Hello
Do I need to have a 1-5 ug of total RNA to get good result from RACE by Invitrogen method?
The more total RNA you use, the better the result. So ideally use 5ug, but I've used 3ug to good effect before.
Thanks for the feedback. 3 ug seems to be a lot. So you reckon 1 ug would be insufficient?
Cheers
Although I've only had success with 3ug or more, 1ug might be okay, so give it a go if you don't have access to any more material.
Hello all I am currently preparing reagents for WMISH for a fish species and wondering what commercial products (Ab) are usually used to fluorscent label DIG-UTP? And if I want to label...
05 June 2019 10,089 1 View
Hello guys I intend to label mRNA sperm with ISH technique but couldn't find a relevant protocol. What do you think if I use ISH protocol used for cultured cells? I appreciate your feedback, in...
05 June 2019 3,462 2 View
I want to have PGC line from Gambusia
06 July 2017 5,040 0 View
Hello, I am currently having problems with RNA extraction. I am using mouse liver (C57BL6J), and I have extracted RNA from mouse liver before. Before this experiment, my final RNA pellets were...
11 August 2024 7,082 3 View
I have been doing the m6A dot blot for a while with no improvement, I am extracting the RNA, and I can see the dots although the three biological replicas give a different reading on the memberan...
10 August 2024 8,539 5 View
I've been performing RNA extraction on cotton petiole tissue for a few months now using the method described in the following paper, a derivative of the typical hot borate method...
08 August 2024 9,882 2 View
I am currently working on LncRNA; to know the lncRNA-protein interactions I want to do RNA pull down assay, so I need to design primers with T7 promoter. I need assistance in this regard.
07 August 2024 6,622 1 View
Recently, we observed that 99% of the sequences in our RNA-seq data corresponded to the E. coli genome. Despite multiple DNAse treatments after RNA extraction and ribosomal depletion, we were...
06 August 2024 807 3 View
I am planning to collect human fecal samples for metatranscriptomic analysis using MGI. These samples are from indigenous people living in a region with high temperatures. I will have access to a...
06 August 2024 1,367 3 View
I will be with my students collecting seaweed samples in a marine farm and later we will process this tissue for RNA isolation and further sequencing. Does anyone have tips on how to collect the...
04 August 2024 501 2 View
I have an RNA-seq data that I have analysed using Limma-voom and have extracted the gene IDs, log2FC and the p-values. At p value < 0.05, I have over 10,000 DEGs, however, when I run the GO...
31 July 2024 225 2 View
I am currently working on a project involving liposomes and need to determine the maximum volume of siRNA that can be added to a 2.5 mL liposome solution with a total lipid concentration of 10...
30 July 2024 6,420 1 View
Hello, I have a little problem. Well, right now I only have the DNA aptamer sequence. I went to see the 2D model form with DNA folding. After that, I used RNA Composer to simulate in 3D and used...
30 July 2024 6,794 0 View