DNA电泳
· Top 10 Fun Facts for DNA Electrophoresis (Produced from LTI)Useful tips for preparing agarose gel and electrophoresis · Agarose Gel Electrophoresis (LaboratoryExperiments.com)A basic and very useful protocol for gel preparation and electrophoresis. · Agarose Gel (John Garland)How to prepare stock solutions and agarose solution · Dissolving and Casting Agarose Gels (FMC)Very nice and detailed procedures for preparing gel and some basic knowledge about agarose gel · Agarose Gel Electrophoresis (Molecular Biology Cyberlab)Very basic and illustrated guide · Agarose Gel Electrophoresis (Julie B. Wolf, UMBC)Provides method in gel preparation, recipes of electrophoresis buffer and loading buffer... · Agarose Gel Electrophoresis (Frank Bottone, Jr.) · DNA Gel (Hoshi Lab)Offers detailed information about resolution of DNA with agarose gel, gel preparation and electrophoresis... · Agarose Electrophoresis (Chen)DNA electrophoresis, extraction and concentration determination. · Agarose Gel Electrophoresis (Roe, OU) · DNA Mobility in Gels (Roe, OU) · Trouble Shooting DNA Agarose Gels (LTI)No band, Smear, anomalies band migration? Find trouble shooting here · Elution of DNA fragments from agarose (Roe, OU) · DNA Extraction from Agarose Gel (Crawford Lab) · Beta-Agarase Gel Purification (Crawford Lab)Recovering DNA from Agarose gel using Beta-Agarase · Isolation of DNA from Acrylamide Gels (Schimenti Lab) · Elution of DNA Fragments from Polyacrylamide Gels (Molecular Genetics Rec Lab) Molecular Marker · DNA Fragment Length Standards (Molecular Genetics RecLab)Lists of DNA restriction fragment length of lambda and pBR322 DGGE · Denaturing Gradient Gel Electrophoresis (DGGE) (Donis-Keller lab)Denaturing gradient gels are used to detect non-RFLP polymorphisms. The small (200-700 bp) genomic restriction fragments are run on a low to high denaturant gradient acrylamide gel; initially the fragments move according to molecular weight, but as they progress into higher denaturing conditions, each (depending on its sequence composition) reaches a point where the DNA begins to melt. The partial melting severely retards the progress of the molecule in the gel, and a mobility shift is observed. It is the mobility shift which can differ for slightly different sequences (depending on the sequence, as little as a single bp change can cause a mobility shift). Alleles are detected by differences in mobility. DNA Staining · Methylene Blue DNA staining (Gerard Lazo)This method primarily eliminates the damage of DNA by uv irradiation. DNA isolated from methylaene blue stained gels should transform frozen competent E. coli cells on the order of 20-50 fold more efficiently than ethdium bromide isolated DNA. · Vacuum Drying Agarose Gels (FMC)Many people ask how to dry agarose gel, here is the answer In Gel Application A usr/localiety of enzymatic reactions can be performed in the presence of agarose. In-gel reactions are an alternative approach to standard DNA recovery techniques and provide a multitude of benefits. The use of in-gel reactions will not only save time, but eliminate potential sample loss during DNA recovery from an agarose gel (FMC) Migration TablesPreparation of Agarose Gel and Electrophoresis
Extraction of DNA From Agarose Gel
Extraction of DNA from Acrylamide Gels
Two Dimensional Gel Electrophoresis
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