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Ribonucleoside vanadyl complexes

200 mM


Quality Level


200 mM

shipped in

dry ice

storage temp.


Related Categories

General description

Ribonucleoside vanadyl complexes are stable complexes formed between ribonucleotides. They are low molecular weight inhibitors of cellular ribonucleases (RNases) that are used for the isolation of RNA from cells.


Ribonucleoside vanadyl complexes are used as ribonuclease inhibitors during cell lysis and mRNA purification, to protect mRNA during cDNA production, and to protect RNA during digestion of DNA by DNaseI.
Ribonucleoside vanadyl complexes has been used:
  • as a component of lysis buffer for cell lines prior to Poly(U) pull down assay
  • to inhibit nucleases prior to immunoprecipitation (IP) of m6A-containing RNA fragment
  • as a component of hybridization buffer for human retinal slices

Biochem/physiol Actions

Ribonucleoside vanadyl complexes (RVC) elicits antimicrobial functionality by inhibiting ribosomal subunit formation and suppressing the growth of Staphylococcus aureus and Escherichia coli. It is also used as a preservative solution for tissues.


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Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3

Storage Class Code

12 - Non Combustible Liquids



Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

SIRT1 functions as a negative regulator of eukaryotic poly (A) RNA transport
Shan P, et al.
Current Biology, 27(15), 2271-2284 (2017)
Transcriptome-wide mapping of N6-methyladenosine by m6A-Seq
Dominissini D, et al.
Test, 560, 131-147 (2015)
Inhibition of intractable nucleases with ribonucleoside--vanadyl complexes: isolation of messenger ribonucleic acid from resting lymphocytes.
S L Berger et al.
Biochemistry, 18(23), 5143-5149 (1979-11-13)
Effect of ribonucleoside-vanadyl complexes on enzyme-catalyzed reactions central to recombinant deoxyribonucleic acid technology.
R S Puskas et al.
Biochemistry, 21(19), 4602-4608 (1982-09-14)
Hyone-Myong Eun
Enzymology Primer for Recombinant DNA Technology (1996)

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