$507.00
The Avam® Klenow Fragment (3′→5′ exonuclease) enzyme provides a versatile solution for various molecular biology applications, characterized by its unique features and robust performance. Derived from DNA polymerase I, this fragment exhibits a deficiency in both proofreading (3′→5′) and nick-translation (3′→5′) nuclease activities, making it ideal for specific molecular biology techniques.
The enzyme retains its 3′→5′ DNA polymerase activity, ensuring efficient DNA synthesis, while lacking proofreading and nick-translation activities, which can be advantageous for certain applications. Its moderate strand displacement activity during DNA synthesis further enhances its utility in various experimental setups.
Supplied in a convenient formulation containing 20 mM Tris-HCl, 1 mM DTT, 0.1 mM EDTA, and 50% glycerol, the Avam® Klenow Fragment (3′→5′ exonuclease) is readily accessible for use in molecular biology laboratories. Additionally, it comes with a 10X Blue Buffer containing essential components such as NaCl, Tris-HCl, MgCl2, and DTT, ensuring optimal enzyme performance under diverse experimental conditions.
Performance-wise, the Avam® Klenow Fragment (3 exonuclease) demonstrates high purity (>90%) and specific activity (10,000 U/mg), along with minimal contaminating activities such as single-stranded and double stranded exonuclease, endonuclease, and E. coli DNA contamination, ensuring reliable and reproducible results.
The enzyme’s principle lies in its unique biochemical properties, where it lacks the 5′→3′ exonuclease activity present in DNA polymerase I, making it suitable for applications where this activity is undesirable. Instead, it retains the 5′→3′ polymerase activity and 3′→5′ exonuclease activity, essential for DNA synthesis and removal of precoding nucleotides, respectively.
Notably, the Avam® Klenow Fragment (3′→5′ exonuclease) finds widespread use in molecular biology serving as a preferred choice for DNA labeling, dA-tailing, and dT-tailing for next-generation sequencing adapter ligation. Additionally, it finds applications in dideoxy DNA sequencing, cDNA second shand synthesis, and site-directed DNA mutagenesis, underscoring its versatility and significance in various experimental setups.
● Avam® Klenow Fragment (3’→5′ exonuclease) enzyme (10,000 U)
● 10X VividBlue™ (1 X 1.5 mL)
● Purity: >99%
● Specific Activity: 10,000 U/mg
● Single-stranded Exonuclease: <10% released
● Double-stranded Exonuclease: <1% released
● Double-stranded Endonuclease: No conversion
● E. coli DNA Contamination: <10 copies
● UDG Activity: <20 U/mL
● DNA labeling
● dA-tailing and dT-tailing for next-generation sequencing adapter
ligation
● Dideoxy DNA sequencing
● cDNA second strand synthesis
● Generation of single-stranded DNA probes
● Site-directed DNA mutagenesis
The enzyme lacks proofreading activities, making it suitable for applications where 5′→3′ exonuclease activity is undesirable, while retaining robust DNA synthesis capabilities
Yes, the enzyme is a proven choice for DNA labeling applications due to its efficient DNA polymerization activity.
dA-tailing and di-tailing are essential steps in preparing DNA libraries for next-generation sequencing, and the Avam® Klenow Fragment (3′→5′ exonuclease) enzyme is commonly used for these applications.
Yes, the enzyme is widely used for site-directed DNA mutagenesis experiments, facilitating the introduction of specific mutations into DNA sequences.
Yes, when stored properly at recommended temperatures, the enzyme remains stable for extended periods, ensuring reliable performance in molecular biology experiments.
Quantity | 10000U |
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