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Placing a strip of eight PCR tubes into a thermal cycler
Placing a strip of eight PCR tubes into a thermal cycler
An older, three-temperature thermal cycler for PCR
An older, three-temperature thermal cycler for PCR
Ethidium bromide-stained PCR products after gel electrophoresis. Two sets of primers were used to amplify a target sequence from three different tissu
Ethidium bromide-stained PCR products after gel electrophoresis. Two sets of primers were used to amplify a target sequence from three different tissue samples. No amplification is present in sample #1; DNA bands in sample #2 and #3 indicate successful amplification of the target sequence. The gel also shows a positive control, and a DNA ladder containing DNA fragments of defined length for sizing the bands in the experimental PCRs.
DNA samples are often taken at crime scenes and analyzed by PCR.
DNA samples are often taken at crime scenes and analyzed by PCR.
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Simplified diagram
Simplified diagram
Impure DNA extracted from an orange
Impure DNA extracted from an orange
T7 RNA polymerase (blue) producing an mRNA (green) from a DNA template (orange)
T7 RNA polymerase (blue) producing an mRNA (green) from a DNA template (orange)
A current model of meiotic recombination, initiated by a double-strand break or gap, followed by pairing with an homologous chromosome and strand inva
A current model of meiotic recombination, initiated by a double-strand break or gap, followed by pairing with an homologous chromosome and strand invasion to initiate the recombinational repair process. Repair of the gap can lead to crossover (CO) or non-crossover (NCO) of the flanking regions. CO recombination is thought to occur by the Double Holliday Junction (DHJ) model, illustrated on the right, above. NCO recombinants are thought to occur primarily by the Synthesis Dependent Strand Annealing (SDSA) model, illustrated on the left, above. Most recombination events appear to be the SDSA type.