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C A T A L O G
 

Prestained Protein Molecular Weight Marker

 

Lot specific pictures:
21726, 23251, 24549,
26792

#SM0441  2x250 µl
(for 100 mini gel applications, 5 µl/well
or 50 large gel applications, 10 µl/well)

Related Documents (in pdf, ~100 KB):

Certificate of Analysis: #SM0441
MSDS (English)
MSDS (English-USA)
MSDS (German)
LabAid™

 

Features

Description
The Prestained Protein Molecular Weight Marker is designed for monitoring protein separation during SDS-polyacrylamide gel electrophoresis (1), verification of Western transfer efficiency and approximate sizing of proteins. The marker is a mixture of 6 proteins with the apparent molecular weights from 20 kDa to 120 kDa. All proteins of the marker are covalently coupled to a blue chromophore.
The Prestained Protein Molecular Weight Marker can be used in Western blotting on PVDF, nylon and nitrocellulose membranes.

Applications

Composition
Approximately 0.2 mg/ml of each protein in 62.5  mM Tris-HCl (pH 7.5 at 25°C), 1  mM EDTA, 2% SDS, 10  mM DTT, 1.5  mM NaN3 and 33% glycerol.

Quality Control
Tested in SDS-polyacrylamide gel electrophoresis and Western blotting.

Storage
Store at -20°C.

Recommendations for Loading
  1. Thaw the marker either at room temperature or at 37-40°C for a few minutes to dissolve precipitated solids. Do not boil.
  2. Mix gently, but thoroughly, to ensure that the solution is homogeneous.
  3. Load the following volumes of the marker on SDS-polyacrylamide gel:
    - 5 µl per well for mini-gels, 3 µl per well for blots;
    - 10 µl per well for large gels, 6 µl per well for blots.

Note

  • The indicated loading volume is recommended for gels with a thickness of 0.75 mm. For thicker gels, the loading volume should be increased.
  • Each lot of Prestained Protein Molecular Weight Marker is calibrated against a precisely sized Unstained Protein Molecular Weight Marker in Tris-glycine gel and the calculated apparent molecular weights are reported in the product’s Certificate of Analysis.
  • Prestained proteins can have different mobilities in various SDS-PAGE-buffer systems. However, they are suitable for approximate molecular weight determination when calibrated against unstained standards in the same system.
  • A separation gel resolves proteins effectively according to their molecular weight. Linear gradient gels are used for resolution of both small and large proteins, while low percentage gels are recommended for analysis of large proteins. In these gels, small proteins migrate with the tracking dyes during electrophoresis.

 

Related Products

Reference

  1. Laemmli, U.K., Cleavage of structural proteins during the assembly of the head of bacteriophage T4, Nature, 227, 680-685, 1970.

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Updated vasario 06, 2008 16:37