T4 Polynucleotide Kinase (10 U/μL)

SKU:BHZ20800043 Enzymes & Molecular Biology
Overview
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T4 Polynucleotide Kinase (T4 PNK) is a 5'-hydroxyl kinase that facilitates the transfer of the γ-phosphate from ATP to the 5'-hydroxyl termini of oligo- or polynucleotide chains, including double-stranded and single-stranded DNA or RNA, as well as to 3'-monophosphate nucleotides. This transfer is re
Enzyme Type Kinases & Phosphatases
Grade RUO
Storage -20°C
Shipping Dry Ice
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options:
    • Size (3) - 500 U, 2500 U, 10000 U
  • Lead time: options listed in "Availability Content"; otherwise, there will be a column of "lead time", other statuses may take longer.
  • Storage: -20°C
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Options selector
Catalog no. Size
12902ES76 500 U
12902ES86 2500 U
12902ES92 10000 U
Field Specification
Product Type
  • Enzymes
  • Kinases & Phosphatases
Shipping Dry Ice
Source Recombinant (E. coli)
Storage -20°C

T4 Polynucleotide Kinase (T4 PNK) is a 5'-hydroxyl kinase that facilitates the transfer of the γ-phosphate from ATP to the 5'-hydroxyl termini of oligo- or polynucleotide chains, including double-stranded and single-stranded DNA or RNA, as well as to 3'-monophosphate nucleotides. This transfer is reversible. T4 PNK also possesses 3'-phosphatase activity, which dephosphorylates 3'-phosphorylated oligonucleotide termini, deoxy 3'-monophosphate nucleotides, and deoxy 3'-diphosphate nucleotides. In the presence of ADP, T4 PNK can act as a 5'-phosphatase, promoting the exchange of 5'-phosphate groups on 5'-phosphorylated oligo-or polynucleotides with ATP. This enzyme is widely used for the construction of DNA libraries and for end labeling to generate probes.

Applications

Phosphorylation of the 5' ends of DNA or RNA for subsequent ligation

Terminal labeling of DNA or RNA to serve as probes and for sequencing purposes

5' phosphorylation of mononucleotides with a phosphorylated 3' end to prepare pNp substrates for attachment to the 3' ends of DNA or RNA

Labeling the 5' ends of oligonucleotides that possess a 3' phosphate group

Specifications

Source

Bacteriophage T4

Molecular weight

36.78 kDa

Concentration

10 U/μL

Unit definition

One unit is defined as the the amount required to catalyze the incorporation of 1 nmol of [γ-32P] ATP into a reaction within 30 minutes at 37°C

Glycerol Content

Contains Glycerol

Components

Components No.

Name

12902ES76

12902ES86

12902ES92

12902-A

T4 polynucleotide Kinase(10 U/μL)

50 μL

250 μL

1 mL

12902-B

10×T4 PNK Buffer

500 μL

1 mL

2×1 mL

[Note]: The 10×T4 PNK Buffer does not contain ATP; customers need to add it themselves, with a reference final concentration of 1 mM, or use the T4 DNA ligase buffer.

Shipping and Storage

This product should be stored at -25 ~ -15℃ for 1 year.

Store this enzyme at -20°C and avoid repeated freeze-thaw cycles to preserve catalytic activity. The product is shipped Dry Ice and remains stable for up to one year from the date of manufacture when stored under recommended conditions. Aliquoting the stock solution into single-use volumes is recommended for enzymes used infrequently to minimize thermal cycling of the bulk stock.

Phosphorylation of the 5' ends of DNA or RNA for subsequent ligation Terminal labeling of DNA or RNA to serve as probes and for sequencing purposes 5' phosphorylation of mononucleotides with a phosphorylated 3' end to prepare pNp substrates for attachment to the 3' ends of DNA or RNA Labeling the 5' ends of oligonucleotides that possess a 3' phosphate group. Always verify compatibility with your specific template, buffer, and downstream workflow.

One unit (U) is defined as the amount of enzyme that catalyzes the phosphorylation or dephosphorylation of 1 nmol of substrate per minute at 37°C under standard buffer conditions.

This enzyme is produced as Recombinant (E. coli) and supplied as a Research Use Only (RUO) reagent. Each lot is subjected to activity assay, purity assessment by SDS-PAGE, and functional validation prior to release. A Certificate of Analysis (CoA) and Safety Data Sheet (SDS) are available on request.

T4 Polynucleotide Kinase (T4 PNK) catalyzes the transfer of a γ-phosphate from ATP to the 5′-hydroxyl terminus of DNA or RNA, enabling ligation of blunt-end or cohesive-end fragments lacking 5′ phosphates. Shrimp Alkaline Phosphatase (SAP) removes 5′ and 3′ phosphate groups from DNA, RNA, and dNTPs, and is heat-inactivated at 65°C for 15 min—eliminating the need for column cleanup prior to downstream reactions.

Yeasen Biotechnology supports custom enzyme solutions across multiple service lines — from GMP-grade bulk supply to directed enzyme engineering. Contact BioHippo to discuss requirements and initiate a project inquiry.

▶ GMP-Grade & Bulk Supply

Select Yeasen enzymes are available in GMP grade, manufactured in an ISO 13485-certified UCF.ME™ ultra-clean molecular enzyme facility with FDA Drug Master File (DMF) support.

  • GMP-grade release testing and CoA documentation
  • ISO 13485-certified production facility
  • Scalable from milligram to multi-gram quantities
  • Consistent lot-to-lot activity specifications

▶ Glycerol-Free & Custom Formulation

Glycerol-free enzyme formats are available for applications requiring lyophilization compatibility, liquid handling automation, or direct IVD master mix integration.

  • Glycerol-free liquid format (standard and custom buffers)
  • Lyophilization-ready enzyme preparation
  • Custom reaction buffer optimization for specific assay conditions
  • Compatible with freeze-drying workflows for point-of-care formats

▶ Molecular IVD RDC Service

Yeasen's Research and Development Contracting (RDC) team delivers end-to-end solutions for molecular diagnostic product development, covering enzyme selection through clinical validation support.

  • Enzyme selection and performance matching
  • Primer/probe design and reaction buffer optimization
  • Sensitivity, specificity, and precision validation studies
  • Stability studies and SNP evaluation
  • Instrument platform compatibility assessment

▶ ZymeEditor™ Enzyme Engineering

Yeasen's proprietary ZymeEditor™ directed evolution and rational design platform enables the development of custom enzyme variants with tailored performance characteristics not available in off-the-shelf products.

  • Directed evolution for enhanced thermostability, processivity, or fidelity
  • Rational design for altered substrate specificity or cofactor requirements
  • Library screening from Yeasen's proprietary enzyme variant collection
  • Scale-up to commercial quantities upon candidate confirmation

ⓘ Customization services are fulfilled by Yeasen Biotechnology. Lead times and minimum order quantities vary by service type. Contact BioHippo for project scoping and pricing.

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