RT-qPCR Extraction Control Red
Meridian’s RT-qPCR Extraction Control Red uses artificial micelles of a known concentration that contain quantitative PCR positive control RNA sequence (with no known homology to any organism, so that it does not interfere with the detection of the sample target RNA). Their composition closely resembles a test sample and serves as a full-process quantitative PCR positive control, monitoring the success of an RT-qPCR assay from lysis/extraction to reverse transcription and amplification.
RT-qPCR Extraction Control Red, MDX028
Available in 1 mL (500 Rxns) aliquots
RT-qPCR Extraction Control Red contains an internal control RNA sequence, with no known homology to any organism, in an artificial cell. The RT-qPCR Extraction Control is spiked in the with lysis buffer into the sample prior to RNA extraction. Following RNA extraction, the control mix (containing specific primers and probe (emission wavelength = 670nm)) is added to the extracted RNA prior to amplification. The detection of RT-qPCR Extraction Control acts as a PCR positive control and confirms the success of the extraction, reverse transcription, and amplification steps, avoiding the misinterpretation of a false negative result.
|Description||Control used to monitor the success of an RT-qPCR assay from lysis/extraction to amplification and reduces the chance of obtaining false negative results from the sample RNA.|
|Appearance||Clear, colorless solution|
|Internal Control RNA||In micells|
|Control Mix||Primers and Quasar® 670 labeled probe|
|Application||Probe-based, one-step RT-qPCR|
|Sample type||Tissue, cells|
|Mix stability||See outer label|
|Functionaity/ Consistency||Ct of 27 – 30. The difference between test and history is less than 1 Ct.|
FAQs: RT-qPCR Extraction Control
The benefit of the artificial RT-qPCR Extraction Control in evaluation of the extraction process is the possibility to validate sample extraction process. Signal derived from the RT-qPCR Extraction Control confirms the success of the extraction step and monitors co-purification of PCR inhibitors that may cause biased or PCR false negative results. Housekeeping genes or spike in controls do not monitor the whole extraction process, especially the lysis step and in the case of housekeeping genes, extraction efficiency and degraded samples as well as the possibility of the housekeeping gene expression level changing.
When performing RNA extraction, it is often advantageous to have an exogenous source of RNA template that is spiked into the sample prior to lysis. This control RNA is then co-purified with the sample RNA and can be detected as a PCR positive control for the whole extraction process.
Although it is not mandatory yet, regulators across the world are tightening up recommendations for the addition of internal controls, EU: IVDD to IVDR 2017/746 “Control materials with quantitative or qualitative assigned values intended for one specific analyte or multiple analytes shall be classified in the same class as the device.” MDSAP with FDA (“general controls ensuring effectiveness of the device”), TGA (“provisions for the user, at time of use, of device performance”), MHLW and ANVISA
The RT-qPCR Extraction Controls are in micelles and so care needs to be taken when handling them. We recommend storing the RT-qPCR Extraction Control at -80 ᵒC and adding it to the lysis buffer before adding to the sample.
The primers and probe for the RT-qPCR Extraction Controls are in the Control Mix.
The two colors are for the fluorescent dyes on the RT-qPCR Extraction Control probe. Control Mix Red (Cy5 – emission wavelength = 670nm) and Control Mix Orange (HEX – emission wavelength = 560nm). This allows you to chose one that will fit with your existing protocol in a multiplex RT-qPCR assay.
No, the RT-qPCR Extraction Control will work with commercially available silica-membrane extraction kits and CHELEX matrices and has been tested on a wide range of qPCR platforms.