Features: Supplied in 6X Loading buffer
The BstII digest of phage-DNA yields the 14 fragments. Lambda DNA was completely digested by BstII, phenol extracted,
ethanol precipitated, dissolved in 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA. The marker is ready-to-use.
Usage: 0,5 µg/lane
Concentration: 0,2 µg/µl
Number of bands: 14 8453*, 7242, 6369, 5687*, 4822, 4324, 3675, 2323, 1929, 1371, 1264, 702, 224, 117
Agarose Gel / Polyacrylamide Gel
- Vortex gently before using
- apply 0,5 µg (agarose) or 0.5-0.9 µg (polyacrylamide gel) per 1 mm lane
See the graph for the percentage of the bands per band in ng, relating to 0.5 μg loaded marker. Use the same volume of DNA and marker. Additionally the
concentration of loading buffer in samples and marker should be equal.
Dilute in TE or other buffer of minimal ionic strength. DNA may denature if diluted in dH2O and subsequently heated.
*The cohesive ends (12b cos site of bacteriophage) of fragments 8453 bp and 5687 bp may anneal to and form the additional band. These fragments may be separated by heating to 65°C for 5 min and
then cooling on ice for 3 min.
Transportation: Shipped on blue ice or room temperature
Storage: at -20°C for 24 months