RNase A (DNase free)
Endoribonuclease
Bovine pancreas
| Catálogo Nº | Apresentação | Preço (R$) | Comprar |
|---|---|---|---|
| EN-179S | 2 x 50 mg | Sob demanda | Adicionar ao Carrinho |
| EN-179L | 2 x 250 mg | Sob demanda | Adicionar ao Carrinho |
For general laboratory use.
Definição de unidade: 1 unit corresponds to the amount of enzyme which hydrolyses RNA at a rate constant k = 1 at 25°C and pH 5.0 (Kunitz-units).
Envio: shipped at ambient temperature
Condições de armazenamento: store at 2-8 °C
stock solutions in TE buffer should be aliquoted and stored at -20 °C
Validade: 12 months
Peso molecular: 13.7 kDa (monomer)
CAS#: 9001-99-4
Número CE: 232-646-6
Pureza: ≥ 90 % (ion exchange chromatography), salt free, chromatographically homogeneous lyophilisate
Forma: dry powder
Atividade:
≥ 80 Kunitz units/mg
Unit definition: 1 Kunitz unit is that amount of activity which is capable of causing within 1 minute a decrease in absorbance at
300 nm equivalent to the maximum possible change in a 0.05 % solution of yeast RNA at 25 °C, pH 5.0.
Formulários:
RNase protection assays
Remove unspecifically bound RNA
Analysis of RNA sequences
Hydrolyse RNA contained in protein samples
Purification of DNA
Descrição:
RNase A is an endoribonuclease that attacks at the 3'-phosphate of a pyrimidine nucleotide. The sequence of pG-pG-pC-pA-pG will be cleaved to give pG-pG-pCp and A-pG. The highest activity is exhibited with ssRNA.
RNase A is free of detectable DNase and protease activity, a heat treatment of the enzyme is not necessary before use.
Reaction conditions:
Working concentration: 1 - 100 μg/ml (depending on application)
The enzyme is active under a wide range of reaction conditions. At low salt concentrations (0 to 100 mM NaCl), RNase cleaves ss and dsRNA as well as the RNA strand in RNA-DNA hybrids. At NaCl concentrations of 0.3 M or higher, RNase A specifically cleaves ssRNA.
Stability:
RNase A is an extremely stable enzyme, remarkable resistant to heating. It renatures easily after treatment with most denaturing agents.
Inactivation:
Ribonuclease inhibitor, Vanadyl-ribonucleoside complexes, arabinonucleosides, Zn2+, Cu2+, penicillin, Vitamin B12, SDS, DEPC, 4 M guanidinium thiocyanate plus 0.1 M 2-mercaptoethanol. Most polyanions show some inhibitory effect. Inactivated by phenol/chloroform extraction.
Isoelectric point (pI): 9.6
Optimal pH: 7.0 (activity range 6 - 10)
Referências selecionadas:
Burell et al. (1993) Enzymes of Molecular Biology, Vol. 16: 263.
Asubel et al. (1994 - 2005) Current Protocols in Molecular Biology, vol. 1, John Wiley & Sons, Inc., Brooklyn, NY 3.13.1