I have kits and stuff but I also want to try with the basic protocol. I found some different things like with phenol,chloroform or the other things but i am not sure if it can work against the N2a cells.
Even though ribosomal ITS as a universal barcode marker for fungi is still hampered by a few limitations, the ITS will remain as the key choice for fungal identification. I usually see the ITS 1F...
11 August 2020 3,597 10 View
I'd like to prepare a Lysozyme and Lysozyme Digestion Buffer (25mM Tris-HCL, pH 8.0, 2.5mM EDTA, 1% Triton X-100) for bacterial cell lysate with a final Lysozyme concentration of 20mg/mL. I need...
29 July 2020 2,818 2 View
There are some studies on fused drug molecules. Sultamicillin is one of the example for this type of prodrugs. The drug would be hydrolized and reveals two different active molecules which is...
18 April 2020 4,758 3 View
Hi, I have question which I could not find an appropriate answer. By default, each laser diffraction instrument plots PSD using different bin sizes on the x-axis. This means, using default...
21 October 2019 6,899 3 View
Hello, I constantly submit parallel jobs in a shared HPC cluster for my OpenFOAM flow simulations and like everyone else, I have to decide how many cores I need. Our cluster runs constantly over...
11 May 2019 8,329 6 View
I simulated a patch antenna. I saw that the best S11 value is at 5.9GHz but when I measured I saw that it works at 5.93 GHz. What can be the reason?
23 September 2017 9,104 2 View
I have primers and i think i have to lysis the N2a cells but after that i couldn't find any protocol like how much i must add for template or other things.
06 June 2017 8,442 3 View
I would like to learn drawing or getting centerline of a surface in Solidworks. I search on internet but I found limited information. I found a programs like VMTKLab.There is a section for...
12 May 2015 2,748 7 View
I'm targeting to deploy a mesh network and manually configure MANET routing protocols. I'm preparing scenarios, architectures, and hard devices needed to do that. Are there some step-by-step...
03 March 2021 1,931 5 View
I am on the lookout for the Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence. Does anyone know where I can find it? Thank you in advance
03 March 2021 3,568 1 View
I am going to have 3 different probes in my qPCR work that I am going to do. But I realized that the machine we have in the lab is a Rotor-Gene Q 2plex HRM Platform, saying it has green, yellow,...
01 March 2021 8,544 1 View
Hi Community, I'm facing the issue of integration/compiling a new routing protocol in a WSN simulator. The final goal is to successfully add, configure this routing protocol in hardware devices...
01 March 2021 9,332 6 View
We are preparing some experiments based on irradiating cells under different conditions in order to evaluate the effects in terms of DNA damage, genetic expression, etc. As our project is...
01 March 2021 3,355 3 View
28 February 2021 8,466 2 View
Hi I am a bit confused. They are asking me to find out the volume of DNA required in ul (a total of 30-100 ng for genomic DNA) from the DNA concentration in the nanodrop reading which was 404.8...
26 February 2021 5,029 2 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 trying to better understand the scope of DNA replication and sequencing errors, e.g. 1. I have seen similar error rates of 10e4 to 10e5 for cell & instrumental DNA replication,...
24 February 2021 4,397 3 View
I got a thin band and a thick band i guess it would be the genomic DNA and the 260/280 ratio is 3.
21 February 2021 6,523 6 View