Plasmid extraction

Molecular work 01: Plasmid extraction:

For plasmids, gDNAs, RNAs etc extraction, nowadays, we use commercial kits. I do not know when we started using commercial kits, but in early 2000s, many laboratories still used non-commercial methods- lab made Sol I (lysozyme lysis buffer), II (Acid buffer) and III (Alkaline buffer), following Phenol, Chloroform, and Isopropanol clearance after extraction. The most successful companies for plasmid kits may be Quiagen and Macherey-Nagel. They have plasmid kids for Mini, Midi, Maxi, Giga, Endo toxin free! In my mind, MN yields were better than Quiagen, but Giga prep I have used only Qiagen kit, so I am not sure whether MN has Giga prep kits as well. Quiagen, Promega and MN are still the most successful companies I think. Quiagen’s market occupancy started before 2000 even in South Korea. Also someone who is old like me might know and used CsCl plasmid purification. What I learned first during my Master degree training, was plasmid purification using CsCl ultracentrifuge method. It was simple but took time. My Master degree mentor Dr. Seho Park preferred CsCl at that time. I do not know which method he likes currently.

A few years ago, I saw a biotech company where they work to make a plasmid isolation machine. I’m not quite sure whether they were successful. However, you may hear Thermo KingFisher Plasmid Pro that I never used on my hands. Also you may hear automated lab components provided from Molecular device. I am not sure how they are successful. Long time ago, we/some old generation like me still remember that even we manually moved PCR tubes from different temperature water baths to another for PCR reaction.

About the water

Last step is adding solution either TE (Tris EDTA) or water. I recommend that you have to keep in mind what you are doing, for the next steps, before adding either TE or water. Generally I recommend adding water for the next steps: Restriction enzyme treatment, in vitro (cell), and in vivo (animal) treatment etc. TE definitely is a good solution for storage, but if you keep your plasmid DNAs at -20 °C, they are really safe, not degrading. You also could aliquot them. Usually, if you use water, you could save/reduce amounts of restriction enzyme using small reaction volume. Endo toxin free molecular grade water is easy to purchase from Fisher.

GMP plasmids

Maybe some heard about GMP (Good manufacturing practice) plasmids. I just googled how many GMP plasmids supplying companies are globally. There are quite numbers of companies including Aldevron and Catalent.

48. 함께 / Together

함께 바라보고
함께 꿈꾸고
함께 나아갈 수 있는 사람을
만날 수 있기 바래요
길고도 짧은 길
재미있고, 아름답게
이해 하고 이해 받으면서 걷기 바래요.


Looking together
dreaming together
I hope you meet Someone, 
whom you can move forward with
I hope you walk with someone, understanding and being understood.
long and short way during your journey
Full with fun and beauty

46. 틀 / the norm

비가 와도 우산을 쓰지 말아 봐요

자리가 비어도 앉지 말아 봐요

가질수 있는 걸 놓쳐도 보아요

생각의 틀에서 벗어나 봐요

이것도 저것도 즐겨봐요

Even if it rains, don’t use an umbrella

Even if the seat is empty, don’t sit down.

Even if you have what you could have, Just miss it out  

Step outside the norm

Enjoy this and that 

Bioinformatics: Featurecount Install and more

Subhead-2.0.2

https://github.com/ShiLab-Bioinformatics/subread/releases

  1. wget https://github.com/ShiLab-Bioinformatics/subread/releases/download/2.0.2/subread-2.0.2-macOS-x86_64.tar.gz
  2. tar -xvf subread-2.0.2-macOS-x86_64.tar.gz
  3. mv -v subread-2.0.2-macOS-x86_64 apps/
  4. nano .zshrc
  5. add: Export PATH=$PATH:/Users/__/___/subread/bin
  6. get gif or make gif: https://useast.ensembl.org/Mus_musculus/Info/Index
  7. use eg) featureCounts -T 5 -a annotation-subread/mouse_ensembl/Mus_musculus.GRCm38.102.gtf  -o quants/KO_count_matrix.txt HISAT2/SRR2936859.bam HISAT2/SRR2936860.bam HISAT2/SRR2936861.bam HISAT2/SRR2936864.bam HISAT2/SRR2936865.bam
  8. Cat file | less
  9. Cat file | cut f1,7-10> new file (could rename of column in excel!!!)

reference:

https://rdrr.io/bioc/Rsubread/man/buildindex.html

https://github.com/ShiLab-Bioinformatics/subread/releases

HISAT2 Install and more

  1. Download -version HISAST2 2.2.1 OSX_X86_64 : https://daehwankimlab.github.io/hisat2/download/#version-hisat2-221
  2. Put everything proper location: eg) /Users/___/___/hisat2-2.2.1
  3. Add Path into .zshrc: export PATH=$PATH:/Users/___/___/hisast2-2.2.1
  4. Download reference seq: eg) wget  https://genome-idx.s3.amazonaws.com/hisat/mm10_genome.tar.gz
  5. Need unzip: eg) tar -xvf mm10_genome.tar.gz
  6. Run alignment: eg) hisat2 -q –rna-strandness R -x hISAT2/mm10/genome -U data/SRR2936865_trimmed.fastq.gz | samtools sort -o HISAT2/SRR2936865.bam

If you need some more help:

Installation:

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