Blood and Tissue DNA Extraction: Introduction, Test Requirements, Procedure, and Keynotes
Blood for DNA Extraction
Introduction of Blood and Tissue DNA Extraction
Table of Contents
Advances in DNA technology have been created in the increased application of DNA tests. From paternity determination to criminal investigations and even disease diagnosis the accuracy and data provided mean that millions of people are now shifting to DNA testing to solve their questions.
Fig. Blood Collection for DNA Extraction
Test Requirements for Blood and Tissue DNA Extraction
DNA extraction kit and it contains-
Proteinase K
Lysis buffer (AL)
Wash solution (AW1)
Wash solution 2 (AW2)
Elution buffer(AE)
Spin column and collection tubes
Extra we need-
Ethanol (molecular grade)
Centrifuge tubes
Centrifuge
Short spinner
Micropipettes and tips
Waste bin
Tissue paper roll
Fig. EDTA Blood for DNA Extraction
DNA Extraction Procedure
Fig. Blood for DNA Extraction, Proteinase K and Lysis Buffer
Place 20 μL proteinase k in an Eppendorf tube of 1.5 ml and then put a 200 ul sample (blood).
Add 200 μL AL buffer and vortex for 15 seconds and incubate at 56 C for 10 minutes.
Perform a short spin.
Add 200 μL absolute ethanol of molecular grade and again vortex or short spin for 15 seconds.
Transfer the mixer to a spin column and centrifuge at 8000 rpm/ 6000g for a minute.
Transfer the column to the collection tube provided 500 ul AW1 and again centrifuged at 8000 rpm or 6000g for a minute.
Discard the collection tube.
Add 500 μL of AW2 and centrifuge at 14000 rpm for 3 minutes.
Discard the collection tube.
Transfer to a new 1.5 ml centrifuge tube.
Add 200 μL AE buffer and centrifuge at 8000 rpm for a minute.
This is a solution having DNA i.e. template.
Keynotes
Adding template for PCR amplification
The template should be used on the same day otherwise it should be stored as genomic DNA stored at -20°C and -80°C is of good quality, and these specimens withstand multiple freeze-thaw cycles.
DNA quality can be assessed by agarose gel electrophoresis, PCR amplification of an the indicator housekeeping gene (β-globin), and SNP assays on various platforms.
For short-term studies, genomic DNA can be stored at 4°C or even room temperature (RT) without degradation, but specimens should be monitored for DNA concentration and evaporation.
DNA Extractor Automations are also available in the market to minimize the cumbersome steps of manual extraction.
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Fascinating blog! Is your theme custom made or did you download it from somewhere? A theme like yours with a few simple adjustements would really make my blog jump out. Please let me know where you got your design. Thank you
Great post. I am facing a couple of these problems.
Normally I do not read article on blogs, but I wish to say that this write-up very forced me to try and do so! Your writing style has been amazed me. Thanks, quite nice post.
We are a group of volunteers and opening a new scheme in our community. Your website offered us with valuable info to work on. You've done a formidable job and our whole community will be grateful to you.
Very interesting topic, regards for posting.
Nice post. I was checking constantly this blog and I am impressed! Extremely helpful info specifically the last part :) I care for such info much. I was seeking this particular information for a very long time. Thank you and good luck.
I love your writing style truly enjoying this internet site.
You actually make it appear so easy along with your presentation but I in finding this matter to be actually something that I believe I'd by no means understand. It kind of feels too complex and very large for me. I'm having a look ahead for your subsequent post, I will try to get the cling of it!
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