By Jacob B. Natvig (auth.), Jacob B. Natvig, Øystein Førre, Gunnar Husby, Anne Husebekk, Bjørn Skogen, Knut Sletten, Per Westermark (eds.)
Both scientifically and socially the Vlth overseas Symposium on Amyloidosis, August five - eight, 1990 in Oslo was once an exceptional luck. there have been 3 and a part extensive days. It begun with the outlet rite, rather highlighted with the Norway-Norway multi media express via David Cochron, and ended with a trip to the Edvard Munch museuro and the Farewell Salmon Dinner at the night of August eight (not to omit the "happy birthday" music for Dorothea Zucker-Franklin on the breakfast desk the subsequent morning). In among used to be the highbrow penetration into the technological know-how of amyloidosis and amyloid proteins, and a deepening of many friendships between old and young "amyloidologists", including many of the cultural and ancient beneficial properties of Oslo and Norway. one of the quite a few Ietters of thank you and gratitude that we have got bought, the senior organizer of the former assembly, Takashi lsobe acknowledged it in brief and eloquently: "You have crushed us, you will have played a drama with pleasure and cheer, you could have hosted so well with beautiful secretariat, you've got prepared striking hospitality in each recognize, you actually did for we all" Now we're left with the lawsuits publication for the 3 coming years until eventually the subsequent symposium in Kingston, Canada, to be able to be equipped by means of Drs. Robert Kisilevsky and Thomas Muckle from the dept of Pathology at Queens collage in 1993. The medical contributions herein disguise the entire periods of the meeting.
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Additional info for Amyloid and Amyloidosis 1990: VIth International Symposium on Amyloidosis August 5–8, 1990, Oslo, Norway
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Materials. Antibodies to apo SAA were raised in sheep as reported be fore (12). 5 g/1 (final concentration) and plasma was obtained by immediate low speed centrifugation and kept at 4°C for a maximum of one day before use. Thawing and refreezing up to three times in several samples with or without the variant SAA did not change the isofocusing pattern of SAA originally obtained with the same sample when fresh. Isoelectric focusing (IEF) and protein blotting. Plasma was subjected to IEF as described by Menzel et al.
5 g/1 (final concentration) and plasma was obtained by immediate low speed centrifugation and kept at 4°C for a maximum of one day before use. Thawing and refreezing up to three times in several samples with or without the variant SAA did not change the isofocusing pattern of SAA originally obtained with the same sample when fresh. Isoelectric focusing (IEF) and protein blotting. Plasma was subjected to IEF as described by Menzel et al. ( 13) with an ampholite pH-range of 3-9. After IEF proteins were electrophoretically blotted onto nitrocellulose sheets and SAA was detected by peroxidase labelad anti sheep antibodies in the presence of 4-chloro-1-naphthol.