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Ribonuclease A from bovine pancreas

SIGMA/R5250 - Type X-A, ≥90% (SDS-PAGE), ≥70 Kunitz units/mg protein

Synonym: Pancreatic Ribonuclease; RNAsea; RNase A; Ribonucleate 3′-pyrimidinooligonucleotidohydrolase

CAS Number: 9001-99-4
MDL Number: MFCD00132181
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-R5250-100MG 100 mg
$314.00
1/EA
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45-R5250-250MG 250 mg
$635.00
1/EA
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45-R5250-500MG 500 mg
$1140.00
1/EA
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45-R5250-1G 1 g
$1910.00
1/EA
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RNAse catalyzes the endonucleolytic cleavage of RNA to yield nucleoside 3′-phosphates and 3′-phosphooligonucleotides ending in Cp or Up.

 

assay ≥90% (SDS-PAGE)
biological source bovine pancreas
foreign activity protease, essentially free
form buffered aqueous solution
InChI 1S/C9H14N4O3/c10-2-1-8(14)13-7(9(15)16)3-6-4-11-5-12-6/h4-5,7H,1-3,10H2,(H,11,12)(H,13,14)(H,15,16)
InChI key CQOVPNPJLQNMDC-UHFFFAOYSA-N
mol wt ~13,700
Quality Level 200 
SMILES string [nH]1cnc(c1)CC(NC(=O)CCN)C(=O)O
specific activity ≥70 Kunitz units/mg protein
storage temp. −20°C
type Type X-A
Analysis Note: Protein determined by E.
Analysis Note: RNase A purity determined by SDS-PAGE
Application: • RNase A is used to remove RNA from DNA plasmid and genomic DNA preparations and protein samples.
• RNase A is also used in RNA sequence analysis and protection assays.
• RNase A has been used as a tool for computer-aided drug design.
• RNase A supports the analysis of RNA sequences.
• RNase A hydrolyze RNA contained in protein samples.
• Purification of DNA is supported by RNase A.
Application: Ribonuclease A from bovine pancreas has been used to treat human glioblastoma U251 cell line prior to harvesting, for flow cytometry analysis, T suppressor cells and embryonic stem cell chromatin.
Application: Ribonuclease A is used to remove RNA from DNA plasmid preparations and protein samples. Ribonuclease A is used for RNase protection assays, to remove unspecifically bound RNA, analysis of RNA sequences, to hydrolyze RNA contained in protein samples, and the purification of DNA. Ribonuclease A from bovine pancreas has been used in a study to assess the mechanism of heavy metal ions on RNase activity. Ribonuclease A from bovine pancreas has also been used in a study to investigate the performance of oligomeric poly(diallyldimethylammonium chloride) as displacer for cation-exchange displacement chromatography of proteins.
Biochem/physiol Actions: The structure of Ribonuclease A (RNase A) comprises of four disulfide and catalytic triad of two histidines crucial for its functionality. RNase A displays three-dimensional domain swapping of the α-helical N-terminal and the C-terminal β-strand. It can exist as dimer or oligomers. The level of RNase is elevated in cancers and infectious diseases. RNase A family of enzymes serve as potential drug targets. The homolog and variants of RNase A are potential chemotherapeutic agents.
Features and Benefits: Our highly stable Ribonuclease A, RNase A, is suitable for removal of RNA, RNA sequencing, and DNA purification.
General description: Ribonucleases do not hydrolyze DNA, because the DNA lacks 2′-OH groups essential for the formation of cyclic intermediates. RNase can hydrolyze RNA from protein samples. Pancreatic RNase A specifically cleaves at the 3′-side of pyrimidine (uracil or cytosine) phosphate bonds. The ribonuclease (RNase) gene is mapped to human chromosome 14.
General description: RNase A, Ribonuclease A, is an endoribonuclease that cleaves the phosphodiester bonds of single strand RNA after pyrimidine nucleotides. It attacks at the 3′ phosphate end (For example pG-pG-pC-pA-pG will be cleaved to give pG-pG-pCp and A-pG). The highest activity is exhibited with single stranded RNA. RNase A is a single chain polypeptide containing 4 disulfide bridges. In contrast to RNase B, it is not a glycoprotein. Ribonucleases do not hydrolyze DNA, because the DNA lacks 2′-OH groups essential for the formation of cyclic intermediates. RNase A can also hydrolyze RNA from protein samples. RNase A can be inhibited by alkylation of His12 and His119 and activated by potassium and sodium salts. RNAse is inhibited in the presence of heavy metal ions. RNase is also inhibited competitively by DNA.
Physical form: Solution in 0.2 M sodium phosphate buffer, pH 6.4
Preparation Note: A further chromatographic purification of R5503 to yield essentially pure RNAse A
Symbol GHS08  GHS08
Signal word Danger
Hazard statements H334
Precautionary statements P261 - P284 - P501
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥90% (SDS-PAGE)
activity specific activity: ≥70 Kunitz units/mg protein
Storage Temp. −20°C
Enzyme Commission (EC) Number 3.1.27.5   ( BRENDA  | IUBMB  )
UNSPSC 12352204

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