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Peqlab peqGOLD, Protein Marker V (Pre-Stained)

Peqlab peqGOLD, Protein Marker V (Pre-Stained)

Supplier: VWR Chemicals

Protein Marker V (pre-stained) for monitoring protein separation, transfer efficiency and size determination.

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Peqlab peqGOLD, Protein Marker I (Unstained)

Peqlab peqGOLD, Protein Marker I (Unstained)

Supplier: VWR Chemicals

peqGOLD Protein Marker I is a mixture of seven purified proteins which are re-dissolved 'ready to use' in loading buffer. The proteins resolve into sharp, tight bands in the range of 14,4 to 116,0 kDa when analysed by SDS-PAGE and stained with Coomassie Brilliant Blue R-250.

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VWR®, Protein marker III (pre-stained), peqGOLD

VWR®, Protein marker III (pre-stained), peqGOLD

Supplier: VWR Chemicals

Protein Marker III for monitoring protein separation, transfer efficiency and size determination.

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Peqlab peqGOLD, Protein Marker II (Unstained)

Peqlab peqGOLD, Protein Marker II (Unstained)

Supplier: VWR Chemicals

Protein Marker II for accurate molecular weight determination of proteins by SDS-PAGE.

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VWR®, Protein marker VI (pre-stained), peqGOLD

VWR®, Protein marker VI (pre-stained), peqGOLD

Supplier: VWR Chemicals

peqGOLD pre-stained Protein Marker VI is a mixture of 10 coloured proteins. These proteins are recombinantly produced in E.coli, highly purified and supplied 'ready to use' in loading buffer. The protein concentrations are optimised to yield well-defined bands directly visible in SDS polyacrylamide gels.

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Peqlab peqGOLD, Protein Marker IV (Pre-Stained)

Peqlab peqGOLD, Protein Marker IV (Pre-Stained)

Supplier: VWR Chemicals

peqGOLD pre-stained protein marker IV is a mixture of 10 recombinant, highly purified coloured proteins supplied 'ready to use' in loading buffer. The protein concentrations are optimised to yield well-defined bands directly visible in SDS-polyacrylamide gels.

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VWR®, Nucleic acid loading dyes

VWR®, Nucleic acid loading dyes

Supplier: VWR Chemicals

Designed to optimise loading nucleic acids in agarose gels, the loading dye imparts colour to the sample to facilitate the loading process and increase the density of the sample to ensure efficient sample distribution into each well. The dye migrates independently from the sample, allowing estimation of the migration of nucleic acids.

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