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*CIL – Cell Image Library accession number. Please use this to reference an image.

CIL:37156*  Cite 
Description

Transmission electron micrograph of a cell fractionation of golgi bottom fraction. Image made available by James D. Jamieson and the Department of Cell Biology, Yale University School of Medicine.

Technical Details

The authors took advantage of the fact that rats gavage-fed a large bolus of ethanol were observed to have their Golgi cisternae loaded with LDL particles. Since LDL partlcles are lighter than most other intracellular organelles, following homognenization of ethanol-fed rats, the Golgi fractions "floated" to the top of denser sucrose gradients during centrifugation. This allowed investigators to analyze the membrane properties of "pure" Golgi fractions and set the stage for development of fusion assays that led to an understanding of factors regulating the specificity of membrane fusion - the SNARE hypothesis. An additional technical reference is Ehrenreich et al 1973 JCB 59:45-72. Original 3.25 in. x 4 in. lantern slides were scanned at 600dpi. Original Magnification: x13,750.

Biological Sources
NCBI Organism Classification
Cavia porcellus
Attribution
Names
John Bergeron
George E. Palade
Philip Siekevitz
Link
George E. Palade EM Slide Collection
Citation
Digital Object Identifier (DOI)
doi:10.7295/W9CIL37156
Archival Resource Key (ARK)
ark:/b7295/w9cil37156
Grouping This image is part of a group.
Sample Preparation
Methods
cell fractionation
Relation To Intact Cell
sectioned tissue
Dimensions
Spatial Axis Image Size Pixel Size
X 6000px ——
Y 5265px ——