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Volumn 4262, Issue , 2001, Pages 373-382

Use of laser scanning confocal and Two-Photon FRET microscopy to image and quantify the co-localization of fluorophore labeled ligands in MDCK epithelial cells

Author keywords

Alexa488; Apical endosome; Cy3; Fluorescence resonance energy transfer (FRET); Laser scanning confocal microscopy; MDCK cells; Two Photon microscopy

Indexed keywords

CELLS; CROSSTALK; ENERGY TRANSFER; FLUORESCENCE; MULTIPHOTON PROCESSES; PROTEINS; SCANNING;

EID: 0034935793     PISSN: 0277786X     EISSN: None     Source Type: Conference Proceeding    
DOI: 10.1117/12.424578     Document Type: Conference Paper
Times cited : (2)

References (16)
  • 5
    • 0032644365 scopus 로고    scopus 로고
    • Multi-photon excitation fluorescence imaging microscopy in the biomedical sciences
    • (1999) SPIE , vol.3604 , pp. 74-82
    • Periasamy, A.1
  • 6
    • 0033739426 scopus 로고    scopus 로고
    • Two-photon excitation energy transfer miscroscopy
    • (2000) SPIE , vol.3921 , pp. 299-304
    • Periasamy, A.1
  • 7
    • 0028009419 scopus 로고
    • Basolateral to apical transcytosis in polarized cells is indirect and involves BFA and trimeric G protein sensitive passage through the apical endosome
    • (1994) J. Cell Biol. , vol.124 , pp. 83-100
    • Barroso, M.1    Sztul, E.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.