• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Application of spray-freezing to the study of rapid platelet reactions by a quenched-flow approach.

作者信息

Geanacopoulos M, Gear A R

机构信息

Department of Biochemistry, University of Virginia, Charlottesville 22908.

出版信息

Thromb Res. 1988 Dec 15;52(6):599-607. doi: 10.1016/0049-3848(88)90132-6.

DOI:10.1016/0049-3848(88)90132-6
PMID:3232129
Abstract

A spray-freezing approach coupled to quenched-flow techniques has been developed to study rapid (0.3-5.0 s) biochemical and morphological changes during platelet activation. Platelet-rich plasma (PRP) pumped through the quenched-flow system was atomized and quenched within 50 ms in liquid propane at -196 degrees C. Analysis of platelet size and morphology by scanning electron microscopy (SEM) indicated that platelets can be sprayed without morphological damage. The spray-frozen platelets can be subjected to freeze-fracture, freeze-substitution, or freeze-drying procedures for later analysis by electron microscopy. Quenched-flow techniques have permitted investigation of rapid increases in cytosolic calcium protein phosphorylation and morphological changes which occur within 0.5 s after exposure to an activator. The combination of quenched-flow and spray-freezing methodologies should prove useful for studying equally rapid changes in protein distribution in activated platelets by means of electron microscopy coupled with immunocytochemical approaches.

摘要

相似文献

1
Application of spray-freezing to the study of rapid platelet reactions by a quenched-flow approach.
Thromb Res. 1988 Dec 15;52(6):599-607. doi: 10.1016/0049-3848(88)90132-6.
2
Freeze-fracture studies of human blood platelets activated by thrombin using rapid freezing.使用快速冷冻对凝血酶激活的人血小板进行冷冻断裂研究。
Thromb Haemost. 1985 Oct 30;54(3):574-8.
3
Rapid platelet morphological changes visualized by scanning-electron microscopy: kinetics derived from a quenched-flow approach.通过扫描电子显微镜观察到的快速血小板形态变化:源自猝灭流动法的动力学
Br J Haematol. 1984 Mar;56(3):387-98. doi: 10.1111/j.1365-2141.1984.tb03969.x.
4
Freeze-drying of human platelets: influence of saccharide, freezing rate and cell concentration.人血小板的冷冻干燥:糖类、冷冻速率和细胞浓度的影响
Cryo Letters. 2007 May-Jun;28(3):187-96.
5
New observations on the ultrastructure of mammalian conducting airway epithelium: application of liquid propane freezing, deep etching, and rotary shadowing techniques to freeze-fracture.哺乳动物传导气道上皮超微结构的新观察:液态丙烷冷冻、深度蚀刻和旋转阴影技术在冷冻断裂中的应用。
J Ultrastruct Res. 1984 Oct;89(1):23-33. doi: 10.1016/s0022-5320(84)80020-9.
6
Ultra-rapid freezing of thin biological samples.薄生物样本的超快速冷冻。
Scan Electron Microsc. 1980(Pt 2):361-70.
7
A comparative fine structure study of rat cerebral cortex following ultra-rapid freezing and conventional chemical fixation procedures.大鼠大脑皮层经超快速冷冻和传统化学固定程序后的比较精细结构研究。
J Submicrosc Cytol Pathol. 1988 Oct;20(4):691-700.
8
A comparison of the ultrastructure of spray-frozen and freeze-etched or freeze-dried bull and boar spermatozoa with that after chemical fixation.喷雾冷冻与冷冻蚀刻或冷冻干燥的公牛和公猪精子超微结构与化学固定后超微结构的比较。
J Reprod Fertil. 1976 Nov;48(2):285-90. doi: 10.1530/jrf.0.0480285.
9
In situ localization of cartilage extracellular matrix components by immunoelectron microscopy after cryotechnical tissue processing.冷冻技术处理组织后,通过免疫电子显微镜对软骨细胞外基质成分进行原位定位。
J Histochem Cytochem. 1987 Jun;35(6):647-55. doi: 10.1177/35.6.3553318.
10
Improved cryofixation applicable to freeze etching.
Proc Natl Acad Sci U S A. 1971 Sep;68(9):2149-52. doi: 10.1073/pnas.68.9.2149.

引用本文的文献

1
Geldanamycin disrupts platelet-membrane structure, leading to membrane permeabilization and inhibition of platelet aggregation.格尔德霉素破坏血小板膜结构,导致膜通透性增加并抑制血小板聚集。
Biochem J. 2000 Jan 15;345 Pt 2(Pt 2):307-14.