A total of 20 [micro]g of crude venom and 10 [micro]g of venom fractions were separated under reducing-conditions in a 10-20% Tricine
acrylamide gel. The gel was run at 120V for 90 min using a BioRad PowerPak system.
NOTE: The main purpose of steps 4 and 5 is to observe the size and efficiency of PCR products amplified by different primer combinations and thus to estimate the electrophoresis time on 6% denaturing
acrylamide gels in the next step.
It does not require cDNA cloning and blotting and can even be applied in laboratories where radioactive labelling is not available by using the silver staining method that enables the detection and recovery of the PCR products from
acrylamide gels.
Concentrations of diffused solute from
acrylamide gel were measured using disodium fluorescein and GGR as chemical tracers in the field.
To confirm the results, PCR products were sequenced or separated on 10%
acrylamide gels.
In addition, there are no hazardous reagents such as ethidium bromide, which is commonly used to visualize restriction digestion products on agarose or
acrylamide gels. Moreover, because this method is sensitive and tolerates a broad range of DNA concentrations, there is a high rate for successful genotyping.
(1997) probably resulted from their use of
acrylamide gels for allele detection.
The globulins and prolamines were resolved with 120 g [kg.sup.-1] and 100 g [kg.sup.-1]
acrylamide gels, respectively.
High percentage
acrylamide gels improve resolution in SSCP analysis.
From these experiments it follows that PEG at 5 g/L is suitable for differential separation of single-stranded DNA fragments in the range of 150-528 nucleotides in 12%
acrylamide gels with %C = 2.5.
Acrylamide Gel electrophoresis of soluble plant proteins.
The PCR products were electrophoresed in 3.5% agarose gel or 10.0%
acrylamide gel (19:1 acrylamide/ bis-acrylamide) or 6.0% denaturing
acrylamide gel (19:1 acrylamide/bis-acrylamide, 6 M urea).