Prestained Protein Marker (Triple color, EDTA free, 10-250 kDa)
In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
Tyramide Signal Amplification (TSA)
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Phos Binding Reagent Acrylamide
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
Cell Counting Kit-8 (CCK-8)
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
SYBR Safe DNA Gel Stain
Safe and sensitive stain for visualization of DNA or RNA in agarose or acrylamide gels.
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
The Prestained Protein Marker (Triple color, EDTA free, 10-250 kDa) is a prestained mixture of ten recombinant proteins ranging from 10 kDa to 250 kDa. Three different chromophores are bound to the proteins, 9 bands with blue, one red band at 70 kDa and one green band at 25 kDa. The Prestained Protein Marker is designed for observing protein separation during SDS-PAGE electrophoresis, verification of western transfer efficiency on membranes, and identifying the size of proteins. It can also be used in fluorescent imaging of membranes.
Prestained Protein Marker with increased brightness provides robust visualization for western blotting workflow, identifying target proteins on the gel or membrane, monitoring gel electrophoresis and confirming transfer quality.
The buffer of the marker does not contain EDTA which means it can be used in Phosbind SDS-PAGE electrophoresis (Cat. No. F4002)
The recommended loading volume for 1mm mini-gel is 3-5 μl. Larger size gels require more volume.
Quality Control & MSDS
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Components and Storage
|Prestained Protein Marker (Triple color, EDTA free, 10-250 KDa)||250uL|
|Prestained Protein Marker (Triple color, EDTA free, 10-250 kDa)||2x250uL|
Keep at -20°C for long-term storage and at 4°C for short-term storage.
Ready to use formulation for direct loading. No additional loading buffer or heat incubation are required.
No detectable protease-contaminating activities in the recombinant protein mixture.
Suitable for all common transfer membranes (PVDF, nylon and nitrocellulose).