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Invitrogen™ SuperScript™ VILO™ Master Mix Non-distribution product as customer accommodation.

Deliver unprecedented linearity across the broadest range of input material and increased dynamic range for your quantitative RT-PCR (qRT-PCR) assays

Manufacturer:  Invitrogen 11755050

Catalog No. 11-755-050

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For Research Use Only. Not for use in diagnostic procedures.

Includes: (200µL) SuperScript™ III RT, RNaseOUT™ , Recombinant Ribonuclease Inhibitor, a proprietary helper protein, random primers, MgCl2, and dNTPs.



SuperScript™ VILO™ Master Mix is a robust reverse transcriptase premix containing everything you need for reverse transcription (RT) in one tube. SuperScript™ VILO™ (Variable Input, Linear Output) Master Mix pairs our tried and tested SuperScript™ III Reverse Transcriptase with enhanced buffer and RNaseOUT™ Recombinant Ribonuclease Inhibitor to enable reliable first-strand synthesis and higher cDNA yields from a wide range of input RNA concentrations.

  • Sensitive: linearity from 1pg to 2.5µg in a 20µL reaction
  • Convenient: single-tube format, just add your RNA and go
  • Flexible: suitable for qPCR detection methods such as SYBR™ Green and TaqMan™ assays
  • Powerful: high yields of cDNA

Consistent results from a variety of input RNA concentrations
The SuperScript™ VILO™ Master Mix provides the high-temperature capability of SuperScript™ III Reverse Transcriptase in an optimized format. The SuperScript™ VILO™ Master Mix can generate first-strand cDNA for use in real-time quantitative RT-PCR (qRT-PCR) with very low and very high amounts of input RNA (up to 2.5µg total RNA in a 20µL reaction).

Reliable, RNA-protected, reverse transcripition from total RNA
Because SuperScript™ III RT is not significantly inhibited by ribosomal and transfer RNA, it can be used to synthesize cDNA from total RNA. The SuperScript™ VILO™ Master Mix also includes RNaseOUT™ Recombinant Ribonuclease Inhibitor to safeguard against the degradation of target RNA due to ribonuclease contamination. Robust SuperScript™ III RT can be used to synthesize cDNA at a temperature range of 42–55°C.

Broad linearity for less template dilutions
Obtain the same relative representation in your cDNA qPCR template, regardless of gene abundance. During normalization, get both your gene of interest and the reference gene in a linear phase for cDNA synthesis even if their abundances differ in the starting material.

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