Literature DB >> 2643757

Fluorescent labeling of endoplasmic reticulum.

M Terasaki1.   

Abstract

The fluorescent molecule, DiOC6(3), can be used to label the ER in living cultured cells. The labeling procedures are simple and rapid, and in optimum conditions, the staining is bright and clear and bleaches slowly. The main disadvantage of the technique is toxicity. Photodynamic damage is probably the most serious of the toxic effects, because the damage can be relatively rapid and because the extent and nature of the damage during exposure to the light cannot be determined. To lessen the damage, the exposure of cells to light should be minimized. For many applications, it would be best to verify that cell function is normal during the experimental observations.

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Year:  1989        PMID: 2643757     DOI: 10.1016/s0091-679x(08)60191-0

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  19 in total

1.  Labeling of mesenchymal stem cells by bioconjugated quantum dots.

Authors:  Bhranti S Shah; Paul A Clark; Eduardo K Moioli; Michael A Stroscio; Jeremy J Mao
Journal:  Nano Lett       Date:  2007-09-22       Impact factor: 11.189

2.  DS28-6, a temperature-sensitive mutant of Chinese hamster ovary cells, expresses key phenotypic changes associated with brefeldin A treatment.

Authors:  C Zuber; J Roth; T Misteli; A Nakano; K Moremen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

3.  Na+ pump low and high ouabain affinity alpha subunit isoforms are differently distributed in cells.

Authors:  M Juhaszova; M P Blaustein
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-04       Impact factor: 11.205

4.  Maintenance of the filamentous actin cytoskeleton is necessary for the activation of store-operated Ca2+ channels, but not other types of plasma-membrane Ca2+ channels, in rat hepatocytes.

Authors:  Ying-Jie Wang; Roland B Gregory; Greg J Barritt
Journal:  Biochem J       Date:  2002-04-01       Impact factor: 3.857

5.  Trafficking of spontaneously endocytosed MHC proteins.

Authors:  I Chiu; D M Davis; J L Strominger
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

6.  In vivo examination of membrane protein localization and degradation with green fluorescent protein.

Authors:  R Y Hampton; A Koning; R Wright; J Rine
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

Review 7.  In vivo imaging of immune cell trafficking in cancer.

Authors:  Luisa Ottobrini; Cristina Martelli; Daria Lucia Trabattoni; Mario Clerici; Giovanni Lucignani
Journal:  Eur J Nucl Med Mol Imaging       Date:  2010-12-18       Impact factor: 9.236

8.  Local subplasma membrane Ca2+ signals detected by a tethered Ca2+ sensor.

Authors:  Moo Yeol Lee; Hong Song; Junichi Nakai; Masamichi Ohkura; Michael I Kotlikoff; Stephen P Kinsey; Vera A Golovina; Mordecai P Blaustein
Journal:  Proc Natl Acad Sci U S A       Date:  2006-08-21       Impact factor: 11.205

9.  A comparison of the emission efficiency of four common green fluorescence dyes after internalization into cancer cells.

Authors:  Yukihiro Hama; Yasuteru Urano; Yoshinori Koyama; Marcelino Bernardo; Peter L Choyke; Hisataka Kobayashi
Journal:  Bioconjug Chem       Date:  2006 Nov-Dec       Impact factor: 4.774

10.  Cell cycle-dependent regulation of structure of endoplasmic reticulum and inositol 1,4,5-trisphosphate-induced Ca2+ release in mouse oocytes and embryos.

Authors:  Greg FitzHarris; Petros Marangos; John Carroll
Journal:  Mol Biol Cell       Date:  2003-01       Impact factor: 4.138

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