Key Documents
Safety Information
P2192
10X PCR Buffer
Optimized for routine PCR with MgCl2 included
Synonym(s):
PCR Buffer Solution, PCR Reaction Buffer
Select a Size
CN¥669.75
Estimated to ship onJuly 02, 2025Details
Select a Size
About This Item
CN¥669.75
Estimated to ship onJuly 02, 2025Details
Recommended Products
Quality Level
form
liquid
packaging
vial of 1.5 mL
color
colorless
application(s)
agriculture
foreign activity
DNase, RNase, none detected
storage temp.
−20°C
Related Categories
1 of 4
This Item | 1710061 | 1710098 | 1710044 |
---|---|---|---|
species reactivity human, mouse | species reactivity human, Xenopus | species reactivity human, zebrafish, mouse, Xenopus, chicken, fish | species reactivity human |
clone monoclonal | clone monoclonal | clone monoclonal | clone 1.2.1.5.4, monoclonal |
shipped in dry ice | shipped in dry ice | shipped in dry ice | shipped in dry ice |
technique(s) ChIP: suitable, immunoprecipitation (IP): suitable, dot blot: suitable, western blot: suitable | technique(s) ChIP: suitable (ChIP-seq), immunoprecipitation (IP): suitable | technique(s) ChIP: suitable, immunoprecipitation (IP): suitable, western blot: suitable | technique(s) ChIP: suitable, ELISA: suitable, dot blot: suitable, immunohistochemistry: suitable, immunoprecipitation (IP): suitable, multiplexing: suitable, western blot: suitable |
Gene Information human ... TCF7L2(6934) | Gene Information - | Gene Information human ... TBP(6908) | Gene Information human ... CTCF(10664) |
Application
Features and Benefits
- Standalone buffer
- Compatible with JumpStart™ Taq DNA Polymerase (D9307), Taq DNA Polymerase from Thermus aquaticus (D1806), and REDTaq® Genomic DNA Polymerase (D8312)
Components
Legal Information
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Regulatory Information
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Protocols
Protocol using antibody mediated hot start polymerase with a red dye for easy gel loading. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.
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