<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Cell Fractionation smooth microsome fraction guinea pig pancreas</dc:title><dc:creator>Jamieson, James D</dc:creator><dc:date>5/1/1961</dc:date><dc:description>3.25 in. x 4 in. Lantern Slides</dc:description><dc:description>Cell fractionation confirmed that newly synthesized acinar cell secretory proteins moved from the RER to the periphery of the Golgi in the lumen of a smooth-surfaced membrane bounded compartment. This paper also describes the pancreatic slice system and the pulse-chase protocol used to label newly synthesized secretory proteins with radioactive leucine. The micrograph shows smooth microsomes obtained from the top band in the photograph of sucrose density gradient.</dc:description><dc:description>Original Magnification: x10,000</dc:description><dc:format>still image</dc:format></oai_dc:dc>