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FAQs for λ DNA-Mono Cut Mix
Protocols for λ DNA-Mono Cut Mix
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Reagents Sold Separately
Gel Loading Dye, Blue (6X)
Companion Products
1 kb DNA Ladder
100 bp DNA Ladder
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PCR Marker
TriDye™ 1 kb DNA Ladder
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λ DNA-Mono Cut Mix
Catalog # Size Concentration Price Qty  
N3019L 500 gel lanes 500 μg/ml $244.00
N3019S 100 gel lanes 500 μg/ml $61.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Description:
The Mono Cut Mix is a mixture of intact lambda DNA and lambda DNA separately digested with ApaI, KpnI, XbaI and XhoI. The fragments have been filled in with DNA Polymerase I Large (Klenow) Fragment to prevent re-annealing. These fragments are best separated by Pulsed Field Gel Electrophoresis.The approximate mass of DNA in each of the bands is provided (assuming a 0.5 μg load) for approximating the mass of DNA in comparably intense samples of similar size.





PFGE separation of 0.5 µg of Lambda Mono Cut Mix. 1% agarose gel, 0.5X TBE, 6 V/cm, 15°C for 20 hours. Switch times ramped from 0.5-1.5 seconds.



Effective Size Range: 1,503 bp to 48,502 bp

Source:
The phage is isolated from the heat- inducible lysogen E. coli λ c1857 S7 and then isolated from the purified phage by phenol extraction and dialyzed. The double-stranded DNA is then digested to completion with the appropriate enzyme, phenol extracted and dialyzed against 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA.


Reagents Supplied:
Gel Loading Dye, Blue (6X)

FragmentSize (bp)Mass (ng)
148,502100
238,41679
333,49869
429,94662
524,50851
623,99449
717,05335
815,00431
910,08621
101,5033

Concentration:
500 μg/ml

Recommended Load: 0.5 μg


Storage Conditions


Storage Conditions:
10 mM Tris-HCl
1 mM EDTA
pH 8.0 @ 25°C

Storage Temperature:
-20°C


Notes


Usage notes:
  1. These fragments are best separated by Pulsed Field Gel Electrophoresis. Alternatively Lambda Mono Cut Mix can be separated by conventional gel electrophoresis using the following conditions: 0.5 μg Lambda Mono Cut Mix, 0.4 % agarose gel, 1X TAE, 10 V, 25°C for 24 hours.
  2. 1X Gel Loading Dye, Blue:
    2.5% Ficoll-400
    11 mMEDTA
    3.3 mM Tris-HCL (pH 8.0@25°C)
    0.017% SDS
    0.015% bromophenol blue

FAQs


  1. How can I quantify the amount of DNA in each band of a marker?
  2. General information on Lambda DNA Mono Cut Mix:

Protocols
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Protocols for λ DNA-Mono Cut Mix


References


  1. Daniels, D.L. et al. (1983) In Appendix II: Complete Annotated Lambda Sequence. R.W. Hendrix, J.W. Roberts, F.W. Stahl and R.A. Weisberg (Eds.), Lambda-II, pp. 519-676. 


Reagents Sold Separately


Gel Loading Dye, Blue (6X)


Companion Products


1 kb DNA Ladder
100 bp DNA Ladder
2-Log DNA Ladder (0.1–10.0 kb)
PCR Marker
TriDye™ 1 kb DNA Ladder
TriDye™ 100 bp DNA Ladder
TriDye™ 2-Log DNA Ladder (0.1 - 10.0 kb)

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