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// Workers AI · dad joke modeWhat did DiOC6 say to DiOC6? Let's bond.

From Wikipedia, the free encyclopedia
DiOC6[1]
Names
IUPAC name
3-Hexyl-2-[3-(3-hexyl-2(3H)benzoxazolylidene)-1-propenyl]benzoxazolium iodide
Other names
3,3′-Dihexyloxacarbocyanine iodide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.155.178 Edit this at Wikidata
UNII
  • InChI=1S/C29H37N2O2.HI/c1-3-5-7-13-22-30-24-16-9-11-18-26(24)32-28(30)20-15-21-29-31(23-14-8-6-4-2)25-17-10-12-19-27(25)33-29;/h9-12,15-21H,3-8,13-14,22-23H2,1-2H3;1H/q+1;/p-1 X markN
    Key: XVLXYDXJEKLXHN-UHFFFAOYSA-M X markN
  • InChI=1/C29H37N2O2.HI/c1-3-5-7-13-22-30-24-16-9-11-18-26(24)32-28(30)20-15-21-29-31(23-14-8-6-4-2)25-17-10-12-19-27(25)33-29;/h9-12,15-21H,3-8,13-14,22-23H2,1-2H3;1H/q+1;/p-1
    Key: XVLXYDXJEKLXHN-REWHXWOFAI
  • [I-].o1c4ccccc4[n+](c1C=CC=C3Oc2ccccc2N3CCCCCC)CCCCCC
Properties
C29H37IN2O2
Molar mass 572.531 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

DiOC6 (3,3′-dihexyloxacarbocyanine iodide) is a fluorescent dye used for the staining of a cell's endoplasmic reticulum,[2] vesicle membranes and mitochondria.[3] Binding to these structures occurs via the dye's hydrophilic groups. DiOC6 can be used to label living cells, however they are quickly damaged due to the dye's extreme phototoxicity, so cells stained with this dye can only be exposed to light for short periods of time. When exposed to blue light, the dye fluoresces green.

See also

[edit]

References

[edit]
  1. 3,3′-Dihexyloxacarbocyanine iodide at Sigma-Aldrich
  2. Terasaki M. (1989). "Fluorescent labeling of endoplasmic reticulum". Methods Cell Biol. 29: 125–35. doi:10.1016/s0091-679x(08)60191-0. PMID 2643757.
  3. Koning AJ; et al. (1993). "DiOC6 staining reveals organelle structure and dynamics in living yeast cells". Cell Motil Cytoskeleton. 25 (2): 111–28. doi:10.1002/cm.970250202. PMID 7686821.