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R5000

Ribonuclease A from bovine pancreas

Type II-A, ≥60% (SDS-PAGE), >= 60 Kunitz units/mg protein

Synonyma:

Pancreatic Ribonuclease, RNAsea, RNase A, Ribonucleate 3′-pyrimidinooligonucleotidohydrolase

Přihlásit pro zobrazení organizačních a smluvních cen.

Vybrat velikost

Změnit zobrazení
Vám/SKUDostupnostCena
100 mg
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3 640,00 Kč
250 mg
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5 870,00 Kč
1 g
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18 100,00 Kč

O této položce

Číslo CAS:
NACRES:
NA.54
UNSPSC Code:
12352204
EC Number:
232-646-6
MDL number:
Číslo EC:
Specific activity:
>= 60 Kunitz units/mg protein
Biological source:
bovine pancreas
Concentration:
≥60% (SDS-PAGE)

3 640,00 Kč


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biological source

bovine pancreas

Quality Segment

type

Type II-A

form

solid

specific activity

>= 60 Kunitz units/mg protein

mol wt

~13,700

concentration

≥60% (SDS-PAGE)

technique(s)

cell based assay: suitable

impurities

salt, essentially free

input

general use sample(s)

suitability

suitable for molecular biology

application(s)

diagnostic assay manufacturing

storage temp.

−20°C

SMILES string

[nH]1cnc(c1)CC(NC(=O)CCN)C(=O)O

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

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.
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.

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.
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 hybridase activity of human ribonuclease-1. Ribonuclease A from bovine pancreas has also been used in a study to investigate particle-based and monolithic columns for cation exchange protein displacement chromatography.

Features and Benefits

Our highly stable Ribonuclease A, RNase A, is suitable for removal of RNA, RNA sequencing, and DNA purification.

Preparation Note

Chromatographically purified

Analysis Note

Protein determined by E.
RNase A purity determined by SDS-PAGE

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Tato položka
R5500R4642R4875
description

Type II-A, ≥60% (SDS-PAGE), >= 60 Kunitz units/mg protein

description

Type XII-A, ≥90% (SDS-PAGE), 75-125 Kunitz units/mg protein

description

(Solution of 50% glycerol, 10mM Tris-HCL pH 8.0)

description

Type I-A, powder, ≥60% RNase A basis (SDS-PAGE), ≥50 Kunitz units/mg protein

biological source

bovine pancreas

biological source

bovine pancreas

biological source

bovine pancreas

biological source

bovine pancreas

technique(s)

cell based assay: suitable

technique(s)

cell based assay: suitable

technique(s)

-

technique(s)

cell based assay: suitable

specific activity

>= 60 Kunitz units/mg protein

specific activity

75-125 Kunitz units/mg protein

specific activity

-

specific activity

≥50 Kunitz units/mg protein

form

solid

form

lyophilized powder

form

(Solution of 50% glycerol, 10mM Tris-HCL pH 8.0)

form

powder

suitability

suitable for molecular biology

suitability

suitable for mRNA or total RNA extracted from cells and tissues

suitability

suitable for

suitability

suitable for molecular biology

concentration

≥60% (SDS-PAGE)

concentration

-

concentration

20-40 mg/mL

concentration

≥60% (RNase A, SDS-PAGE)


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Piktogramy

Health hazard

Výstražné slovo

Danger

Kódy nebezpečí

Bezpečnostní pokyny

Hazard Classifications

Resp. Sens. 1

Skladovací třída

11 - Combustible Solids

Co se děje?

WGK 3

Bod vzplanutí (°F)

Not applicable

Bod vzplanutí (°C)

Not applicable

PPE (osobní ochranné prostředky)

Eyeshields, Gloves, type N95 (US)



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