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peqGOLD Protein-Marker X Rabbit - Peqlab

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Data sheet<br />

<strong>peqGOLD</strong> <strong>Protein</strong> <strong>Marker</strong> X <strong>Rabbit</strong><br />

Lot No.<br />

________<br />

Usage Standard gel application 5 – 10 μl/lane<br />

Cat. No. 27-2710 1 x 250 μl<br />

27-2711 5 x 250 μl<br />

Description<br />

The <strong>peqGOLD</strong> <strong>Protein</strong> <strong>Marker</strong> X <strong>Rabbit</strong> is a mixture of 8 recombinant and highly purified proteins.<br />

Each protein contains an IgG-binding site and is proportioned to yield comparable gel electrophoresis<br />

and Western blotting band intensities. The ladder also contains a pink tracking dye in the buffer for<br />

monitoring electrophoresis and transfer in Western blotting. This formulation is appropriate for use<br />

with most rabbit and other non-mouse polyclonal antibodies.<br />

The marker can be detected using chemiluminescence, fluorescence, chromogenic or other detection<br />

systems.<br />

8 fragments 20, 30, 40, 50, 60, 80, 100 and 150 kDa<br />

Note<br />

All proteins resolve into clearly defined, sharp bands in the range of 20 kDa to 150 kDa when<br />

analysed by SDS-PAGE, and can be visualized by Coomassie Brilliant Blue R250 staining.<br />

As each protein contains an IgG-binding site protein bands can be detected in Western blotting by<br />

specific monoclonal antibodies followed by HRP-conjugated secondary antibody.<br />

Application<br />

Denaturing Polyacrylamide gels (SDS-PAGE)<br />

• Thaw marker at room temperature or heat at 37 – 40 °C for a few minutes.<br />

• Do not boil!<br />

• Vortex gently and apply 1 – 10 μl marker directly to the gel. Start the gel run.<br />

• Stop electrophoresis when the pink dye front has reached the bottom of the gel.<br />

• After electrophoresis visualize proteins by Coomassie staining or Western Blot detection.<br />

• Suggested loading volumes for various detection methods are shown in the following table:<br />

Detection system<br />

Loading volume (μl)<br />

Colorimetric 10<br />

Fluorescent 5 – 10<br />

Chemiluminescence 1 – 10<br />

ECL Substrate 5 – 10<br />

Super Signal West Pico Substrate 5 – 10<br />

Super Signal West Dura Substrate 2 – 5<br />

Super Signal West Femto Substrate 1 – 5<br />

PEQLAB_v0314_E<br />

info@peqlab.com · www.peqlab.com


<strong>peqGOLD</strong> <strong>Protein</strong> <strong>Marker</strong> X <strong>Rabbit</strong><br />

Note<br />

The marker was optimized for staining using Coomassie<br />

Brilliant Blue R-250, but can also be visualized by other<br />

staining methods (e.g. silver staining). As this method is<br />

10 to 100fold more sensitive than Coomassie staining, the<br />

amount of applied marker should be reduced accordingly.<br />

<strong>peqGOLD</strong> <strong>Protein</strong> <strong>Marker</strong> X contains SDS and is therefore<br />

not recommended to be used in native polyacrylamide gels<br />

for determing native molecular weights of proteins.<br />

If the marker shall be diluted use reducing loading buffer.<br />

Chemiluminescent detection of <strong>Protein</strong> <strong>Marker</strong> X <strong>Rabbit</strong>:<br />

The marker was separated by electrophoresis and transferred<br />

to a nitrocellulose membrane. <strong>Protein</strong>s were detected by<br />

hybridization with monoclonal rabbit antibodies followed by<br />

HRP-conjugated donkey-anti-rabbit secondary IgG, using ECL<br />

Western Blotting substrate.<br />

• Shipment: Blue ice<br />

• Storage: –20 °C<br />

• Stability: __________<br />

PEQLAB_v0314_E<br />

info@peqlab.com · www.peqlab.com

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