Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.

Human apolipoprotein (apo) B has been recognized to exist in two different forms designated apoB-100 and apoB-48. The two apoB forms are usually separated by NaDodSO4 gel electrophoresis with a low percentage polyacrylamide gel in a tube gel apparatus. However, the matrix of this low percentage gel...

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Main Authors: C Gabelli, D G Stark, R E Gregg, H B Brewer, Jr
Format: Article
Language:English
Published: Elsevier 1988-06-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520388271
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author C Gabelli
D G Stark
R E Gregg
H B Brewer, Jr
author_facet C Gabelli
D G Stark
R E Gregg
H B Brewer, Jr
author_sort C Gabelli
collection DOAJ
description Human apolipoprotein (apo) B has been recognized to exist in two different forms designated apoB-100 and apoB-48. The two apoB forms are usually separated by NaDodSO4 gel electrophoresis with a low percentage polyacrylamide gel in a tube gel apparatus. However, the matrix of this low percentage gel is relatively weak, and one can separate the two forms of apoB in a slab gel apparatus only if one utilizes a gradient polyacrylamide gel or a higher percentage polyacrylamide gel which results in a poorer separation of the protein bands. We have developed an agarose-acrylamide gel electrophoretic method to separate the two major apoB forms. The gel is a mixture of 0.5% agarose and 2% acrylamide. The agarose-acrylamide method is fast, has the advantage of being able to be used on an analytical or preparative scale in a vertical slab gel apparatus, and the gel is of sufficient strength to be used in immunoblotting and/or radioautography.
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spelling doaj.art-62de019081594b4ba982849b386d18ef2022-12-21T20:26:31ZengElsevierJournal of Lipid Research0022-22751988-06-01274457460Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.C GabelliD G StarkR E GreggH B Brewer, JrHuman apolipoprotein (apo) B has been recognized to exist in two different forms designated apoB-100 and apoB-48. The two apoB forms are usually separated by NaDodSO4 gel electrophoresis with a low percentage polyacrylamide gel in a tube gel apparatus. However, the matrix of this low percentage gel is relatively weak, and one can separate the two forms of apoB in a slab gel apparatus only if one utilizes a gradient polyacrylamide gel or a higher percentage polyacrylamide gel which results in a poorer separation of the protein bands. We have developed an agarose-acrylamide gel electrophoretic method to separate the two major apoB forms. The gel is a mixture of 0.5% agarose and 2% acrylamide. The agarose-acrylamide method is fast, has the advantage of being able to be used on an analytical or preparative scale in a vertical slab gel apparatus, and the gel is of sufficient strength to be used in immunoblotting and/or radioautography.http://www.sciencedirect.com/science/article/pii/S0022227520388271
spellingShingle C Gabelli
D G Stark
R E Gregg
H B Brewer, Jr
Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
Journal of Lipid Research
title Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
title_full Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
title_fullStr Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
title_full_unstemmed Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
title_short Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
title_sort separation of apolipoprotein b species by agarose acrylamide gel electrophoresis
url http://www.sciencedirect.com/science/article/pii/S0022227520388271
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AT regregg separationofapolipoproteinbspeciesbyagaroseacrylamidegelelectrophoresis
AT hbbrewerjr separationofapolipoproteinbspeciesbyagaroseacrylamidegelelectrophoresis