Selection on sand in a plastic-petri plate started with saturating chromatography sand with liquid MS0 media (1.1 g/L MS basal salt, 0.5 g/L MES; adjusted pH 5.7). The sands reported here were i) Silicon dioxide (SiO2); purum p.a.; acid purified; 40–200 mesh (84880 – Fluka), and ii) Quartz (SiO2); purum p.a.; powder; < 230 mesh (00653 – Sigma). Appropriate antibiotics were added to the MS0 solution before sand saturation. Dry seeds were sprinkled onto the wet sand, and after a two-day treatment at 4°C, plants were allowed to grow for two weeks.
Sterilization
It is a critical step in various fields, such as healthcare, food processing, and scientific research, to prevent the spread of infectious agents and ensure the safety and effectiveness of medical procedures, products, and experiments.
The PubCompare.ai platform leverages advanced AI technollogy to help researchers and professionals optimize their sterilization protocols by identifying the most effective methods from literature, pre-prints, and patents.
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Selection on sand in a plastic-petri plate started with saturating chromatography sand with liquid MS0 media (1.1 g/L MS basal salt, 0.5 g/L MES; adjusted pH 5.7). The sands reported here were i) Silicon dioxide (SiO2); purum p.a.; acid purified; 40–200 mesh (84880 – Fluka), and ii) Quartz (SiO2); purum p.a.; powder; < 230 mesh (00653 – Sigma). Appropriate antibiotics were added to the MS0 solution before sand saturation. Dry seeds were sprinkled onto the wet sand, and after a two-day treatment at 4°C, plants were allowed to grow for two weeks.
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Most recents protocols related to «Sterilization»
EXAMPLE 36
Peripheral blood mononuclear cells were prepared from blood samples obtained from llama No. 45 and No. 46 using Ficoll-Hypaque according to the manufacturer's instructions. Next, total RNA extracted was extracted from these cells and used as starting material for RT-PCR to amplify Nanobody encoding gene fragments. These fragments were cloned into phagemid vector pAX50. Phage was prepared according to standard methods (see for example the prior art and applications filed by applicant cited herein) and stored after filter sterilization at 4° C. for further use.
Example 3
Astragalus membranaceus was crushed and sieved through 8 mesh to obtain Astragalus membranaceus powder. The Astragalus membranaceus powder was mixed evenly with distilled water with a weight ratio of 2.5:1, sterilized in a steam sterilization pot at 90° C. for 60 min, and then cooled to room temperature to obtain a solid medium of Astragalus membranaceus. Paecilomyces cicadae was evenly inoculated into the solid medium of Astragalus membranaceus with an inoculation amount of 20 wt % of Astragalus membranaceus. The inoculated medium was cultured at a constant temperature of 26° C. and a constant relative humidity of 80% for 24 days to obtain fermentation fungal substance of Astragalus membranaceus/Paecilomyces cicadae E (hereinafter referred to as “fungal substance E”).
Example 2
This example illustrates the heavy metal acceptability of B. licheniformis strain ECOBIO_2.
The pure cultures of each isolates were grown in LB broth and the bacterial cell concentration was spectrophotometrically adjusted to have an OD of 1.0 at A600 nm. 1 ml of cells were inoculated to 100 ml of sterilize LB medium amended with either 1 mM Pb(C2H3O2)2, CdCl2, K2Cr2O7 or with 0.3 mM HgCl2 in individual culture flasks. Flasks were incubated at 37° C. and 150 rpm. The growth rate was measured by assessing the turbidity of the medium every 24 hours after initial incubation for 3 days.
Data obtained from three independent experiments performed to determine the heavy metal acceptability of strain ECOBIO_2. Results (shown in
Example 2
BC non-woven was produced by the method of the present invention. In particular, BC non-woven was sterilized with e-beam or by exposure to steam after removal from the culture vessel and separation from the BC that remained in the culture vessel. The BC network structure was investigated with scanning electron microscopy. It was found that the network structure was neither disturbed by sterilization with steam nor by e-beam sterilization.
EXAMPLE 12
Peripheral blood mononuclear cells were prepared from blood samples obtained from llama No. 146 and No. 147 using Ficoll-Hypaque according to the manufacturer's instructions. Next, total RNA extracted was extracted from these cells and used as starting material for RT-PCR to amplify Nanobody encoding gene fragments. These fragments were cloned into phagemid vector pAX50. Phage was prepared according to standard methods (see for example the prior art and applications filed by applicant cited herein) and stored after filter sterilization at 4° C. for further use.
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More about "Sterilization"
This essential step ensures the safety and efficacy of medical procedures, scientific experiments, and food production.
The PubCompare.ai platform leverages advanced AI technology to help researchers and professionals optimize their sterilization protocols, enabling them to identify the most effective methods from the vast body of literature, pre-prints, and patents.
Researchers and professionals working in healthcare, food processing, and scientific research can benefit from the seamless comparison tools offered by PubCompare.ai.
The platform allows users to compare various sterilization techniques and products, helping them streamline their processes and elevate the quality of their research.
By identifying the most effective sterilization protocols, users can ensure reproducible and accurate results, crucial for the success of their work.
In addition to sterilization, other key laboratory techniques and materials play a vital role in various fields.
Fetal Bovine Serum (FBS), a commonly used cell culture supplement, provides essential nutrients for cell growth and proliferation.
Dulbecco's Modified Eagle Medium (DMEM) is a widely used cell culture medium that supports the growth and maintenance of a variety of cell types.
Penicillin and streptomycin, antibiotics, are often added to cell culture media to prevent bacterial contamination.
Phosphate-Buffered Saline (PBS) is a versatile buffer solution used in numerous biological applications, while Sylgard 184 is a silicone elastomer commonly used for microfluidic device fabrication.
By leveraging the insights from these related terms, researchers can further enhance their experimental protocols and ensure the reliability of their findings.