The largest database of trusted experimental protocols

Rt2first sybr green rox pcr master mix

Manufactured by Qiagen
Sourced in Germany

The RT2 first SYBR green/ROX PCR master mix is a ready-to-use solution for real-time PCR amplification of DNA sequences. It contains SYBR Green I dye for detection and ROX passive reference dye for normalization.

Automatically generated - may contain errors

3 protocols using rt2first sybr green rox pcr master mix

1

RNA Isolation and qPCR Analysis of RAW 264.7 and Aorta Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA from RAW 264.7 cells or aortas was isolated using an RNeasy minikit (74104; Qiagen, Venlo, the Netherlands). RNA (1 μg) was used to synthesize cDNA by reverse transcription with an RT2 first-strand kit (330401; Qiagen). Real-time PCR analysis was performed on an ABI 7300 system (Thermo Fisher Scientific) with RT2 first SYBR green/ROX PCR master mix (330530; Qiagen). Specific primers for each gene were purchased from Qiagen. Genes of interest were normalized to mouse β-actin.
+ Open protocol
+ Expand
2

B16-F10 Cell Total RNA Isolation and Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA from B16-F10 cells was isolated using an RNeasy minikit
(74104; Qiagen, Hilden, Germany). By reverse transcription with an
RT2 first-strand kit (330401; Qiagen, Hilden, Germany), RNA (1
μg) was used to synthesize cDNA. Real-time PCR analysis was performed on
an ABI 7300 system (Thermo Fisher Scientific, Waltham, MA) with RT2first SYBR green/ROX PCR master mix (330530; Qiagen, Hilden, Germany). Specific
primers for each gene were purchased from Qiagen. Genes of interest were
normalized to mouse β-actin.
+ Open protocol
+ Expand
3

B16-F10 Cell Total RNA Isolation and Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total RNA from B16-F10 cells was isolated using an RNeasy minikit
(74104; Qiagen, Hilden, Germany). By reverse transcription with an
RT2 first-strand kit (330401; Qiagen, Hilden, Germany), RNA (1
μg) was used to synthesize cDNA. Real-time PCR analysis was performed on
an ABI 7300 system (Thermo Fisher Scientific, Waltham, MA) with RT2first SYBR green/ROX PCR master mix (330530; Qiagen, Hilden, Germany). Specific
primers for each gene were purchased from Qiagen. Genes of interest were
normalized to mouse β-actin.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!