Enzymy

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

Fast and simple fragmentation

Fragment size easily controlled by incubation time

Ideal for NGS library preparation

High efficiency

Low GC bias

Input DNA: 500 pg to 1 µg

Fast and easy ligation

High efficiency

Optimized formulation

Highly active

Ready to use

Free of contamination

Rapid and efficient lysis

Ready-to-use 20 mg/ml solution

High thermal stability

High purity

Rapid and efficient RNA removal

Stable

Ready-to-use

Fast and easy ligation

Versatile use

Ready-to-use

Fast and easy ligation

Suitable even for challenging ligations

Ready-to-use

Fast and easy ligation

Suitable even for challenging ligations

ATP-dependent 3′ to 5′ helicase

expressed in E. coli

LbCas12a (D832A, with an Asp832→Ala substitution)

Origin: Lachnospiraceae bacterium (strain ND2006)

Purity > 95%

PFS 5′-GAAAG-3′

Origin: Sulfuricurvum sp. PC08-66

Purity > 95%

origin: E. coli carrying the Tn5 gene
random transposon insertion into DNA
requires 19-bp ME sequence

• hydrolyzes the phosphodiester backbone at the 5' end of the AP site
• creates a gap

• • activity at 45 °C to 70 °C
    purified from E. coli

synthesis at higher temperatures

reduced RNase H activity

easy to use

accuracy, yield, and sensitivity

high throughput

maximum sample volume

addition of deoxynucleotides to the 3′ hydroxyl terminus

origin: E.coli (gen from Z. albicollis)

purity > 95 %