B4930
Capillary Electrophoresis Running Buffer (10x)
for automated DNA sequencing
Synonym(s):
Running Buffer, Sequencing Buffer
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About This Item
UNSPSC Code:
12352200
NACRES:
NA.25
Recommended Products
grade
for molecular biology
Quality Level
type
for automated DNA sequencing
form
liquid
technique(s)
DNA sequencing: suitable
storage temp.
room temp
Related Categories
Application
Capillary Electrophoresis Running Buffer (10x) has been used for automated sequencing by capillary electrophoresis.
Features and Benefits
- Compatible with ABI Prism 3700 DNA Analyzer and Molecular Dynamics MegaBACE capillary electrophoresis instruments
- Provides consistency and high performance for every batch
- Stable at room temperature for convenient shipping, and storage
- Tested and works well with the performance-optimized polymer 6 (POP6)
- Cost-efficient - high-quality buffer at a great value
- Quality control testing of every lot ensures proper pH, conductivity, and performance for Capillary Electrophoresis Sequencing
- Plastic bottles provide easy handling
- Available in one, four and 20 L as well as custom packaging options available
Preparation Note
Product should be diluted to 1x before use. Add 1 volume of the 10X capillary electrophoresis buffer solution to 9 volumes of deionized water. Cover the top of the container and mix the 1X solution by inversion.
Other Notes
Capillary Electrophoresis Buffer is for laboratory use only. Not for drug, household, or other uses.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Wolf-Matthias Leeder et al.
Bio-protocol, 11(5), e3935-e3935 (2021-04-03)
Gene expression within the mitochondria of African trypanosomes and other protozoan organisms relies on a nucleotide-specific RNA-editing reaction. In the process exclusively uridine (U)-nucleotides are site-specifically inserted into and deleted from sequence-deficient primary transcripts to convert them into translatable mRNAs.
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