Hieff Unicon™ Hotstart Direct Taq DNA Polymerase, Glycerol-free, 40 U/μL _ 14322ES yeasen
$300.00
In stock
SKU
14322ES76
Product Description
Hieff Unicon™ Hotstart Direct Taq DNA Polymerase is a hot start DNA polymerase that is resistant to blood and other inhibitors. The product is blocked by antibodies and has good amplification sensitivity and specificity. After heating for 30 seconds at the pre-denaturation temperature, the antibody is completely inactivated and the DNA polymerase activity is released. The amplification induced by nonspecific annealing of primers could be effectively inhibited by using the hot start Taq enzyme. Th e Taq DNA Polymerase is Glycerol-free and can be used for the formulation of lyophilized reagents. Components.
Product Information
- Components No.
- Name
- 14322
- ES
- 76
- (
- 2 K
- U
- )
- 14322
- ES
- 80
- (
- 7 KU
- )
- 14322
- ES
- 92
- (
- 20 KU
- )
- 14322
- ES
- 93
- (
- 50 KU
- )
- 14322
- ES
- 95
- (
- 100 KU
- )
- 14322
- Hotstart D-Taq
- , Glycerol-free
- (
- 40
- U/
- μL
- )
- 5
- 0 μL
- 175
- μL
- 500
- μL
- 1.25
- mL
- 2.5
- mL
Storage
The product should be stored at 2 ~ 8 ℃ for 1 years.
Instructions
1. Reaction Composition
Components
- Volume (μL)
- Final Concentration
- 2
- ×Buffer
- a
- 12.5
- 1×
- Primer
- Probe Mix
- b
- X
- 0.1 -0.5 μM
- Hotstart D-Taq
- , Glycerol-free
- (
- 40
- U/
- μL
- )
- c
- 0.175
- 0.
- 28
- U/μL
- Template DNA
- b
- X
- 0.1-100 ng
- ddH
- 2
- O
- to 25
Notes
Be sure to mix well before use, avoid excessive bubbles caused by violent vibration. a) According to the specific experimental application, it is needed to prepare the corresponding reaction buffer. If a basic buffer (10×) is required, Cat#11374 is recommended. b) The amount of DNA and the concentration of probes or primers are recommended concentrations. The optimal concentration can be adjusted according to the specific experimental conditions. c) The amount of enzyme can be adjusted according to the experimental application. 2. Optimized Cycling Protocol Reaction stage Temperature Time Cycle 1 Initial denaturation 95°C 5 min 1 2 Amplification reaction 95°C 15 sec 45 cycles 60°C a 30 sec b a) Amplification reaction: The temperature is adjusted according to the Tm value of the designed primers. b) Fluorescence signal acquisition: Please set the experimental procedure according to the requirements of the instrument manual.
1. This product is for research use only. 2. Please operate with lab coats and disposable gloves for your safety.
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