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Protein labeling reagents are reactive dyes that attach to a specific functional group (i.e., amine or thiol) on a target biomolecule allowing for its subsequent detection or purification. Use the Protein Labeling Reagents Selection Tool to find the best reactive dye for your application or learn...
Use this interactive selection guide to find the right protein labeling reagent for your experiment. Step 1: Choose your options. Simply select the features you need from the options listed. As you define your parameters the list of available reagents matching your selection will appear in the panel...
Find a wide range of products for biotinylation, crosslinking, and modification of proteins, peptides, and antibodies. These bioconjugation reagents are commonly used to study the structure and interaction of proteins, build immunoassays, increase protein solubility, or attach molecules to surfaces.
Total protein normalization is a useful method for obtaining accurate, quantitative western blotting data. The Invitrogen No-Stain Protein Labeling Reagent is a fast, easy-to-use, covalent protein labeling reagent, applied to a gel or a membrane after protein transfer that provides sensitive, linear...
The attachment of fluorescent dyes to proteins and other biomolecules is a common strategy used to better understand protein structure and function. These fluorescent proteins can be used in a broad range of applications including immunochemistry, fluorescence in situ hybridization (FISH), cell...
The Invitrogen iBright Imaging Systems capture images and analyze data from your western blots and gels efficiently and easily. With a blend of modern design and performance, iBright Imaging Systems enhance your imaging workflow.
The iBright Imaging Systems offer up to five imaging modes to support your multiple application requirements. Efficiently and easily capture data from protein gels, nucleic acid gels, chemiluminescent western blots, fluorescent western blots, and more.
Explore protein labeling products Crosslinking Technical Handbook, Biotin is a useful label for protein detection, purification and immobilization because of its extraordinarily strong binding to avidin , streptavidin or Thermo Scientific NeutrAvidin Protein .
Protein gel electrophoresis is a simple way to separate proteins prior to downstream detection or analysis. Our portfolio of high-quality protein electrophoresis products unites gels, gel tanks, protein gel handcast system, stains, molecular weight markers and standards, running buffers, and...
View all What is protein crosslinking? What is protein labeling? What functional groups are available for crosslinking/labeling? How can I store my protein after crosslinking/labeling?, View all After crosslinking/labeling, my protein of interest precipitates out of solution. What can I do?
Western blotting is a multi-step process that can take hours or one to two days to complete, depending on the methods used. Below are videos that detail the common steps used to perform a western blot, from separating proteins in protein gel electrophoresis to developing the blot.
Learn about methods and technologies for protein gel electrophoresis and western blot detection and imaging. Browse this foundation library content by topic to find overview articles, application notes, and technical tips.
Thermo Scientific DyLight microscale protein labeling kits contain NHS ester-activated derivatives of our high-performance DyLight dyes designed specifically for labeling small quantities of antibodies or proteins.
The Qubit Protein Assay Kits are designed to make protein quantification easy while providing accurate quantification. Qubit protein assays require only 10–15 minutes of room temperature incubation, eliminating long incubation periods or exposure to elevated temperatures.
Traditional western blotting is useful for detecting the presence or absence of a specific protein in a lysate or complex mixture. Furthermore, it can provide a qualitative assessment of changes in protein expression levels in response to stimuli or interventions.