Hieff™ Super Bst DNA Polymerase(120 U/μL) _ 14411ES

YeasenSku: 14411ES03

Size: 6000 U
Pris:
Försäljningspris$105.00

Frakt beräknad i kassan

Stock:
I lager

Beskrivning

Hieff™ Super Bst DNA Polymerase is derived from Thermophilic Geobacillus sp. DNA Polymerase I and has been genetically engineered to eliminate its 5’→3’ exonuclease activity. This product exhibits strong 5’→3’ DNA polymerase activity, strand-displacement activity, and tolerance to dUTP, making it particularly suitable for contamination-controlled isothermal amplification reactions such as LAMP and CPA. Compared to Bst Plus DNA Polymerase, Hieff™ Super Bst DNA Polymerase demonstrates enhanced thermostability, which improves amplification performance. The enzyme is well-suited for low-template-concentration assays and high-temperature LAMP reactions (e.g., at 70°C), effectively enhancing detection specificity and shortening time-to-result. Its thermostable nature also enables the development of hot-start Bst formulations for further improvement in assay specificity.

Specifications

Cat NO.

14411ES03 / 14411ES05 / 14411ES08

Size

6,000 U / 24,000 U / 120,000 U

Components

Components No.

Name

14411ES03

(6000 U)

14411ES05

(24000 U)

14411ES08

(120000 U)

14411-A

Hieff™ Super Bst DNA Polymerase(120 U/μL)

50 μL

200 μL

1 mL

14411-B

10× Hieff™ Super Bst DNA Polymerase Buffer

1 mL

1 mL

3 × 1 mL

14411-C

100 mM MgSO4

1 mL

1 mL

3 × 1 mL

Applications

This product is suitable for various isothermal amplification methods, including LAMP, CPA, and RCA. It supports LAMP reactions at 70°C or, when combined with a thermostable reverse transcriptase, enables RT-LAMP at 70°C.

Unit Definition

One unit (U) is defined as the amount of enzyme that incorporates 10 nmol of dNTPs into acid-insoluble material in 30 minutes at 65°C.

Enzyme Storage Buffer Composition

10 mM Tris-HCl, 50 mM KCl, 0.1 mM EDTA, 1 mM DTT, 0.1% Triton X-100, 50% glycerol, pH 7.5 @ 25°C.

Storage

Store at –25 to –15°C for 2 years. Avoid repeated freeze-thaw cycles.

Notes

1. Keep the enzyme on ice or in an ice bath during use, and return it immediately to –20°C after use.

2. This product is for research use only.

3. For your safety and health, wear a lab coat and disposable gloves during handling.

LAMP Experimental Example

1. Reaction Setup

Component

Volume (μL)

Final Concentration

10× Hieff™ Super Bst DNA Polymerase Buffer

2.5

100 mM MgSO₄

0.75

3 mM + 2 mM in buffer = 5 mM

dNTP Mix (25 mM each)

1.4

1.4 mM each

dUTP (25 mM) (optional)

1.4

1.4 mM

UDGase (1 U/μL) (optional)

1

0.04 U

Template DNA

10 ng–1 μg

10× Primers

2.5

Hieff™ Super Bst DNA Polymerase (120 U/μL)

0.34–1*

ddH₂O

to 25

[Note]: The amount of Hieff™ Super Bst DNA Polymerase may be optimized according to specific experimental requirements.

10× Buffer composition: 200 mM Tris-HCl, 500 mM KCl, 100 mM (NH₄)₂SO₄, 20 mM MgSO₄, 1% Tween-20, pH 8.8 @ 25°C.

Mg²⁺ concentration can be adjusted between 4–10 mM depending on the assay.

10× Primers: 16 µM FIP/BIP, 2 µM F3/B3, 4 µM Loop F/B each.

Our dNTP (Cat#10124), dUTP (Cat#10128), and UDGase (Cat#10303) are compatible with this product.

2. Reaction Conditions

Temperature

Time

Purpose

25–37°C

5–10 min

Degradation of uracil-containing templates (optional)

65–70°C

30–60 min

Amplification

85°C

5 min

Enzyme inactivation

Documents:

Safety Data Sheet

14411_MSDS_HB251205_EN.PDF

Manuals

14411_Manual_Ver.EN20251203.pdf

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