Hieff™ Bst Plus DNA Polymerase (2000 U/μL)

Details:

Product Description

Hieff Bst Plus DNA Polymerase is derived from Thermophilic Geobacillus sp DNA Polymerase I, lacking 5'-3' exonuclease activity. The enzyme has stronger 5'-3' DNA polymerase activity, strand displacement activity and dUTP tolerance, which is more suitable for anti-pollution isothermal amplification reactions, such as LAMP, CPA, etc.

Product Components

Component number

Components

Cat#/Size

14403ES20 (20,000 U)

14403ES70 (200,000 U)

14403ES84 (2,000,000 U)

14403ES10 (10 mL)

14403ES72 (200 mL)

14403

Hieff™ Bst Plus DNA Polymerase (2,000 U/μL)

10 μL

100 μL

1 mL

2× 5 mL

40× 5 mL

Applications

Suitable for a variety of isothermal amplification reactions such as LAMP, CPA, RCA, etc.

Activity Definition

1 U refers to the amount of enzyme required to incorporate 10 nmol of dNTP into the acid-insoluble precipitate in 30 min at 65°C.

Preservation Solution Components

10 mmol/L Tris-HCl, 50 mmol/L KCl, 0.1 mmol/L EDTA, 1 mmol/L DTT, 0.1% Triton X-100, 50% Glycerol, pH 7.5 @ 25℃.

Heat Inactivation

Incubation at 85°C for 5 min.

Shipping and Storage

The product is shipped with ice pack and can be stored at -20°C for 2 years. Please avoid repeated freeze-thaw.

Cautions

1. Enzymes should be stored in an ice box or on an ice bath when used, and should be stored at -20°C immediately after use.
2. For your safety and health, please wear lab coats and disposable gloves for operation.
3. This product is for research use ONLY!

Protocol for LAMP

1. Recommended reaction system

Components

Volume (μL)

Final Concentration

10×Reaction Buffer

2.5

100 mmol/L MgSO4

0.75

3 mmol/L+2 mmol/L in buffer= 5 mmol/L

dNTP Mix (25 mmol/L each)

1.4

1.4 mmol/L each

dUTP (25 mmol/L) (optional)

1.4

1.4 mmol/L

UDGase (1 U/μL) (optional)

1

0.04 U

DNA

10 ng~1 μg

-

10×Primers 

2.5

-

HieffTM Bst Plus DNA Polymerase (2,000 U/μL)

1*

1.6 U/μL

ddH2O

to 25

-

Note: 1. *: According to different experiments, the concentration of HieffTM Bst Plus DNA Polymerase can be adjusted and optimized;
2. 10×Reaction Buffer: 200 mmol/L Tris-HCl, 500 mmol/L KCl, 100 mmol/L (NH4)2S04, 20 mmol/L MgS04, 1% Tween-20, pH 8.8 @ 25℃.
3. If optimization is desired, try titrating concentration of Mg2+ (4–10 mmol/L final).
4. 10× Primers: 16 µmol/L FIP/BIP, 2 µmol/L F3/B3, 4 µmol/L Loop F/B each.
5. Yeasen Biotech products: dNTP (Cat#10124), dUTP (Cat#10128) and UDGase (Cat#10303) can be used with this product. 

2. Reaction conditions

Temperature

Time

Effect

25~37°C

5~10 min

Degradation of U-containing templates (optional)

65°C

30~60 min

Reaction

85℃

5 min

Deactivation

COA Please fill out the COA application form

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