Agarose DNA Fragments 50-2000bp (3:1 Blend)
|BioSeparation?||Storage: RTShipping: RT|
Agarose for DNA Fragments 50-2000bp is manufactured from selected algae and harvested during specific periods of growth to produce gels that are easier to prepare than the equivalent polyacrylamide gels.
Manufactured specifically for primer size fragments in the range of 50-2000 base pairs and exhibits exceptionally high transparency even at high concentrations (5%).
Specially purified to be free of background contamination that could interfere with restriction digests or ligations and selected for use in PCR product analysis.
• Analytical DNA Gels 2000bp
• PCR products
• Restriction Enzyme digestion products
• Capillary Electrophoresis
• Mutation Analysis
• For use with all buffer systems
Recommended Usage (1X TAE):
Concentration Molecular Weight
Note: A 3% agarose gel is equivalent to 8% polyacrylamide
Storage and Stability: Store powdered agarose at RT. Opened bottles should be capped tightly and kept in a low humidity environment. For greater separation capacity, keep the gel at 4°C for 1 hour before use.
White. granular, free flowing powder
Gel Strength (1.5%):
Gel Strength (4%):
pH in Solution (1.5%,H2O):
Loss on Drying:
To Pass Test
Background Fluorescence (EtBr):
To Pass Test
Quality Control: Genetic tested for a wide array of molecular biology procedures ensuring high recovery of biologically active DNA, high cloning efficiency and consistent reproducibility.
Functional and Molecular Biology Testing: To Pass Test
• Comparative assay of different size DNA fragments
• Southern Blot (125-23,000bp)
• Background Fluorescence (TAE/TE, EtBr):
• DNA Binding (TAE, EtBr)
• Restriction Ligation Assay (Bam HI, Hinc II, EcoR I, Hind III, Pst I, and T4 DNA Ligase)
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
1. Ausubel, F.M., et al., Current Protocols in Molecular Biology, John Wiley (1992). 2. Maniatis, T., et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press (1989).