Technical Data
A1020
Agarose Low Melting
25g
50g
100g
250g
50g
100g
250g
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Technical Data |
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A1020 |
Agarose Low Melting |
25g 50g 100g 250g |
| BioSeparation? | Storage: RT/4°CShipping: RT |
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Suitable for protein and large DNA separations 1000bp. The low melting temperature allows for the recovery, without damage, of nucleic acids below their denaturing temperatures. The low melting point also ensures that the agarose will be in a liquid state where in-gel manipulations can be performed without prior purification of the DNA from the gel slice. Genetic tested for a wide array of molecular biology procedures ensuring high recovery of biologically active DNA, high cloning efficiency and consistent reproducibility. Applications: • Analytical DNA Gels 1,000bp • Blotting Assays (Southern, northern) • Restriction Enzyme Digestion • Ligation• DNA Labeling• Nick Translation • Random Priming• PCR• Tissue Culture • Viral Plaque • For use with all buffer systems Recommended Usage (TBE): Concentration Molecular Weight 1% 250-10,000bp 1.5% 150-2500bp EEO: 0.12 pH (1.5%, Gel): As Reported Melting Point (1.5%): 66°C Gel Point (1.5%): 24-28°C Gel Strength (1.5%): 500g/cm2 Sulfate: 0.1% Ash: 0.4% Clarity (1.5%): 40NTU RNase: None Detected DNase: None Detected DNA Fragment Analysis: To Pass Test Background Fluorescence: To Pass Test Storage and Stability: Store 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. CAS Number: 9012-36-6 |
Form: White, homogeeous free flowing powder 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. |
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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)
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