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Naocl

Manufactured by Carl Roth
Sourced in Germany

NaOCl is a chemical compound composed of sodium, oxygen, and chlorine. It is commonly known as sodium hypochlorite and is a powerful oxidizing agent. NaOCl is a clear, yellowish-green liquid with a distinctive chlorine-like odor. It is widely used as a disinfectant, bleaching agent, and oxidizing agent in various industrial and laboratory applications.

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2 protocols using naocl

1

Polyether Sulfone Ultrafiltration Membrane Fabrication

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The polyether sulfone (PES) ultrafiltration membrane modules, comprising 10 Multibore® fibers, each containing 7 capillaries with an inner diameter of 0.9 mm, were supplied by inge GmbH (DuPont, Greifenberg, Germany). Each membrane module has an overall membrane surface of 0.05 m2 and molecular weight cut-off (MWCO) of 100 kDa. Polydiallyldimethylammonium chloride (PDADMAC) (20% solution with a molecular weight of 250–350 kDa) and poly-(4-styrenesulfonic acid) (PSS) (molecular weight of 1000 kDa) were purchased from Sigma Aldrich (Schnelldorf, Germany). NaCl, MgSO4, CaCl2 and NaOCl were purchased from Carl Roth GmbH (Karlsruhe, Germany). All salts were of analytical grade.
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2

Rucola Seedlings Inoculation with Rhodococcus Strains

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Rucola (Eruca sativa L.) seeds were washed in Tween 80 1% (Sigma, United States) for 2 min, surface sterilized with sodium hypochlorite 12% (NaOCl, Roth, Germany) for 8 min and washed three times in sterile deionized water for 2 min. Sterilized seeds were placed on Hoagland’s solution (Sigma, United States) with 0.8% agar to germinate 4 days. Rhodococcus strains were pre-grown in TSB. Overnight grown cultures were washed two times in 1x PBS (AppliChem, Germany) and diluted to a concentration of 107 CFUs. Seedlings were inoculated in the prepared bacterial solution of RL1, BG43, and djl6 for 1 h under shaking at 160 rpm at 28°C. Seedlings inoculated in 1x PBS served as negative control. Inoculated seedlings were transferred to an axenic system with 80 ml sterile quartz sand and 20 ml Hoagland’s solution in a sterile Phytatray II (Sigma, United States). Seedlings inoculated with RL1 were additionally transferred on plates with 0.5x Murashige and Skoog Medium (0.5x MS) including vitamins (Duchefa Biochemie, Netherlands); pH was adjusted to 5.7 with 2N KOH. No additional sucrose was added to 0.5x MS. The axenic system was placed in a Phytochamber (Weiss Technik, Modell SGC120PG2, Germany) with 23°C, 55% humidity, day-night-cycle 12 h : 12 h. After seven and 14 days freshly harvested roots were washed in 1x PBS, fixed in 55% EtOH and 1x PBS mix and stored at –20°C until further use.
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