In molecular diagnostics, nucleic acid extraction is the foundation of reliable results. Among all critical reagents, Proteinase K plays a central role in ensuring efficient and intact DNA recovery.

Proteinase K, a robust serine protease derived from Candida species, is widely used to digest proteins and release nucleic acids from complex biological samples. By breaking down histones and other structural proteins, it enables gentle yet effective DNA extraction—avoiding the damage often caused by harsh physical disruption.

 

The Hidden Challenge: Background Contamination

In pathogen detection workflows, especially those involving clinical samples, contamination can significantly impact accuracy.

Residual host DNA, nucleases, or microbial background from reagents—particularly Proteinase K—can:

  • Interfere with downstream qPCR or NGS analysis
  • Reduce sensitivity in low-abundance pathogen detection
  • Lead to false positives or inconsistent results

This makes low-residue, high-purity Proteinase K essential for modern molecular diagnostics. 

Yeasen Low-DNA Proteinase K Solution (Cat#10410)

Yeasen has developed a next-generation Proteinase K solution with stringent quality control across raw materials, production processes, and environmental conditionsensuring ultra-low contamination levels.

Key Features

  • Ultra-low microbial background minimizes interference in pathogen detection
  • Low nuclease contamination protects DNA integrity
  • High specific activity improved digestion efficiency
  • Broad pH tolerance (7.012.0) flexible across workflows
  • Stable enzyme activity at room temperature

Performance Highlights

1. Stability

Maintains >90% relative activity after 1 year at 25°C

Figure 1. Stability at 25°C

 Figure 1. Stability at 25°C

2. Optimal Conditions

Peak activity at 65°C (pH 8.0)

Active across a wide pH range (7.012.0)

Figure 2. Optimal temperature Range

 Figure 2. Optimal temperature Range

Figure 3. Optimal pH Range

 Figure 3. Optimal pH Range

3. Background Contamination Testing

Applied in nucleic acid extraction across 6 sample types. Followed by NGS library prep and sequencing 45 common clinical pathogens showed extremely low detection signals, confirming minimal background interference

Figure 4. Background DNA Residue Assessment

 Figure 4. Background DNA Residue Assessment

NGS analysis demonstrates extremely low background microbial signals across 45 common pathogens, confirming minimal DNA contamination.

4. Superior Purity & Activity

Highest specific activity (984 U/mL) among tested products

Minimal DNase/RNase contamination, ensuring DNA integrity

Supplier

Specific Activity (U/mL)

DNase Status

RNase Status

Nickase Status

Supplier A

820

Pass (ND*)

Pass (ND*)

Not Detected

Supplier B

738

Pass (ND*)

Slight Contamination

Slight Contamination

Supplier C

918

Pass (ND*)

Slight Contamination

Severe Contamination

Supplier D

768

Pass (ND*)

Pass (ND*)

Trace Level

Supplier E

924

Pass (ND*)

Pass (ND*)

Trace Level

Supplier F

632

Pass (ND*)

Slight Contamination

Severe Contamination

Yeasen-10410ES

984

Pass (ND*)

Pass (ND*)

Trace Level

 

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