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Invitrogen™ SuperScript™ IV VILO™ Master Mix

Catalog No. 11766500
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Kit with ezDnase
No. of Reactions:
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500 Reactions
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Catalog No. Includes No. of Reactions
11766500 Kit with ezDnase 500 Reactions
11756050 Kit only 50 Reactions
11756500 Kit only 500 Reactions
11766050 Kit with ezDnase 50 Reactions
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Catalog No. 11766500 Supplier Invitrogen™ Supplier No. 11766500
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SuperScript IV VILO (SSIV VILO) Master Mix, available with or without ezDNase, is a reaction master mix designed for fast, sensitive, and reproducible cDNA synthesis in RT-qPCR applications.

SuperScript IV VILO (SSIV VILO) Master Mix, available with or without ezDNase, is a reaction master mix designed for fast, sensitive, and reproducible cDNA synthesis in RT-qPCR applications. The inclusion of ezDNase enzyme further accelerates the RT-qPCR workflow through an extremely simplified genomic DNA removal step.

SuperScript IV VILO Master Mix features include:
• Fast RT reactions in just 10 minutes
• Convenient one-tube cDNA reaction master mix for two-step RT-qPCR
• High yields reduce Ct values by more than two cycles ahead of all other reverse transcription reagents
• Efficient reaction even with low template amounts and suboptimal purity samples
• gDNA removal in as few as two minutes (SSIV VILO Master Mix with ezDNase only)

SSIV VILO Master Mix elevates the trusted VILO technology to the next level with the highly processive and thermostable SuperScript IV Reverse Transcriptase and further optimized buffer. These components enable efficient cDNA synthesis at higher temperatures and in less time. SSIV VILO master mix provides superior cDNA yield and sensitivity even with suboptimal purity or scarce templates. It is your new tool for more efficient and reproducible RT-qPCR.

SuperScript IV VILO Master Mix with ezDNase is available for better removal of genomic DNA and to further accelerate the RT-qPCR workflow. The extremely simplified genomic DNA removal step dramatically reduces the time of the entire reverse transcription protocol and reduces possible variation in gene expression due to RNA loss or damage during conventional DNase treatment.

SSIV VILO master mix results in more cDNA in less time with less pipetting, less variation, less reaction inhibition, less gDNA interference, and with less sample than other cDNA synthesis kits or master mixes for RT-qPCR. Additional ezDNase may also be purchased separately.

Source
Purified from E. coli expressing the pol gene of M-MLV, modified to increase thermostability and half-life, processivity, inhibitor resistance, and to reduce RNase H activity

Performance and quality testing
Assayed for endodeoxyribonuclease, exodeoxyribonuclease, and ribonuclease, as well as yield and length of cDNA product

Specifications

Concentration 5X
Content And Storage

• SuperScript IV VILO Master Mix (2 x 1 mL)
• SuperScript IV VILO Master Mix 'No RT' Control (1 mL)
• ezDNase Enzyme (500 μL)
• 10X ezDNase Buffer (1 mL)
• Nuclease-free water (1.25 mL)

Store at -15°C to -25°C.

Detection Method qPCR
Format Master Mix
GC-Rich PCR Performance High
Reaction Speed 10 min.
Technique Reverse Transcription
Optimal Reaction Temperature 50°C
Quantity Each
Reverse Transcriptase SuperScript IV
Ribonuclease H Activity Reduced
Shipping Condition Dry Ice
For Use With (Application) Real Time PCR (qPCR)
Final Product Type First-Strand cDNA
No. of Reactions 500 Reactions
Reaction Format Master Mix
Reagent Type Reverse Transcription
Size (Final Product) Up to 10 kb
Starting Material RNA
Includes Kit with ezDnase
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Does the TaqMan Cells-to-CT Express Kit contain reagents for the removal of genomic DNA (gDNA)?

Yes, the TaqMan Cells-to-CT Express Kit includes Express ezDNase which can be added to the Express Lysis Solution for removal of gDNA during cell lysis. Express ezDNase is a double-strand specific, heat-labile DNase that will only digest gDNA, making it compatible with the downstream reverse transcription reaction. The enzyme is automatically inactivated during a heat kill step included in the reverse transcription program. To avoid the detection of gDNA, we recommend using a TaqMan Gene Expression Assay specifically designed to span an intron-exon boundary. Such assays are designated with an "_m1" suffix. More information can be found here.

In your SuperScript IV RT protocols, there is no ezDNase inactivation step. Will ezDNase be active to affect RNA or the RT reaction?

The Invitrogen ezDNase Enzyme is a novel DNase that is highly specific for double-stranded DNA. It has no activity on single-stranded DNA in RT reactions (primers or probes), or on RNA. The enzyme is also thermolabile—it is inactivated quickly at temperatures typical for the SuperScript IV RT reaction (e.g., 50 degrees C). The additional inactivation step is therefore not required for most RT-qPCR applications. If the RNA sample is to be used for RT-PCR of fragments ≥3 kb, incubate the sample for 5 minutes at 55 degrees C in the presence of 10 mM DTT to inactivate the enzyme.

Which SuperScript IV RT format do you recommend for real-time PCR applications?

For RT-qPCR applications we recommend using the Invitrogen SuperScript IV VILO Master Mix. The cDNA synthesis reaction setup with this master mix requires fewer pipetting steps and therefore reduces variation in the data. SuperScript IV RT, as a component of the master mix, offers the highest efficiency of cDNA synthesis step compared to competitors’ products.

Are there any significant changes in the SuperScript IV RT protocol compared to the SuperScript III RT protocol?

The only difference is that the incubation time for the reverse transcription reaction has been reduced to 10 minutes and inactivation time has been reduced to 5 minutes at 85 degrees C.

Can I get comparable cDNA yield and length using the SuperScript IV RT 10-minute protocol as when using the 50-minute protocol for SuperScript III RT?

When compared with SuperScript III RT (and other manufacturers’ RTs) in a synthesis reaction for a 9 kb cDNA, SuperScript IV RT performed successful synthesis in just 10 minutes and did so with comparable (or improved) yield (as shown by gel band density).

Do you offer a one-step RT-qPCR kit containing SuperScript IV RT?

SuperScript IV RT is not recommended for one-step RT-qPCR applications. However, it is included in end-point one-step RT-PCR kits: https://thermofisher.com/ssiv-onestep

For one-step RT-qPCR, we recommend SuperScript III Flash Reverse Transcriptase or TaqPath RT-qPCR Master Mix products.

What is the difference between SuperScript IV RT and the RT enzyme used in SuperScript IV VILO Master Mix?

The SuperScript IV VILO Master Mix contains SuperScript IV RT, a ribonuclease inhibitor, and a helper protein. The helper protein helps to increase the efficiency of the reverse transcription reaction and thus improve cDNA yield. This master mix formulation allows for a simpler reaction setup with less pipetting and less variation between samples.

There is no ezDNase enzyme inactivation step in the SuperScript IV VILO Master Mix protocol. Will active ezDNase enzyme affect my RNA or RT reaction?

The ezDNase enzyme is highly specific for double-stranded DNA and does not cause damage to RNA and single stranded DNA. The high specificity of its action makes the deactivation step largely irrelevant in the subsequent RT reactions. ezDNase enzyme can be inactivated at 55 degrees C incubation for 2 min if needed.

How many reactions of SuperScript IV VILO 'No RT' Control are included with the SuperScript IV VILO Master Mix?

50 reaction packs (Cat. Nos. 11756050 and 11766050) include 200 μL of 'No RT' Control sufficient for 50 reactions. 500 reaction packs (Cat. Nos. 11756500 and 11766500) include 1 mL of 'No RT' Control sufficient for 250 reactions.

Why did you use oligo (dT)18 plus random hexamer primers for SuperScript IV VILO Master Mix whereas the SuperScript VILO Master Mix contains only random hexamer primers?

This is to help ensure that the bias from using either oligo (dT)18 or random hexamer primers alone will be eliminated. Although the data indicates that using random hexamers alone enables quantitation just as good as the combination of the two primers, this may improve data quality.

How does SuperScript IV VILO Master Mix perform with GC-rich RNA templates?

SuperScript IV VILO Master Mix often permits better cDNA synthesis results compared to other cDNA synthesis kits and master mixes. It has increased thermostability, allowing the RT incubation temperature to be raised up to 65 degrees C to deal with the GC-rich or structurally complex RNA templates.

What is the recommended reaction temperature for SuperScript IV VILO Master Mix?

The recommended reaction temperature for SuperScript IV VILO Master Mix is 50 degrees C. For GC-rich or structurally complex RNA templates, RT incubation temperature may be increased up to 65 degrees C.

What are the key performance improvements of SuperScript IV VILO Master Mix over the SuperScript VILO Master Mix and SuperScript VILO kits?

SuperScript IV VILO Master Mix uses SuperScript IV Reverse Transcriptase (RT) in the optimized master mix formulation, whereas SuperScript VILO Master Mix and SuperScript VILO kits use SuperScript III Reverse Transcriptase. SuperScript IV RT has a significantly improved performance profile over SuperScript III RT in thermostability, sensitivity, yield, processivity, and the ability to synthesize cDNA efficiently from a wide variety of RNA samples, even those of suboptimal purity and integrity.

Which applications can SuperScript IV VILO Master Mix be used for?

SuperScript IV VILO Master Mix is an upgrade from SuperScript VILO Master Mix and cDNA Synthesis Kit. It is designed to be used for cDNA synthesis in the two-step RT-qPCR applications for gene expression analysis.


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