Examples of 'coomassie brilliant blue' in a sentence

Meaning of "coomassie brilliant blue"

Coomassie Brilliant Blue is a dye commonly used to stain proteins in gel electrophoresis, allowing them to be visualized for analysis

How to use "coomassie brilliant blue" in a sentence

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coomassie brilliant blue
Protein bands were visualized by staining with coomassie brilliant blue.
Gels were either stained with Coomassie brilliant blue or transferred to nitrocellulose membranes.
The proteic concentration is determined quantitatively by using Coomassie brilliant blue.
Coomassie Brilliant Blue dyes will bind to a wide variety of proteins.
Stain the gel with Coomassie brilliant blue.
After electrophoresis the protein moieties are visualized by staining with Coomassie Brilliant Blue.
The gel is dyed with Coomassie Brilliant Blue or silver to visualize the proteins.
Protein bands were stained with Coomassie brilliant blue.
Coomassie Brilliant Blue and how it changes colors.
The gel was then stained with Coomassie brilliant blue.
Staining with Coomassie Brilliant Blue gave a single band.
Proteins were detected by silver staining or Coomassie brilliant blue staining.
Coomassie Brilliant Blue G-250 exists in two different colour forms, red and blue.
The resulting gels were stained with Coomassie brilliant blue.
Shown is the SDS-PAGE and Coomassie brilliant blue staining of the purified protein fractions.

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The PVDF membrane was stained with Coomassie brilliant blue.
Staining was performed with Coomassie brilliant blue ( BioSafecoomassie Stain, Bio-Rad Laboratories ).
The protein bands are visualized by staining the gel with Coomassie Brilliant Blue.
Gels were either stained with Coomassie Brilliant Blue or blotted onto nitrocellulose membranes.
The gels were automatically coloured according to the Phast System with Coomassie brilliant blue.
Proteins were stained with Coomassie Brilliant Blue according to Rosenfeld et al.
Protein bands were visualised by staining with Coomassie Brilliant Blue.
The gel is stained with Coomassie Brilliant Blue to visualize the proteins.
Bands on the gel were visualized by staining with Coomassie Brilliant Blue.
Gels were fixed and stained by Coomassie Brilliant Blue or Merrill silver stain methods.
Antibodies were separated by SDS PAGE and stained with Coomassie brilliant blue.
The analysis by SDS-PAGE and coomassie brilliant blue staining is shown in figure 2A.
After running of the gel, the protein bands were detected using coomassie brilliant blue staining.
It can be stained with Coomassie brilliant blue R250 and by silver stain.
Bands were easily visualized by staining with Coomassie Brilliant Blue dye.
The gel was stained with Coomassie Brilliant Blue R250 and washed with 7 % acetic acid.
Purity was determined on SDS-polyacrylamide gels stained with Coomassie brilliant blue.
One gel was stained with Coomassie Brilliant Blue and destained.
The gel was processed according to general procedures and stained with Coomassie Brilliant Blue ( CBB ).
Visualization of bands was by Coomassie Brilliant Blue staining / destaining.
Purification of a fusión protein ; SDS-polyacrylamide gel stained for total protein with Coomassie Brilliant Blue.
The gel was stained with Coomassie Brilliant Blue and dried.
Gelatinolytic activity was visualized by staining the gels with 0.5 % Coomassie brilliant blue.
Bands were visualized by staining either with Coomassie brilliant blue R-250 or by silver.
Purity was determined on sodium dodecyl sulfate ( SDS ) - polyacrylamide gels stained with Coomassie brilliant blue.
After electrophoresis, the gels were stained with Coomassie Brilliant Blue R-250 by using the PhastSystem.
Proteins were examined by electrophoresis in a 20 % polyacrylamide gel and staining with Coomassie Brilliant Blue.
After electrophoresis, the gels were stained with Coomassie brilliant blue R, dried, and autoradiographed.
After completion of the electrophoresis both gels were stained with Coomassie brilliant blue ( Fig . 5 ).
The most popular protein stain is Coomassie Brilliant Blue.
Following transfer to a nitrocellulose membrane, protein was stained with Coomassie Brilliant Blue R250.
Then the protein was stained with Coomassie Brilliant Blue.
A, Pollen extract was reduced and separated by SDS-PAGE, followed by staining with Coomassie Brilliant Blue.
The gels were stained for protein with Coomassie Brilliant Blue stain.
After electrophoresis, the gels were stained using Coomassie Brilliant Blue.

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