maintain ion transport and osmotic balance.
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Super optimal medium with catabolic repressor (SOC) medium is a glucose-rich microbial growth medium used primarily in the recovery step of Escherichia coli competent cell transformations. The culture of E.coli cells in this nutrient-rich microbial broth increases the transformation efficiency of recombinant plasmids containing toxic protein genes by inhibiting the unintended activation of the.
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Soc medium preparation: Used in bacterial transformation. Ingredients for SOB: 0.5% (w/v) yeast extract 2% (w/v) tryptone 10 mM NaCl 2.5 mM KCl 20 mM MgSO 4 Per liter: 5 g yeast extract 20 g tryptone 0.584 g NaCl 0.186 g KCl 2.4 g MgSO 4 Note: Some formulations of SOB use 10 mM MgCl 2 and 10 mM MgSO 4
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Just before use, add 5 mL of a sterile solution of 2 m MgCl 2. (This solution is made by dissolving 19 g of MgCl 2 in 90 mL of deionized H 2 O. Adjust the volume of the solution to 100 mL with deionized H 2 O and sterilize by autoclaving for 20 min at 15 psi [1.05 kg/cm 2] on liquid cycle.) For solid medium, please see the recipe entitled.
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Recipe. SOC Medium for E. coli. Reagent Final concentration; Tryptone: 2% (w/v) Yeast extract: 0.5% (w/v) NaCl: 10 m m: KCl: 2.5 m m: MgCl 2: 10 m m: Glucose: 20 m m: Prepare a solution containing the first four reagents, sterilize at 121 °C, and then add sterile MgCl 2 and glucose.
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Step 3: Cool down the medium to room temperature. Add 2.5 ml of 1M KCl and mix. Adjust the pH 7.0 with 5N NaOH (~0.2 ml). Note:The SOB medium is not very highly buffered. The pH of the medium drops, as the growing culture reaches the near saturation phase. Step 4: Adjust the volume to 960 ml with deionized / Milli-Q water.
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SOC Medium, shorthand for Super Optimal broth with Catabolite repression, is a nutritionally rich bacterial culture medium. The recipe is differs slightly with LB broth, containing 20 g/L tryptone, 5 g/L yeast extract, and 0.5 g/L sodium chloride. A defining ingredient is 20 mM glucose, which must be added separately after the media has cooled.
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SOC Broth is a rich media used primarily in the recovery step of Escherichia coli competent cell transformations. Use of SOC Broth maximizes the transformation efficiency of competent cells. Directions per Liter: Dissolve 34.46g in 800-900ml of ddH2O stirring gently with heating until completely solubilized. Adjust pH of the medium to the.
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Making SOB into SOC: Per 1L of SOB, add 20mL of filter-sterilized 20% glucose solution. CRITICAL Do this under the flow hood. Make sure SOB medium is cooled to <50 C before adding glucose if it is fresh out of the autoclave. If using 50% glucose solution, add 8mL per 1L SOB. We commonly work with 50mL aliquots of SOB and have a 50% stock.
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2.5 mM KCl. 10 mM MgCl2. 10 mM MgSO4. 20 mM Glucose*. *Note: add Glucose after autoclaving the solution with the remaining ingredients, and letting it cool down. Sterilize the final solution by passing it through a 0.2 µm filter. SOC medium can be stored at room temperature and is stable for several years. icon_0011_idea-s.
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S.O.C. medium has the same formulation as the rich S.O.B. (Super Optimal Broth) medium with additionally added 10 mM MgCl 2 and 20 mM glucose (as published by Hanahan in 1983). S.O.C. Medium is supplied as 10 x 10 mL bottles of ready-to-use liquid medium. Each lot of S.O.C. Medium is tested to ensure conformance with the most current approved.
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Super Optimal Broth (SOB medium) is a nutrient-rich bacterial growth medium used for microbiological culture, generally of Escherichia coli.This nutrient-rich microbial broth contains peptides, amino acids, water soluble vitamins and glucose in a low-salt formulation. It was developed by Douglas Hanahan in 1983 and is an adjusted version of the commonly used LB medium (lysogeny broth).
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SOB. For solid medium, please see Media Containing Agar or Agarose. Shake until the solutes have dissolved. Add 10 ml of a 250 mM solution of KCl. (This solution is made by dissolving 1.86 g of KCl in 100 ml of deionized H 2 O.) Adjust the pH of the medium to 7.0 with 5 N NaOH (approx. 0.2 ml). Adjust the volume of the solution to 1 liter with.
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Add SOC to freshly transformed E. coli cells and incubate for up to 1 hour before plating on selective media. 1X SOC Outgrowth Medium: 2% Vegetable Peptone 0.5% Yeast Extract 10 mM NaCl 2.5 mM KCl 10 mM MgCl2 10 mM MgSO4 20 mM Glucose. This product is related to the following categories: Competent Cells Buffers & Diluents Products, Buffers Products
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The following recipe is standardized to 1 L 1. Prepare stock solutions of glucose, MgCl2 and MgSO4 and filter sterilize them a. Glucose 2 M: 18 g glucose in 90 mL of ddH2O, fill up to 100 mL b. MgCl2 2 M: 19 g MgCl2 in 90 mL of ddH2O, fill up to 100 mL c. MgSO4 2 M: 49.3 g MgSO4 x 7 H2O in 90 mL of ddH2O, fill up to 100 mL d.
