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N phosphonomethyl glycine

Manufactured by Merck Group
Sourced in United States

N-(phosphonomethyl)glycine is a compound used as a laboratory reagent. It is a colorless, odorless crystalline solid. The compound is used in various analytical and research applications, but no further details on its specific functions can be provided without the risk of extrapolation.

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Lab products found in correlation

3 protocols using n phosphonomethyl glycine

1

Evaluating Glyphosate and Folate Impact on Tsetse Lipid Metabolism

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Groups of G. morsitans flies were maintained on a diet containing 100 μM glyphosate combined with 500 nM folic acid [N-(phosphonomethyl)glycine; Sigma-Aldrich, St. Louis, MO, USA] or (Sigma-Aldrich). This treatment has been previously shown to impact folate synthesis.28 (link),35 (link) Following six bloodmeals, the flies were examined to determine if lipid and phosphatidylcholine levels were increased or decreased. These treatments were conducted to eliminate potential off-target effects of tetracycline supplementation to validate Wigglesworthia’s role in tsetse lipid metabolism, and to provide a secondary validation of impaired lipid metabolism without treatment with antibiotics.
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2

Glyphosate Exposure Regime for Plants

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Plants were grown in the greenhouse under natural light conditions. A 200 μm glyphosate solution (N-phosphonomethyl glycine (Sigma Aldrich) in 10 mm (NH4)2SO4 and 0.01% w/v Tween-20) was applied to 20-day-old soil grown plants at 5:00, 9:00, 13:00, 17:00 and 21:00 h by using a herbicide spray booth ‘Generation III’, (De Vries, Hollandale, MN, USA). The sprayed 200 μm glyphosate solution resulted in an application of 0.2535 mg m−2 as determined by spray speed, length and spray volume under 240 kpa pressure. The control spray contained 10 mm (NH4)2SO4 and 0.01% w/v Tween-20.
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3

Micropropagation and Rooting of TME 204

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Approximately 1.0‐ to 1.5‐cm‐long shoots were excised from 6‐week‐old micropropagated mother plants of TME 204 (Chauhan et al., 2015), events obtained from H001, H002, H003, H004, H080 and H081, and subcultured onto MS medium supplemented with 2% w/v sucrose solidified with 0.22% w/v phytagel. Filter‐sterilized glyphosate [N‐(phosphonomethyl) glycine, Sigma‐Aldrich] at 0.05 mm was added after autoclaving. Cultures were incubated under 16‐h photoperiod (75 μmol m−2s−1 irradiance) at 28 ± 1 °C. Root formation was assessed per shoot explant every week for 3 weeks.
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