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Vaccinia Capping Enzyme

For research use only. Not intended for any clinical use.
Cat.No.
RSNK-022
Description
Vaccinia Capping Enzyme is a recombinant protein from Vaccinia virus. Vaccinia Capping Enzyme can add 7-methylguanylate cap structure (Cap 0) to the 5' end of RNA. In eukaryotes, these terminal cap structures are involved in stabilization, transport, translation of mRNAs. Vaccinia Capping enzyme is composed of two subunits (D1R, D12L), and has three enzymatic activities (RNA triphosphatase, guanylyltransferase by the D1R subunit and guanine methyltransferase by the D12L subunit). All necessary for addition of a complete Cap 0 structure, m7Gppp5'N). In vitro, transcripts can be capped in the presence of reaction buffer, GTP, and the methyl donor (SAM).
Applications
• Labeling 5´ end of mRNA.
• Capping mRNA prior to translation assays/in vitro translation.
Buffer
10X VCE Capping Buffer
Concentration
25U/μL
Features
• Convenient solution that includes all components required for Enzymatic capping System based on the Vaccinia virus Capping Enzyme (VCE).
• Isolated form a recombinant source.
• Extensively quality controlled: Endo/Exonucleases/RNAses free.
Purity
>95%
Quality
Quality Test includs: Activity, SDS-PAGE/purity, DNase, RNase, endonuclease, transcription.
Size/Form
500U, 1000U, 2000U, 2500U
Source
Recombinant E.coli
Storage
-20°C

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Q & A

Customer Reviews

Customer Q&As
What is DNase I?

A: DNase I, also known as Deoxyribonuclease I, is an enzyme that plays a crucial role in the body. Its main function is to cleave DNA into small fragments by breaking phosphodiester bonds.

What is the role of DNase I?

A: Deoxyribonuclease I (DNase I) enzymes cleave single or double-stranded DNA and require divalent metal ions to hydrolyze DNA yielding 3΄-hydroxyl and 5΄-phosphorylated products.

Why is DNase used in RNA isolation?

A: DNase is used in RNA isolation to degrade any contaminating DNA that may be present in the sample. The presence of DNA can interfere with downstream applications such as reverse transcription or quantitative PCR. By treating the sample with DNase, researchers can ensure that only RNA is present in their sample.

Does your DNase I, RNase-free have any tags?

A: This product has no tags.

What is the best way to remove DNase I from my reaction?

A: The best way to remove DNase I from a reaction is by phenol/chloroform extraction or using a spin column. You can perform a heat inactivation step, but this may not completely remove all DNase I and may interfere with your downstream applications.

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Customer Reviews
Great!

DNase I (RNase-free) is ideal for removing contaminating genomic DNA from RNA samples.

United States

08/23/2020

Low risk

DNase I (RNase Free) is produced through a completely animal component-free process to eliminate any risks associated with animal-derived materials.

United States

05/12/2021

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