Making RNA probes with T7 transcription: Difference between revisions
From OpenWetWare
Jump to navigationJump to search
line breaks |
back to protocols |
||
| Line 1: | Line 1: | ||
{{back to protocols}} | |||
== mRNA sense & antisense probes == | == mRNA sense & antisense probes == | ||
[[Image:Antisense_probes_and_mRNA.png|thumb|left|500px|Probes need to be antisense respective to the mRNA to be able to bind their target. Care has to be taken during experimental design to make a suitable antisense probe.]] | [[Image:Antisense_probes_and_mRNA.png|thumb|left|500px|Probes need to be antisense respective to the mRNA to be able to bind their target. Care has to be taken during experimental design to make a suitable antisense probe.]] | ||
Latest revision as of 15:33, 20 June 2009
| back to protocols | ||
mRNA sense & antisense probes

In vitro T7 transcription of an RNA probe

- designing a suitable primer combining the T7 promoter sequence and a sequence specific part
- attaching a T7 promoter via PCR
- in vitro transcription using T7 polymerase and the PCR product as a template