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P5568

Sigma-Aldrich

Proteinase K aus Tritirachium album

≥500 units/mL, buffered aqueous glycerol solution

Synonym(e):

Endopeptidase K

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About This Item

CAS-Nummer:
EC-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352204
eCl@ss:
32160410
NACRES:
NA.54

Biologische Quelle

microbial (T.album
T. ALBUM)

Qualitätsniveau

Form

buffered aqueous glycerol solution

Mol-Gew.

28.93 kDa

Konzentration

≥10 mg/mL
≥500 units/mL

Methode(n)

DNA extraction: suitable

Lagertemp.

2-8°C

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Allgemeine Beschreibung

Proteinase K, an extracellular endopeptidase is synthesized by the mold, Tritirachium album Limber. Proteinase K belongs to a new subfamily of the subtilisins. It is a 277 amino acid protein and is characterized with an unhydrolyzed protein chain and autolyzed polypeptide chains.

Anwendung

Nützlich zur proteolytischen Inaktivierung von Nukleasen bei der Isolierung von DNA und RNA.
Entfernt Endotoxine, die an kationische Proteine wie Lysozym und Ribonuklease A binden.
Berichten zufolge nützlich für die Isolierung von Leber-, Hefe- und Mungbohnen-Mitochondrien
Bestimmung der Enzymlokalisierung auf Membranen
Behandlung von Paraffinschnitten zur Freilegung von Antigenbindungsstellen zur Antikörpermarkierung.
Verdauung von Proteinen aus Hirngewebeproben für Prionen in der TSE-Forschung.
Proteinase K from Tritirachium album has been used:
  • to break down cardiac muscle during histopathology studies
  • during the digestion of HEK-293 cells
Proteinase K from Tritirachium album has been used in in situ detection of DNA fragmentation and in proteolysis experiments to measure the structural flexibility of interleukin 1ra (IL-1ra).
The enzyme from Sigma has been used in the digestion of sealed cytosolic side out ER vesicles. It has been used to deproteinize dissected brain and/or whole pupae sections of honey bee prior to in situ hybridisation. This was done during the study of neuropeptide Y-like signaling, and nutritionally-mediated gene expression and behaviour in the honey bee.

Biochem./physiol. Wirkung

Proteinase K has a broad specificity and degrades many proteins even in the native state. It mainly cleaves the peptide bond adjacent to the carboxyl group of aliphatic and aromatic amino acids with blocked alpha-amino groups. The optimum pH is between 7.5-9.0 and the isoelectric point is 8.9. Ca2+ (1-5 mM) is required for activation. Proteinase K is inhibited by DIFP or PMSF.
Proteinase K ist eine stabile und hochreaktive Serinprotease. Ergebnisse von Kristall- und Molekularstrukturstudien lassen darauf schließen, dass das Enzym zur Subtilisin-Familie mit einer katalytischen Triade (Asp39-His69-Ser224) im aktiven Zentrum gehört. Es ist in einer Reihe von Umgebungen stabil: pH, Puffersalze, Detergenzien (SDS) und Temperatur. In Gegenwart von 0,1–0,5 % SDS bleibt Proteinase K aktiv und verdaut zahlreiche Proteine und Nukleasen in DNA-Präparationen, ohne die Integrität der isolierten DNA zu beeinträchtigen.

Einheitendefinition

One unit will hydrolyze urea-denatured hemoglobin to produce color equivalent to 1.0 μmole of tyrosine per min at pH 7.5 at 37 °C (color by Folin-Ciocalteu reagent).

Physikalische Form

Solution in 40% (v/v) glycerol containing 10 mM Tris-HCl, pH 7.5, with 1 mM calcium acetate.

Angaben zur Herstellung

Proteinase K in solution is stable over a pH range of 4.0-12.5 (optimum pH 8.0), and is also stable over the temperature range of 25°C to 65°C during use. At pH 8.0, solutions will be stable for at least 12 months at 4°C. At pH 4-11.5, solutions containing Ca2+ (1-6 mM) are expected to be stable for several weeks. An 80% ammonium sulfate suspension stored at 4°C is stable for at least 12 months.

Piktogramme

Health hazard

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Resp. Sens. 1

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Denaturant-Dependent Conformational Changes in a beta-Trefoil Protein: Global and Residue-Specific Aspects of an Equilibrium Denaturation Process
Latypov RF, et al.
Biochemistry, 48(46), 10934-10947 (2009)
Amino acid sequence of proteinase K from the mold Tritirachium album Limber
Jany KD, et al.
Febs Letters, 199(2), 139-144 (2001)
Carolina Rosa Gioda et al.
American journal of physiology. Heart and circulatory physiology, 298(6), H2039-H2045 (2010-03-23)
Thiamine is an important cofactor of metabolic enzymes, and its deficiency leads to cardiovascular dysfunction. First, we characterized the metabolic status measuring resting oxygen consumption rate and lactate blood concentration after 35 days of thiamine deficiency (TD). The results pointed
Role of apoptosis in erosive and reticular oral lichen planus exhibiting variable epithelial thickness
Brant JMC, et al.
Brazilian Dental Journal, 19(3) (2008)
S A Ament et al.
Insect molecular biology, 20(3), 335-345 (2011-02-26)
Previous research has led to the idea that derived traits can arise through the evolution of novel roles for conserved genes. We explored whether neuropeptide Y (NPY)-like signalling, a conserved pathway that regulates food-related behaviour, is involved in a derived

Artikel

Proteinase K (EC 3.4.21.64) activity can be measured spectrophotometrically using hemoglobin as the substrate. Proteinase K hydrolyzes hemoglobin denatured with urea, and liberates Folin-postive amino acids and peptides. One unit will hydrolyze hemoglobin to produce color equivalent to 1.0 μmol of tyrosine per minute at pH 7.5 at 37 °C (color by Folin & Ciocalteu's Phenol Reagent).

Proteinase K (EC 3.4.21.64) activity can be measured spectrophotometrically using hemoglobin as the substrate. Proteinase K hydrolyzes hemoglobin denatured with urea, and liberates Folin-postive amino acids and peptides. One unit will hydrolyze hemoglobin to produce color equivalent to 1.0 μmol of tyrosine per minute at pH 7.5 at 37 °C (color by Folin & Ciocalteu's Phenol Reagent).

Protokolle

Proteinase K (EC 3.4.21.64) activity can be measured spectrophotometrically using hemoglobin as the substrate. Proteinase K hydrolyzes hemoglobin denatured with urea, and liberates Folin-postive amino acids and peptides. One unit will hydrolyze hemoglobin to produce color equivalent to 1.0 μmol of tyrosine per minute at pH 7.5 at 37 °C (color by Folin & Ciocalteu's Phenol Reagent).

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