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TriDye™ 2-Log DNA Ladder (0.1 - 10.0 kb)
Quick-Load® 2-Log DNA Ladder(0.1-10.0 kb)
Catalog # Size Concentration Price Qty  
N0469S 125 gel lanes 100 μg/ml $79.00
Prices are in US dollars and valid only for US orders.
Download:Technical Bulletin|MSDS PDF


Description:
Quick-Load® 2-Log DNA Ladder is a pre-mixed, ready-to-load molecular weight marker containing bromophenol blue as a tracking dye.

The DNA Ladder consists of proprietary plasmids which are digested to completion with appropriate restriction enzymes to yield 19 bands suitable for use as molecular weight standards for agarose gel electrophoresis. This digested DNA includes fragments ranging from 100 bp to 10 kb. The 0.5, 1.0 and 3.0 kb bands have increased intensity to serve as reference bands.





Quick-Load 2-Log DNA Ladder visualized by ethidium bromide staining on a 1.0% TBE agarose gel. Mass values are for 1 µg/lane.



Effective Size Range: 100 bp to 10 kb

Source:
The double-stranded DNA is digested to completion with appropriate restriction enzymes, phenol extracted and equilibrated to 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA.

FragmentSize (bp)Mass (ng)
110,00240
28,00140
36,00148
45,00140
54,00132
63,001120
72,01740
81,51757
91,20045
101,000122
1190034
1280031
1370027
1460023
15a517124
15b500124
1640049
1730037
1820032
1910061

Concentration:
100 μg/ml

Recommended Load: 1 μg


Storage Conditions


Storage Conditions:
3.3 mM Tris-HCl
11 mM EDTA
0.015% Bromophenol Blue
0.017% SDS
2.5% Ficoll 400
pH 8.0 @ 25°C

Storage Temperature:
4°C


Notes


General notes:
  1. Quick-Load 2-Log DNA Ladder is stable for at least 6 months at 25°C.
  2. For long term storage, store at 4°C or -20°C. If stored at -20°C, mix well after thawing.
Usage notes:
  1. Preparation of DNA: The double-stranded DNA is digested to completion with appropriate restriction enzymes, phenol extracted and equilibrated in storage buffer.
  2. We recommend loading 10 μl (1.0 μg) or Quick-Load 2-Log DNA Ladder per gel lane.
  3. The Quick-Load 2-Log DNA Ladder is not intended for precise quantification of DNA mass but can be used for approximating the mass of DNA in comparably intense samples of similar size.

FAQs


  1. What are the overhangs on the DNA ladder fragments? Can I end-label them using the T4 polynucleotide kinase (PNK)? What about the Klenow fragment?
  2. Why are the DNA ladders showing up on my Southern blot? What is the sequence or composition of the ladder bands?
  3. How can I quantify the amount of DNA in each band of a marker?

References


  1. Sambrook, J., Fritsch, E. F. and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, (2nd ed.), Cold Spring Harbor: Cold Spring Harbor Laboratory Press, 10.51-10.67.


Companion Products


1 kb DNA Ladder
100 bp DNA Ladder
2-Log DNA Ladder (0.1–10.0 kb)
Quick-Load® 1 kb DNA Ladder
Quick-Load® 100 bp DNA Ladder
TriDye™ 1 kb DNA Ladder
TriDye™ 100 bp DNA Ladder
TriDye™ 2-Log DNA Ladder (0.1 - 10.0 kb)

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