Table 1 Qualitative appraisal of different specimen preparation protocols with effects on the degree of preservation quality (pres.) and contrasting (cont.) of selected subcellular structures visible at the acquired magnification.

From: 3-D EM exploration of the hepatic microarchitecture – lessons learned from large-volume in situ serial sectioning

Cellular structures

SCF

GOT

TAMOI

ROUM

NCMIR

Pres.

Cont.

Pres.

Cont.

Pres.

Cont.

Pres.

Cont.

Pres.

Cont.

Plasma membrane

+

+

+

+

++

++

++

++

+++

+++

Rough endoplasmic reticulum

+

+

+

+

+++

++

+++

+++

Mitochondria

±

±

+

+

++

++

+++

+++

Lipid droplets

++

+

+

++

+++

+++

+++

+++

+++

++

Glycogen

nv

nv

nv

nv

+

+

+++

++

+++

+++

Nuclear membrane

+

±

+

+

++

+

+++

++

+++

+++

Chromatin

++

±

++

±

+++

++

+++

+++

+++

+++

Nucleoli

++

+

+

+

++

+

+++

+

+++

+++

  1. Criteria used in assessing fixation quality based on morphology: (nv) not visible; (−) poor; (±) satisfactory; (+) good; (++) very good; (+++) excellent.
  2. SCF, standard chemical fixation; GOT, glutaraldehyde-osmium tetroxide-tannic acid; TAMOI, tannic acid mediated osmium impregnation; ROUM, reduced osmium and en bloc uranyl acetate method; NCMIR, National Centre for Microscopy and Imaging Research.