Highly Competitive Performance - High Throughput, Excellent Sample Preservation Rate & Detection Sensitivity
5U/μL
Stored at: -20℃
REF GSP9161 Spec: 50μL(250U)
GSP9162 100μL(500U)
GSP9163 500μL(2500U)
GSP9164 1000μL(5000U)
Klenow Fragment is a mesophilic DNA polymerase derived from the E. coli Polymerase I. The enzyme exhibits DNA synthesis and proofreading (3′→5′) nuclease activities, and, in the absence of the holoenzyme’s (5′→3′) nuclease domain, displays a moderate strand displacement activity during DNA synthesis.
Simple and rapid isothermal reaction speeds up the preparation of plasmid samples for sequencing
High fidelity, strong chain switching activity, suitable for whole genome amplification
Cut off the 3 'protruding end or flatten the 5' protruding end to form a flat end
Preparation of probes or markers using random primers
Synthesis of double stranded DNA in oligonucleotide directed mutagenesis
Double deoxygenation method for DNA sequencing (Sanger method)
1. The enzyme synthesis activity is consistent with well-known domestic brands
Fig. DNA extends, fragment length increases, and Tm value increases
2. Excellent database connection performance after flat end construction
Fig. Plasma free DNA was subjected to flat end ligation and then a library was constructed
