Protein MW Marker, Ladder, Prestained, 10-170kD

Cat# P9106-51-250ul

Size : 250ul

Brand : US Biological

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P9106-51 Protein MW Marker, Ladder, Prestained, 10-170kD

Clone Type
Polyclonal
Applications
WB
Shipping Temp
Blue Ice
Storage Temp
4°C/-20°C

Prestained Protein Ladder, 10-170kD is a mixture of 10 recombinant, highly purified colored proteins, designed for monitoring of protein separation during SDS-PAGE, verifying Western transfer efficiency and approximating the molecular weight of blotted proteins. Proteins are covalently coupled with a blue chromophore except two reference one - ~70kD, (orange) and ~10kD (green). The Prestained Protein Ladder is supplied in gel loading buffer and is ready-to-use.||Note: 250ul is sufficient for 50 mini-gel applications (5ul/well) or 25 large gel applications (10ul/well)||5ul of Prestained Protein Ladder provide 10 bands of equal intensities in 4-20% SDS-PAGE (Tris-glycine buffer) and after electrotransfer onto PVDF membrane.||Applications:|Suitable for use in monitoring of protein separation during SDS-PAGE (1); Verifying Western transfer efficiency (2, 3); Approximating the molecular weight of blotted proteins.||Protocol:|1. Thaw Ladder at RT. Do not boil!|2. Mix gently, but thoroughly to ensure the solution is homogeneous.|3. Load the Ladder on a gel and run. (Load volume: 5ul for mini-gels, ; 10ul for large gels, use same volumes for blots).|4. After run is complete, stain gel or perform Western transfer procedure as desired.||Note: |• <10% gels may cause proteins with low molecular weights to migrate with the dye front.|• Loading volumes are intended for use in gels with a thickness of 0.75mm. If thicker gels are used, the loading voume should be increased.|• Prestained Protein Ladder could be used in Western Blot with all common membranes: PVDF, nylon and nitrocellulose.|• Longer transfer times or higer voltages may be required for Western Blot of large (>100kD) proteins.||Storage and Stability:|May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Applications
Form: Supplied as a liquid in 62.5mM Tris-H3PO4, pH 7.5, 1mM EDTA, 2% SDS, 10mM DTT, 1mM sodium azide, 33% glycerol||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Form
Supplied as a liquid in 62.5mM Tris-H3PO4, pH 7.5, 1mM EDTA, 2% SDS, 10mM DTT, 1mM sodium azide, 33% glycerol
References
1. Laemmli, U.K., Cleavage of structural proteins during the assembly of the head of bacteriophage T4, Nature, 227, 680-685, 1970.|2. Burnette, W.N., "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate - polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A, Anal Biochem., 112 (2), 195-203, 1981.|3. Towbin, H., et al., Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications, Proc. Natl. Acad. Sci. USA, 76, 4350-4354, 1979.

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