QuantiMir™ Mouse U6 Reference Assays

Extend your QuantiMir Kit with additional mouse U6 non-coding small nuclear RNA reference assays.
  • Ready-to-use reference assay
  • Designed for use with the QuantiMir Kit
  • Suitable for high-throughput screening of clinical samples

Products

Catalog Number Description Size Price Quantity Add to Cart
RA420A-mU6 QuantiMir™ Mouse U6 Reference Assay 50 Assays $95.00
- +
Contact Us

Overview

Overview

Supporting your studies with ready-to-go reference assays QuantiMir™ is SBI's simple and robust technology for profiling miRNAs. For labs using our QuantiMir Kit who need additional mouse U6 snRNA assays, we offer this stand-alone set of 50 assays. Visit the QuantiMir page to order the complete kit. See all of our reference assays:
Catalog #Amplified small RNASpecies compatibility
RA420A-hU6Human U6Human
RA420A-miR-16miR-16Human, Mouse
RA420A-mU6Mouse U6Mouse
RA420A-RNU1RNU1 (U1)Human, Mouse, Rat, Monkey
RA420A-RNU43RNU43Human, Mouse, Rat
RA420A-rU6Rat U6Rat

How It Works

How the QuantiMir Kit Works

The QuantiMir Kit enables robust miRNA quantitation through a simple and efficient workflow Highly efficient poly-A tailing and reverse transcription in a single reaction tube provides uniform cDNA synthesis of miRNAs. The optimized reaction conditions and buffer components maximize cDNA yield when starting with several micrograms down to picograms of input total RNA. The universal 3′ tag sequence incorporated during reverse transcription enables easily scalable and accurate miRNA expression analysis by qPCR—profile thousands of different miRNAs from a single reverse transcription reaction.
  • Tag all small RNAs with a poly-A tail
  • Anneal an oligo-dT adaptor
  • Reverse transcribe to create first-strand cDNA
The result is a cDNA pool of anchor-tailed miRNAs that are ready for qPCR. Create custom miRNA assays To design your own miRNA assays, simply synthesize an oligo using the sequence of the mature miRNA you’d like to profile as the forward primer in your miRNA qPCR assay, and use with the universal reverse primer included in the QuantiMir Kit.

Supporting Data

Resources

Citations

We're sorry, an error has occurred while generating this content.

Products

Catalog Number Description Size Price Quantity Add to Cart
RA420A-mU6 QuantiMir™ Mouse U6 Reference Assay 50 Assays $95.00
- +
Contact Us

Overview

Overview

Supporting your studies with ready-to-go reference assays QuantiMir™ is SBI's simple and robust technology for profiling miRNAs. For labs using our QuantiMir Kit who need additional mouse U6 snRNA assays, we offer this stand-alone set of 50 assays. Visit the QuantiMir page to order the complete kit. See all of our reference assays:
Catalog #Amplified small RNASpecies compatibility
RA420A-hU6Human U6Human
RA420A-miR-16miR-16Human, Mouse
RA420A-mU6Mouse U6Mouse
RA420A-RNU1RNU1 (U1)Human, Mouse, Rat, Monkey
RA420A-RNU43RNU43Human, Mouse, Rat
RA420A-rU6Rat U6Rat

How It Works

How the QuantiMir Kit Works

The QuantiMir Kit enables robust miRNA quantitation through a simple and efficient workflow Highly efficient poly-A tailing and reverse transcription in a single reaction tube provides uniform cDNA synthesis of miRNAs. The optimized reaction conditions and buffer components maximize cDNA yield when starting with several micrograms down to picograms of input total RNA. The universal 3′ tag sequence incorporated during reverse transcription enables easily scalable and accurate miRNA expression analysis by qPCR—profile thousands of different miRNAs from a single reverse transcription reaction.
  • Tag all small RNAs with a poly-A tail
  • Anneal an oligo-dT adaptor
  • Reverse transcribe to create first-strand cDNA
The result is a cDNA pool of anchor-tailed miRNAs that are ready for qPCR. Create custom miRNA assays To design your own miRNA assays, simply synthesize an oligo using the sequence of the mature miRNA you’d like to profile as the forward primer in your miRNA qPCR assay, and use with the universal reverse primer included in the QuantiMir Kit.

Supporting Data

Citations

We're sorry, an error has occurred while generating this content.