From: Suitable housekeeping genes for normalization of transcript abundance analysis by real-time RT-PCR in cultured bovine granulosa cells during hypoxia and differential cell plating density
Step
Description
Temperature
Time
1
Pre-incubation
95°C
5Â min
2
Denaturation
20Â sec
3
Annealing
60°C
15Â sec
4
Extension
72°C
5
Melting
5Â sec
70°C
60Â sec
97°C
1Â s (continuous acquisition)