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Murashige and skoog basal salts

Manufactured by Caisson
Sourced in United States

Murashige and Skoog basal salts are a formulation of inorganic salts commonly used as a base medium for plant tissue culture and micropropagation. The salts provide essential nutrients for the growth and development of plant cells, tissues, and organs in an in vitro environment. The composition of the salts is designed to support the specific nutritional requirements of a wide range of plant species.

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3 protocols using murashige and skoog basal salts

1

Grand Nain Banana Tissue Culture

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Grand Nain banana tissue culture plants (kindly provided by Miguel Muñoz, Dole Food Company) were maintained on modified Murashige and Skoog medium [76 (link)]. Growth medium was prepared with 4.33 g/L Murashige and Skoog basal salts (Caisson labs), 30g/L sucrose, 200 ug/L glycine, 50 ug/L niacin, 50 ug/L pyridoxine, 10 ug/L thiamin, 10 ug/L myo-inositol, 1 ug/L cysteine, 2 g/L Phytagel (Sigma-Aldrich), with or without 4.5 mg/L 6-benzylaminopurine (BAP), with the pH adjusted to 5.8. Medium with BAP is used for bud proliferation, while medium without BAP is used for rooting. Plants were maintained on an 18h light/6h dark photoperiod with cool white fluorescent light at 25–30°C.
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2

Arabidopsis thaliana Seedling Growth Protocol

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Arabidopsis thaliana ecotype Col-0 was used as wild type (WT). The koin-1 (WiscDsLox_439H07) and koin-2 (Gabi-Kat822B12) alleles were obtained from the ABRC (Arabidopsis Resource Center). The genotypes IRKp:IRK:GFP, SCRp:IRK-GFP, CO2p:IRK-GFP, pub4-1 SCRp:IRK:GFP, irk-4, irk-1, SCRp:IRK:GFP irk-4, IRKp:IRK:GFP irk-4, pSCR:erGFP, scr-4 were previously described15 (link). Unless otherwise specified, seeds were surface sterilized by chlorine gas, sown on solid Arabidopsis medium 1X Murashige and Skoog basal salts (Caisson labs), 0.5 g/L MES, 1% sucrose, and 1% agar (Difco), at pH 5.7; then stratified at 4 °C for at least 2 days prior to transfer to a 16/8 h illumination regime in a Percival growth chamber at a continuous temperature of 22 °C. Seedlings were grown on vertically oriented plates sealed with parafilm or micropore tape for 4–7 days prior to analysis.
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3

Sterilized Tomato Seed Cultivation

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Cultivated tomato S. lycopersicum cv. M82 seeds were obtained from the C.M. Rick Tomato Genetic Resource Center (https://tgrc.ucdavis.edu/; RRID:SCR_014954). Unless otherwise noted, plants were grown under sterile conditions. Tomato seeds were surface sterilized in 40% bleach for 20 min with gentle rocking, rinsed five times with sterile water, and then sown in a straight line on Falcon 150 mm–by–25 mm cell culture dishes (Corning Inc., Corning, NY, USA) containing half-strength Murashige and Skoog basal salts (Caisson Labs, Smithfield, UT, USA), supplemented with Gamborg’s B-5 vitamins (Caisson Labs, Smithfield, UT, USA), 3% sucrose (Thermo Fisher Scientific Inc., Waltham, MA, USA), and 0.7% Phytoblend agar (Caisson Labs, Smithfield, UT, USA) adjusted to pH 5.8. The plates were wrapped in Micropore surgical tape (3M Company Inc., Maplewood, MN, USA), then oriented vertically in steel alloy 4.25″ by 4.5″ by 13.5″ plate racks (Spectrum Diversified Designs LLC, Solon, OH, USA), and stratified in the dark at 25°C for 5 to 7 days to germinate seeds. Thereafter, vertically oriented plates were transferred to a growth chamber and grown under a 12-hour diurnal cycle, 25°C/18°C, 175 μE light intensity.
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