Nucleic acid methods
Nucleic acid methods are the techniques used to study nucleic acids: DNA and RNA.
Purification[]
- DNA extraction
- Phenol–chloroform extraction
- Minicolumn purification
- RNA extraction
- Boom method
- Synchronous coefficient of drag alteration (SCODA) DNA purification
Quantification[]
- Abundance in weight: spectroscopic nucleic acid quantitation
- Absolute abundance in number: real-time polymerase chain reaction (quantitative PCR)
- High-throughput relative abundance: DNA microarray
- High-throughput absolute abundance: serial analysis of gene expression (SAGE)
- Size: gel electrophoresis
Synthesis[]
- De novo: oligonucleotide synthesis
- Amplification: polymerase chain reaction (PCR)
Kinetics[]
- Multi-parametric surface plasmon resonance[1][2]
- Dual-polarization interferometry[3]
- Quartz crystal microbalance with dissipation monitoring (QCM-D)[4]
Gene function[]
Other[]
- Bisulfite sequencing
- DNA sequencing
- Expression cloning
- Fluorescence in situ hybridization
- Lab-on-a-chip
- Comparison of nucleic acid simulation software
- Northern blot
- Nuclear run-on assay
- Radioactivity in the life sciences
- Southern blot
- Differential centrifugation (sucrose gradient)
- Toeprinting assay
- Several bioinformatics methods, as seen in list of RNA structure prediction software
See also[]
- CSH Protocols
- Current Protocols
DNA Extraction Kits[]
There are commercially available DNA extraction kits for variety of biological samples, one such kit is the Taqgen® Blood Genomic DNA Kit, which is suitable for Genomic DNA Extraction from whole Blood, body fluids, buccal swabs, buffy coat and cultured cells. It is a spin column based kit, provide an easy, rapid and efficient purification of high quality genomic DNA. The purified DNA can be used directly in a variety of downstream applications, including PCR, Real-time PCR, southern blotting and restriction enzyme digestion. The kit eliminates the need for expensive resin, toxic phenol-chloroform extractions, or time-consuming alcohol precipitation. The standard procedure takes less than 20 minutes following cell lysis and yield purified DNA greater than 30 Kb in size.
https://en.wikipedia.org/wiki/DNA_extraction
How to extract DNA from Dried blood card?[]
Taqgen® Tissue DNA Kit 20 Preps [[1]]
References[]
- ^ Tang, Wei; Hu, Shichao; Wang, Huaming; Zhao, Yan; Li, Na; Liu, Feng (23 September 2014). "A universal molecular translator for non-nucleic acid targets that enables dynamic DNA assemblies and logic operations". Chem. Commun. 50 (92): 14352–14355. doi:10.1039/C4CC07041K. PMID 25295484.
- ^ Ihalainen, Petri; Pettersson, Fredrik; Pesonen, Markus; Viitala, Tapani; Määttänen, Anni; Österbacka, Ronald; Peltonen, Jouko (7 March 2014). "An impedimetric study of DNA hybridization on paper-supported inkjet-printed gold electrodes". Nanotechnology. 25 (9): 094009. Bibcode:2014Nanot..25i4009I. doi:10.1088/0957-4484/25/9/094009. PMID 24522116.
- ^ Berney, H.; Oliver, K. (2005). "Dual polarization interferometry size and density characterisation of DNA immobilisation and hybridisation". Biosensors and Bioelectronics. 21 (4): 618–626. doi:10.1016/j.bios.2004.12.024. PMID 16202875.
- ^ Dixon, Matthew C. (July 2008). "Quartz Crystal Microbalance with Dissipation Monitoring: Enabling Real-Time Characterization of Biological Materials and Their Interactions". Journal of Biomolecular Techniques. 19 (3): 151–158. PMC 2563918. PMID 19137101.
- ^ Hannon, Gregory J. (July 2002). "RNA interference". Nature. 418 (6894): 244–251. Bibcode:2002Natur.418..244H. doi:10.1038/418244a. ISSN 1476-4687. PMID 12110901. S2CID 4426281.
External links[]
- Genetics techniques
- Molecular biology
- Nucleic acids