What is the most efficient method to check the compatibility (synergism or antagonism), of a microbial consortium; either of bacteria+bacteria, fungi+fungi or bacteria+fungi.
For fractionation of the lignocellulosic biomass, I need to perform quantification of the cellulose and hemicellulose content. For this purpose, I have performed acid digestion of the sample (72%...
08 September 2018 5,723 0 View
Dear Dr. Cai, my name is Simone Prospero and I work in the team of Phytopathology at the Swiss Federal Institute for Forest Snow and Landscape Research (WSL;...
01 March 2021 1,133 1 View
Incompletely cross-linked pdms are difficult to remove.
01 March 2021 798 3 View
Is the period to autoclave not enough? The inoculation in a hood and flame and UV and alcohol.
27 February 2021 9,356 3 View
What is the most suitable medium of ascomycetes fungi ??
26 February 2021 4,413 1 View
Hi everyone, Illumina provides a list of primers to amplify with high taxonomic coverage the ITS1 region for further fungal sequencing, but I cannot find the exact amount necessary of each...
25 February 2021 6,969 3 View
I am preparing to do a gene knockout in the filamentous fungi Coccidioides posadasii targeting pyrG/URA3 so that 5-FOA can be used for selection pressure instead of traditional antibiotic...
16 February 2021 169 4 View
Is it related to nutrition or any other reason? Any other fungus have similar kind of growth pattern?
09 February 2021 4,357 4 View
Hello everyone, For my research I want to infect Vitis Vinifera leaves with downy mildew-causing fungus Plasmopara viticola. Does anyone know where I could find or purchase this fungi? I am...
04 February 2021 5,720 3 View
31 January 2021 1,832 17 View
I got my fungi sequences back from Illumina Miseq sequencing and I'm wondering how many reads do you use as a cutoff? ie. do you delete anything with less than 100 reads? I can't seem to find any...
28 January 2021 5,646 4 View