Proteinase K, CAS No.39450-01-6

CAS: 39450-01-6 Cat. No.: P109033 EC Number: 254-457-8,3.4.21.64
AVAILABLE TO ORDER
GRADE & PURITY Bioactive ? Bioactive grade — verified to retain biological activity in functional assays. Use when the molecule must be functionally active, not just pure. Recombinant ? Recombinant — produced via recombinant expression for defined sequence and consistency. Use for reproducible, animal-free proteins of known origin. ActiBioPure™ ? ActiBioPure™ — Aladdin's premier line for bioactive and recombinant products. Use when both high purity and preserved biological activity are required. High Performance ? High-performance grade with optimized purity and performance characteristics. Use for sensitive analyses where ordinary grades fall short. EnzymoPure™ ? EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance. ≥95% lyophilized powder,≥30 units/mg protein;expressed in Pichia pastoris
Accession #
P06873
Expression system
Pichia pastoris
Bioactivity
≥30 units/mg protein
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Size
USA
Germany (EU)*
Price
Qty
25mg
P109033-25mg
2 In stock
—
$14.90
100mg
P109033-100mg
In stock ≥10
—
$29.90
500mg
P109033-500mg
In stock ≥10
—
$94.90
1g
P109033-1g
1 In stock
—
$171.90
5g
P109033-5g
Made to order · 8–12 wks
$683.90
25g
P109033-25g
1 In stock
—
$2,795.90
100g
P109033-100g
1 In stock
—
$8,799.90
Enter a quantity for the sizes you want to add.
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Why this grade

Bioactive,Recombinant,ActiBioPure™,High Performance,EnzymoPure™,≥95%,lyophilized powder,≥30 units/mg protein;expressed in Pichia pastoris ActiBioPure™,Bioactive,High Performance,Recombinant,EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 76 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

This product is derived from Pichia pastoris expressing the Proteinase K gene from Parengyodontium album (formerly known as Tritirachium album Limber) optimized by site-directed mutagenesis. It exhibits advantages including high specific activity, high yield, and a broader active temperature and pH range.
Advanced protein engineering technology and a 28,000-liter yeast fermentation platform enable efficient unit cost control, providing cost-effective Proteinase K for biopharmaceutical R&D and production. High-efficiency yeast expression and chromatographic purification ensure product purity. The product is endotoxin-free, with a wider range of applications than native Proteinase K.
As one of the highly active proteases available, Proteinase K displays activity over a pH range of 4–12 and a temperature range of 0–75 °C, and retains activity even in the presence of SDS, urea, or EDTA. Proteinase K cleaves peptide bonds at the carboxyl side of aliphatic and aromatic amino acids and is capable of degrading virtually all proteins.
Product Characteristics
Source organism: Pichia pastoris expressing the genetically engineered Proteinase K gene from Parengyodontium album
Molecular weight: 29.3 kDa
pI: 8.9
Applications
Used in gene diagnostic kits, genomic DNA extraction kits, and RNA extraction kits to remove nucleases and other protein contaminants;
Used in the biopharmaceutical industry for the extraction of non-protein biological products such as nucleic acids and polysaccharide drugs, e.g., the preparation of DNA vaccines and heparin;
Used in skin care for the removal of aged keratinocytes, as well as in daily industrial fields including leather tanning, production of hydrolyzed protein seasonings, cosmetics, and feed processing.

Specifications

Product Name
Proteinase K, CAS No.39450-01-6
Synonyms
(4-nitrophenyl)methyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-3,4-diphenoxy-5-phosphonooxy-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate | BP178285 | AKOS032949645 | Endopeptidase K | Protease K | Endoproteinase K | Endopeptidase K | peptidase K |
Grade
ActiBioPure™, Bioactive, High Performance, Recombinant, EnzymoPure™
Specifications & Purity
Bioactive,Recombinant,ActiBioPure™,High Performance,EnzymoPure™,≥95%,lyophilized powder,≥30 units/mg protein;expressed in Pichia pastoris
Biochemical and Physiological Mechanisms
Hydrolyzes keratin at aromatic and hydrophobic residues. Catalytic activity: Hydrolysis of keratin, and of other proteins with subtilisin-like specificity. Hydrolyzes peptide amides. Cofactor: Ca2+. Note: Binds 2 calcium ions per subunit.
Bioactivity
≥30 units/mg protein
Accession #
Predicted molecular weight
29.3 kDa
CAS
39450-01-6
Enzyme Commission Number
EC 3.4.21.64
Molecule Type
Enzyme
Storage and Shipping
Concentration
lyophilized powder,≥30 units/mg protein;expressed in Pichia pastoris
Reconstitution
Reconstitute in 20 mM Tris-HCl, 1 mM CaCl₂, pH 7.4.
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Unit definition
One unit is defined as the enzyme activity that produces 1 µmol of tyrosine per minute from casein at 37°C at pH 7.5.

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassLactams
SubclassBeta lactams
Intermediate Tree Nodes Not available
Direct ParentCarbapenems
Alternative Parents Benzyloxycarbonyls  Alpha amino acids and derivatives  Nitrobenzenes  Pyrroline carboxylic acids  Phenoxy compounds  Phenol ethers  Nitroaromatic compounds  Monoalkyl phosphates  Azepines  Alkyl aryl ethers  Vinylogous esters  Tertiary carboxylic acid amides  Enoate esters  Secondary alcohols  Azetidines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Monocarboxylic acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Carbapenem - Benzyloxycarbonyl - Alpha-amino acid or derivatives - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Phenol ether - Monoalkyl phosphate - Azepine - Alkyl aryl ether - Benzenoid - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Monocyclic benzene moiety - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tertiary carboxylic acid amide - Pyrroline - Organic nitro compound - Secondary alcohol - C-nitro compound - Carboxylic acid ester - Carboxamide group - Azetidine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as carbapenems. These are beta-lactam derivatives in which the beta-lactam ring shares the nitrogen atom with a pyrrole-2-carboxylic acid.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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66 results found

Lot NumberCertificate TypeDateItem
E2611500Certificate of AnalysisApr 28, 2026 P109033
E2611485Certificate of AnalysisApr 28, 2026 P109033
E2611501Certificate of AnalysisApr 28, 2026 P109033
E2611502Certificate of AnalysisApr 28, 2026 P109033
E2611503Certificate of AnalysisApr 28, 2026 P109033
E2611504Certificate of AnalysisApr 28, 2026 P109033
E2611505Certificate of AnalysisApr 28, 2026 P109033
D2423042Certificate of AnalysisJan 21, 2026 P109033
C2406012Certificate of AnalysisDec 12, 2025 P109033
A2419061Certificate of AnalysisOct 13, 2025 P109033
K2504562Certificate of AnalysisOct 10, 2025 P109033
K2504564Certificate of AnalysisOct 10, 2025 P109033
K2504563Certificate of AnalysisOct 10, 2025 P109033
K2504565Certificate of AnalysisOct 10, 2025 P109033
L2510557Certificate of AnalysisOct 10, 2025 P109033
L2510558Certificate of AnalysisOct 10, 2025 P109033
L2510559Certificate of AnalysisOct 10, 2025 P109033
L2510560Certificate of AnalysisOct 10, 2025 P109033
L2510561Certificate of AnalysisOct 10, 2025 P109033
K2504561Certificate of AnalysisOct 10, 2025 P109033
H2618176Certificate of AnalysisOct 10, 2025 P109033
L2510562Certificate of AnalysisOct 10, 2025 P109033
J2330021Certificate of AnalysisAug 07, 2025 P109033
J2311075Certificate of AnalysisJul 15, 2025 P109033
K2125249Certificate of AnalysisJun 17, 2025 P109033
E2520629Certificate of AnalysisApr 23, 2025 P109033
E2520631Certificate of AnalysisApr 23, 2025 P109033
E2520630Certificate of AnalysisApr 23, 2025 P109033
E2520628Certificate of AnalysisApr 23, 2025 P109033
E2520627Certificate of AnalysisApr 23, 2025 P109033
E2520626Certificate of AnalysisApr 23, 2025 P109033
D2627021Certificate of AnalysisApr 23, 2025 P109033
K2520216Certificate of AnalysisDec 26, 2024 P109033
A2521412Certificate of AnalysisDec 26, 2024 P109033
A2521370Certificate of AnalysisDec 26, 2024 P109033
A2521365Certificate of AnalysisDec 26, 2024 P109033
A2521363Certificate of AnalysisDec 26, 2024 P109033
A2521359Certificate of AnalysisDec 26, 2024 P109033
H2501076Certificate of AnalysisDec 26, 2024 P109033
G2412539Certificate of AnalysisJul 04, 2024 P109033
I2423642Certificate of AnalysisJul 04, 2024 P109033
I2419068Certificate of AnalysisJul 04, 2024 P109033
G2412554Certificate of AnalysisJul 04, 2024 P109033
G2412544Certificate of AnalysisJul 04, 2024 P109033
G2412543Certificate of AnalysisJul 04, 2024 P109033
G2412542Certificate of AnalysisJul 04, 2024 P109033
G2412541Certificate of AnalysisJul 04, 2024 P109033
G2412540Certificate of AnalysisJul 04, 2024 P109033
H2429117Certificate of AnalysisJul 04, 2024 P109033
C2406011Certificate of AnalysisJan 23, 2024 P109033
C2211247Certificate of AnalysisDec 19, 2023 P109033
C2211248Certificate of AnalysisDec 19, 2023 P109033
K2125251Certificate of AnalysisAug 21, 2023 P109033
K2125264Certificate of AnalysisAug 21, 2023 P109033
C2110015Certificate of AnalysisDec 13, 2022 P109033
C2110016Certificate of AnalysisDec 13, 2022 P109033
K2217188Certificate of AnalysisNov 29, 2022 P109033
C2303238Certificate of AnalysisSep 26, 2022 P109033
I2222451Certificate of AnalysisSep 26, 2022 P109033
K2024181Certificate of AnalysisSep 17, 2022 P109033
A2316087Certificate of AnalysisDec 25, 2021 P109033
C2211179Certificate of AnalysisDec 25, 2021 P109033
L2305179Certificate of AnalysisDec 25, 2021 P109033
G2314185Certificate of AnalysisDec 25, 2021 P109033
G2404076Certificate of AnalysisDec 25, 2021 P109033
A2303338Certificate of AnalysisDec 25, 2021 P109033
Documents & Articles
In Situ Hybridization (ISH) Protocol
Apoptosis DNA Fragmentation Analysis Protocol
Dual Cross-linking ChIP Protocol
Proteinase K and Ribonuclease A
Selection Criteria for Proteinase K
Three Main Differences Between AEBSF and PMSF Protease Inhibitors
Proteinase K: Frequently Asked Questions
Commonly Used Proteases in Research: Fundamentals and Representative Applications
Deoxyribonuclease (DNase): DNA Hydrolytic Cleavage Properties, Methodological Value, and Multi-Context Applications
Micrococcal Nuclease (MNase): A Technical Review of Enzymatic Properties, Reaction Control, and Research and Biomanufacturing Applications
dsDNase-Mediated Hydrolysis of Double-Stranded DNA: Enzymatic Characteristics, Methodological Strategies, and Bioanalytical Applications
Furin: A Review of Its Structural Features, Substrate Recognition, and Research Applications
Comparison of Low-pH, High-pH, and Enzymatic Antigen Retrieval Systems in IHC
Cell Apoptosis Detection by TUNEL Labeling: Signal Interpretation and Result Evaluation
β-Glucan Content Determination Methods, Sample Pretreatment and Quality Control
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
CRISPR/Cas9 and targeted genome editing
Advanced enzyme analysis technology
Protein sample preparation process
GITC——Key Reagent for Nucleic Acid Extraction and Sample Protection
Bacterial Cell Wall Degradation Technology
Functional Differences Between Endopeptidases and Exopeptidases and Their Applications in Disease Mechanism Research
Catalytic Mechanisms, Classification Characteristics, and Experimental Applications of Serine Endopeptidases
Citations of This Product
Solution Calculators
Reviews

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