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
Heat Inactivation
85°C,5 min
Unit Definition
1 unit (U) is defined as the amount of enzyme required toincorporate10 nmol ofdNTPs into acid-insoluble precipitate under the reaction conditions of 65°C for 30 minutes.
Product Applications
This product is suitable for variousisothermalamplificationreactions such as LAMP,CPA,RCA,etc.
lacking 5′-3′ exonuclease activity. The enzyme has stronger 5′-3′ DNA polymerase activity, strand displacementactivityanddUTPtolerance,whichismoresuitableforanti-pollutionisothermalamplification reactions, such as LAMP,CPA,etc.
CAT
Components Name
Size
8,000 U
40,000 U
NaM702001-A
Lolina?Bst Plus DNA Polymerase (40 U/μL)
200μL
1mL
NaM702001-B
10× Lolina?Bst Plus DNA Polymerase Buffer
1mL
3×1mL
NaM702001-C
100 mM MgSO4
1mL
3×1mL
Instructions
1.Reaction System
Components
Volume(μL)
Final Concentration
10x Reaction Buffer
2.5
1x
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 (1U/μl)(optional)
1
0.04 U
DNA
10 ng–1μg
-
10x Primers
2.5
-
Lolina?Bst Plus DNA Polymerase (40U/μl)
1
1.6 U/μl
ddH2O
to 25
[Note]:
a)The amountofLolina?Bst Plus DNAPolymerasecan beadjustedandoptimizedaccordingtodifferent experiments.
b)10× Reaction Buffer: 200 mM Tris-HCl, 500 mM KCl,100 mM (NH4)2SO4, 20 mM MgSO4,1% Tween-20, pH 8.8 @ 25°C.
c)The Mg2+concentration can beadjusted between4–10 mMaccordingtodifferentexperiments.