Protein Marker US7
Protein Molecular Weight Marker US7 (unstained) is ideal for precise sizing of proteins by SDS-PAGE
| Cat.-no |
Description |
Amount |
Price € |
Shop |
| 310001 |
Protein Marker US7 (14.4 - 116 kDa) * |
2 x 1 ml |
45.00 |
add |
| 310002 |
Protein Marker US7 (14.4 - 116 kDa) |
5 x 1 ml |
109.00 |
add |
* up to 400 mini gels or 200 standard gels
Protein Marker: Order by E-mail
Protein Marker: Datasheet
Protein Marker: Deutsche Beschreibung
Description/Preparation:
The Protein Marker US7 is a mixture of 7 purified proteins which are re-dissolved 'ready-to-use' in loading buffer. The proteins resolve into 7 sharp bands in the range of 14.4 kDa to 116.0 kDa when analyzed by SDS-PAGE and stained with optimized dye.
Usage:
Mini gel application: 5 – 10 μl/well
Standard gel application: 10 – 20 μl/well
Storage Buffer/Tracking Dye:
62.5 mM Tris-HCl (pH 7.0, 25 °C), 1 mM EDTA, 2 % SDS, 50 mM DTT, 30 mM NaCl, 1 mM NaN3, 0.01 % bromophenol blue and 50 % glycerol
Concentration:
0.1 - 0.2 mg/ml each protein
Number of bands: 7 14.4, 18.4, 25.0, 35.0, 45.0, 66.2, 116.0 kDa
Loading:
Loading Denaturing Polyacrylamide gels (SDS-PAGE):
- Thaw marker at room temperature or heat at 37 – 40 °C for a
few minutes.
- Vortex gently.
- Take the required amount of marker from the stock solution and
transfer to a clean tube.
- Heat this aliquot to 95 °C for 5 minutes for complete denaturation
of the proteins. Cooled and mixed solution is ready for loading on
an SDS-PAGE.
- Store denatured marker at – 20 °C. For further loading only thaw
again at room temperature or heat at 37 – 40 °C. Vortex gently
and apply to the gel.
- 2 ml marker are sufficient for 400 mini gels or 200 standard gels.
It is recommended to divide the marker into aliquots to avoid contamination of the stock solution.
Recommended loading volumes
Mini Gel: 5 µl/0.75 mm; 10 µl/1.5 mm
Standard Gel: 10 µl/0.75 mm; 20 µl/1.5 mm
Note:
Protein Marker US7 is optimized for runs on 12 % SDS polyacrylamide gels. 8 to 10 % gels may cause
proteins with low molecular weights to migrate with the dye front. On 12 to 15 % and gradient gels all bands are visible.
The marker is optimized for use with Coomassie Brilliant Blue R-250, but can also be used with other gel staining methods (e.g. silver staining etc.). As this method is 10 to 100 times more sensitive than Coomassie Blue staining the amount of marker applied should be decreased accordingly.
Protein Marker US7 contains 2 % SDS and is therefore not recommended to be used in native polyacrylamide gels for determing native molecular weights of proteins.
Storage: at -20°C
Shipment: on blue ice
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