Hieff™ UltraShear Methylated DNA Fragmentase _ 12218ES

Yeasen제품번호: 12218ES08

Size: 8 T
가격:
판매 가격$55.00

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설명

Hieff™ UltraShear Methylated DNA Fragmentase is an optimized enzyme mixture specifically designed for DNA fragmentation prior to library preparation. Unlike conventional fragmentation enzymes, this formulation preserves DNA methylation marks. Compared to traditional sonication, this product causes minimal damage to DNA templates, results in lower sample loss, and eliminates the cumbersome sonication step—making the fragmentation process simpler and more efficient. It is suitable for 5–250 ng of standard genomic DNA from animals, plants, or microorganisms, and is also compatible with FFPE-derived DNA.

Features

Methylation-Friendly: Preserves methylation marks and is fully compatible with methylation library preparation.

Gentle and Efficient: Minimizes template damage and sample loss while enabling one-step fragmentation.

Broad Compatibility: Works with 5–250 ng DNA from plants, animals, microbes, and FFPE samples; no sonication required and automation-friendly.

Components

Components No.

Name

12218ES08

(8 T)

12218ES24

(24 T)

12218ES96

(96 T)

12218-A

 

UltraShear Reaction Buffer

56 μL

168 μL

672 μL

12218-B

 

UltraShear Enzyme

48 μL

144 μL

576 μL

12218-C

 

UltraShear Reagent

8 μL

24 μL

96 μL

Storage

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

Application

dsDNA fragmentation; Methylation library preparation

Instructions

1. Thaw reagents listed in Table 1, invert to mix, and keep on ice.

2. Prepare the reaction mix for DNA fragmentation on ice as described in Table 1.

Table 1. DNA Fragmentation Reaction Setup

Component

Volume (μL)

Input DNA

X

UltraShear Reaction Buffer

7

UltraShear Enzyme

6

ddH₂O

Up to 60

3. Gently mix by pipetting or light vortexing, then briefly centrifuge to collect liquid at the bottom of the tube.

4. Place the PCR tube in a thermal cycler and run the program outlined in Table 2.

Table 2. DNA Fragmentation Thermal Cycling Program

Temperature

Time

Heated Lid

105°C (On)

4°C

1 min*

37°C

5–40 min**

65°C

20 min

4°C

Hold

[Note]:

*To precisely control fragmentation and avoid over-digestion, pre-cool the thermal cycler block to 4°C before loading samples.

**For intact genomic DNA, refer to Table 3 for recommended incubation times.

Table 3. Recommended Fragmentation Times for Intact Genomic DNA

Target Insert Size (Peak)

Fragmentation Time

2000 bp

5 min

1000 bp

10 min

600 bp

15 min

400 bp

20 min

250 bp

25 min

150 bp

30 min

[Note]: For fragmented or low-integrity FFPE DNA, a 5–15 minute incubation at 37°C is recommended; optimization may be required.

5. Purify the fragmented DNA using Hieff NGSTM DNA Selection Beads (Cat#12601), AMPure XP Beads (Cat#A63880), or equivalent products. Purified DNA can be stored at –20°C for downstream applications.

Documents:

Safety Data Sheet

12218_MSDS_HB251211_EN.PDF

Manuals

12218_Manual_Ver.EN20251211.pdf

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