Supercoiled DNA Ladder

Catalog # Concentration Size List Price Quantity Your Price
N0472S 500 µg/ml 100 gel lanes $170.00
$153.00
Catalog # Size List Price Your Price
N0472S 100 gel lanes $170.00
$153.00
Catalog #
Qty:
 
*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca
  • Supercoiled molecular weight marker
  • Size range: 2 kb to 10 kb
  • Convenient reference band at 5 kb
  • Supplied with a vial of Gel Loading Dye, Purple (6x), no SDS (NEB #B7025)
  • Suitable for 100 gel lanes

 

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The Supercoiled DNA ladder contains 9 proprietary supercoiled plasmids, ranging in size from 2 to 10 kb, that are suitable for use as supercoiled molecular weight standards for agarose electrophoresis. The 5 kb plasmid has an increased intensity to serve as a reference band.

  • Recommended gel percentage range: 0.6-1%
  • Optimum separation on 0.8% 
  • Recommended migration conditions: no more than 5V/cm (distance between electrodes), for no more than 60 minutes

Comes supplied with 1 vial of Gel Loading Dye, Purple (6X), no SDS.

Reagents Supplied

The following reagents are supplied with this product:

NEB # Component Name Component # Stored at (°C) Amount Concentration
  Supercoiled DNA Ladder N0472SVIAL -20 1 x 0.1 ml 500 µg/ml
  Gel Loading Dye, Purple (6X), no SDS B7025SVIAL 25 1 x 1 ml 6 X

Properties & Usage

Bases

Fragment Mass (ng) bp
1 45 10000
2 45 8000
3 45 6000
4 136 5000
5 45 4000
6 45 3500
7 45 3000
8 45 2500
9 45 2017

Effective Size Range

2,017bp to 10,000bp

Storage Buffer

10 mM Tris-HCl
1 mM EDTA
pH 8 @ 25°C



Materials Sold Separately
Notes
  • This ladder may contain some traces of nicked DNA and dimers above the 10 kb plasmid. To minimize nicking of the supercoiled DNA, always use sterile pipette tips and avoid multiple freeze-thaw cycles. The migration of supercoiled plasmids in agarose gels can change depending on agarose concentration, buffer and electrophoresis conditions. Dilute in TE or other buffer of minimal ionic strength. DNA may denature if diluted in dH20.
  • The 9 proprietary plasmids are purified, phenol extracted and equilibrated to 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA.
  • Centrifuge briefly and mix gently before use. We recommend loading 0.5 µg (1 µl) of the Supercoiled DNA Ladder diluted in sample buffer. This ladder was not designed for precise quantification of DNA mass, but can be used for approximating the mass of DNA in comparably intense samples of similar size.
  • Storage: Dividing in several aliquots is recommended to avoid multiple freeze-thaw cycles.
References
  • Sambrook, J., Fritsch, E.F. and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press. (2nd ed.),
Quality Control Assay
Quality Control tests are performed on each new lot of NEB product to meet the specifications designated for it. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. Further information regarding NEB product quality can be found here.
Specifications
The Specification sheet is a document that includes the storage temperature, shelf life and the specifications designated for the product. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]
Certificate of Analysis
The Certificate of Analysis (COA) is a signed document that includes the storage temperature, expiration date and quality controls for an individual lot. The following file naming structure is used to name these document files: [Product Number]_[Size]_[Version]_[Lot Number]
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This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.

New England Biolabs (NEB) is committed to practicing ethical science – we believe it is our job as researchers to ask the important questions that when answered will help preserve our quality of life and the world that we live in. However, this research should always be done in safe and ethical manner. Learn more.

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