Thermo Scientific RNase A, DNase and protease-free is an endoribonuclease that specifically degrades single-stranded RNA at C and U residues. It cleaves the phosphodiester bond between the 5'-ribose of a nucleotide and the phosphate group attached to the 3'-ribose of an adjacent pyrimidine nucleotide.

RNase A (e.g., bovine pancreatic ribonuclease A: ) is one of the hardiest enzymes in common laboratory usage; one method of isolating it is to boil a crude cellular extract until all enzymes other than RNase A are denatured. It is specific for single-stranded RNAs.

QIAGEN Ribonuclease A (RNase A) is DNase-free and quality-controlled for use in plasmid purification procedures for the digestion of RNA. This ready-to-use solution has the same specifications as the RNase supplied in all QIAGEN plasmid DNA purification kits.

RNase A catalyzes the transphosphorylation and degradation of RNA. It was the first protein identified to exhibit DNA melting functionality. This enzyme binds to several binding sites on single stranded (ss) RNA polynucleotide chain before degrading it.

RNase A, or Ribonuclease A, is an endonuclease that catalyzes the degradation of RNA. This enzyme is primarily known for its ability to cleave single-stranded RNA, which is paramount in regulating RNA levels within cells.

RNase A (bovine pancreatic ribonuclease) is the founding member an extensive family of divergent proteins that share specific elements of sequence homology, a unique disulfide-bonded tertiary structure, and the ability to hydrolyze polymeric RNA.

Bovine pancreatic ribonuclease, also often referred to as bovine pancreatic ribonuclease A or simply RNase A, is a pancreatic ribonuclease enzyme that cleaves single-stranded RNA. Bovine pancreatic ribonuclease is one of the classic model systems of protein science. [ 1 ]

RNase A is an endoribonuclease that cleaves single-stranded RNA, specifically on the 3′ side of pyrimidine (cytosine and uracil) nucleotides (Py/pN). You might find these chapters and articles relevant to this topic.

RNase A removes RNA during the isolation procedures of plasmid and genomic DNA. It is supplied with 1–10 mg/mL by resuspending in 10 mM Tris-HCl (pH 7.5), 15 mM NaCl, 50% (v/v) glycerol or in TE buffer. One unit of activity is defined as the amount of enzyme which causes the hydrolysis of RNA to yield a velocity constant, k=1, at 25°C and pH 5.0.

Ribonuclease A (RNase A) is an endoribonuclease that cleaves single-stranded RNA at the 3´ end of pyrimidine residues, forming oligoribonucleotides having 3´-terminal pyrimidine-3´-phosphates. Pyrimidine-3´-monophosphates are also released by RNase A cleavage of adjacent pyrimidine nucleotides.