Microwave Setup and Processing Protocol for PELCO BioWave® Pro

Total processing time: ~30 minutes - Resin Polymerisation: 45-75 minutes

Microwave Configuration A

PELCO® EM Pro Vacuum Chamber with PELCO Prep-Eze™ Specimen Holder inside on the PELCO ColdSpot® Pro

Microwave Configuration B

PELCO Prep-Eze™ Specimen Holder on the PELCO ColdSpot® Pro

Microwave Configuration C

PELCO® Microwave Capsule Holder, Polymerisation Stand and PELCO ColdSpot® Pro

FIXATION

Step		Power	Chamber Config.	Time	Reagent Notes
Fixation Glutaraldehyde Vacuum @ 20" Hg	1 step	<200W	A	1min off - 1min on - 3min off	Start with fixative between 4 and 20°C
Fixation Karnovsky's or Formaldehyde* Vacuum @ 20" Hg	Step 1	150W	A	1min on - 1min off - 1min on	Start with fixative between 4 and 20°C
Fixation Karnovsky's or Formaldehyde* Vacuum @ 20" Hg	Step 2	650W	A	10sec on - 20sec off - 10sec on	Start with fixative between 4 and 20°C
Fixation Osmium** Vacuum @ 20" Hg	Step 1	<100W	A	2min on - 2min off - 2min on	Start with fixative between 4 and 20°C
Fixation Osmium** Vacuum @ 20" Hg	Step 2	<100W	A	2min on - 2min off - 2min on	Cool fixative if T>27°C before starting Step 2

*NOTE: Formaldehyde containing fixatives need a two-step fixation process for fresh tissue.

**NOTE: Osmium penetration into tissue is best at low wattage.

DEHYDRATION

Step		Power	Chamber Config.	Time	Reagent Notes
50% ETOH	Step 1	<250W	B	40sec	Start with ETOH or acetone at room temperature
70% ETOH	Step 2	<250W		40sec
90% ETOH	Step 3	<250W		40sec
100% ETOH	Step 4	<250W		40sec
100% ETOH	Step 5	<250W		40sec

NOTE: the same steps can be used for acetone in place of ETOH.

RESIN INFILTRATION

(Vacuum @ 20" Hg)

Step		Power	Chamber Config.	Time	Reagent Notes
1:1 acetone:resin	Step 1	>200W	A	3-5min	Resin viscosity will determine wattage and time
100% resin	Step 2	>200W		3-5min
100% resin	Step 3	>200W		3-5min

Spurr's & LR White 200W - Epon 250W - Araldite 300W Use longer times based on sample and resin.

RESIN POLYMERISATION

(Elevate dish above ColdSpot with vacuum glass ring)

Step		Power	Chamber Config.	Time	Reagent Notes
Epoxy	Step 1	150W	C	30min	The first 30 minutes of heating should not exceed 60°C for best results
Epoxy	Step 2	750W		60min
LR White	Step 1	150W		30min
LR White	Step 2	750W		30min

(1) Use temperature probe to check solution temperature after the microwave step is completed.

The temperature probe will act as a microwave antenna in small fluid volumes creating a sample temperature profile that would not exist otherwise.

The protocol above is based on:

Giberson, R.T., Austin, R.L., Charlesworth, J., Adamson, G., Herrera, G.A. (2003) Microwave and digital imaging technology reduce turnaround times for diagnostic electron microscopy. Ultrastruct. Pathol. 27:187-196.

Microwave-assisted tissue processing for electron microscopy is no different from conventional processing methods. The reagents used on the bench are typically used in the microwave. The number of steps in conventional processing are usually converted into microwave steps.

Microwave-assisted Fixation:

The microwave steps for fixation are programmed differently for glutaraldehyde than for fixation with formaldehyde or formaldehyde containing fixatives such as Karnovsky's (see appendix). Recent work (see below) has demonstrated the need for two different wattage settings when formaldehyde is used alone or as part of a mixed fixative.

Galvez, J.J., Giberson, R.T., Cardiff, R.D. (2006) The role of microwave radiation in reducing formaldehyde fixation times. The J. Histotechnol. 29:113-121.

The specimen holder routinely used for microwave processing is the PELCO Prep-Eze™ Kit (Fig. 1). There is also a microcentrifuge tube holder (Fig. 1) supplied with the EM Kit. The Prep-Eze™ is placed in 58 x 15mm polypropylene petri dishes which are half- filled with reagent (Figs. 2 & 3).

	The microcentrifuge tube holder can be used for sample fixation and processing as well as the Prep-Eze. The arrow indicates the approximate level to fill the tube for processing. NOTE: More than one Prep-Eze can be processed at one time.They can also be processed side-by-side with the microcentrifuge tube holder.
	The Prep-Eze, designed for bench or microwave sample processing for electron microscopy, is available as a 6-well and 12-well kit. The ID Mats shown above can be written on with a Sharpie and the markings removed by wetting a towel with acetone and wiping the surface. Taped to the counter they serve as an easy-to-use method of specimen identification.

The Prep-Eze™ is placed in the vacuum chamber for aldehyde and osmium fixation, en bloc staining and resin infiltration (Figs. 4). The vacuum chamber is then placed on the ColdSpot as shown in Figure 5.

The PELCO BioWave® Pro is programmed with individual protocols for fixation with glutaraldehyde, osmium, ethanol or acetone dehydration, resin infiltration and resin polymerisation (epoxies) as separate protocols. There is also the complete processing protocol incorporating all steps mentioned above. Protocol steps can be edited to suit your processing requirements. Dehydration steps are done with the Prep-Eze™ on the ColdSpot as shown in Figure 6.

Resin polymerisation requires placing the embedding capsules in the PELCO^® Microwave Capsule Holder with Lid and then placing the holder into the Microwave Polymerisation Tray (Figs. 7-10).
The capsule holder is designed for 00 embedding capsules, either conical tip or flat bottomed. The Capsule Preparation Station is designed for filling the embedding capsules with resin and to keep the Microwave Capsule Holder free of any spilled resin during that process.

Appendix:

1. Fixation steps with paraformaldehyde or Karnovsky's fixative - Protocol
Step#	Description	User Prompt (on/off)	Time (hr:min:sec)	Power (Watts)	Temp. (°C)	Load Cooler (off/auto/on)	Vacuum/ Bubble Pump (off/bub/ vac cycle/ vac on)
1	Karnovsky's Fixation On	On	0:1:0	150	50	Auto	Vacuum cycle
2	Karnovsky's Fixation Off	Off	0:3:0	0	50	Auto	Vacuum cycle
3	Karnovsky's Fixation On	Off	0:1:0	150	50	Auto	Vacuum cycle
4	Karnovsky's Fixation Off	Off	0:2:0	0	50	Auto	Vacuum cycle
5	Karnovsky's Fixation On	Off	0:0:10	650	50	Auto	Vacuum cycle
6	Karnovsky's Fixation Off	Off	0:0:20	0	50	Auto	Vacuum cycle
7	Karnovsky's Fixation On	Off	0:0:10	650	50	Auto	Vacuum cycle
8	Buffer Rinse	On	0:0:40	150	50	Auto	Off
9	Buffer Rinse	On	0:0:40	150	50	Auto	Off
10	Osmium On	On	0:2:0	100	50	Auto	Vacuum cycle
11	Osmium Off	Off	0:2:0	0	50	Auto	Vacuum cycle
12	Osmium On	On	0:2:0	100	50	Auto	Vacuum cycle
13	Osmium Off	Off	0:2:0	0	50	Auto	Vacuum cycle
14	Osmium On	On	0:2:0	100	50	Auto	Vacuum cycle
15	Water Rinse	On	0:0:40	150	50	Auto	Off
Notes: Vacuum Cycle = Vacuum and Vent For Continuous Vacuum set vent time to zero

2. En bloc staining steps after osmium fixation - Protocol
Step#	Description	User Prompt (on/off)	Time (hr:min:sec)	Power (Watts)	Temp. (°C)	Load Cooler (off/auto/on)	Vacuum/ Bubble Pump (off/bub/ vac cycle/ vac on)
1	Uranyl Acetate On	On	0:1:0	100	50	Off	Vacuum cycle
2	Uranyl Acetate On	Off	0:1:0	0	50	Off	Vacuum cycle
3	Uranyl Acetate On	Off	0:1:0	100	50	Off	Vacuum cycle

Notes: Vacuum Cycle = Vacuum and Vent. For Continuous Vacuum set vent time to zero

Fig. 1A-C. Figure 1A is a micrograph of a normal sural nerve with a non-myelinated nerve (N) having secretory vesicles (sv), microtubules (mt) and a swan cell nucleus (ScN). The insert (1B) shows a myelinated nerve and the arrows clearly demonstrate its periodicity. Figure 4C is a membranouse Lupus nehpritis (RPS/ISN Class V). There is diffuse, generalized effacement of the foot processes of the visceral epithelial cells. Numerous regularly disposed epimembraneous immune complex deposits are illustrated by the arrows. Both tissues were initially fixed in a variant of 10% NBF (Carson et al. 1972) and then processed in the microwave for ultrastructural evaluation by the methods of Giberson et al. (2003) and Austin (2002). Micrographs from Ronald L. Austin, Research Associate, Dept. of Pathology, LSU Medical Center, Shreveport, LA 71130.

Figure 2A-G. Fig. 2A-B shows cytoplasmic iridovirus from the skin of a sturgeon. The iridovirus is a large enveloped dsDNA virus which infects both insect and vertebrate hosts. Fig. 2C-E demonstrates an intranuclear baculovirus from the hepatopancreas of a crayfish from Northern California. Fig. 2C is a low magnification image of the enveloped dsDNA virus showing the intranuclear arrangement of virus particles Fig. 2D is a higher magnification showing both a cross-sectional and longitudinal view of the virus. Fig. 2E is a high magnification cross-section of a number of virus particles demonstrating the unique intranuclear membrane-bound virions. Fig. 2F-G demonstrates an endothelial cell polyoma virus from a blood vessel in the liver of a parakeet. Polyoma virus have a single molecule of circular dsDNA and the particles are non-enveloped. Polyoma virions are spherical in outline and typically 45nm in diameter. Fig. 2F is a low magnification image showing typical nuclear presentation. Fig. 2G is a high magnification view of the virus. Infected tissues were processed directly from 10% NBF by the microwave methods of Nordhausen and Barr (2001) and Nordhausen et al. (2002). Micrographs from Bob Nordhausen, Univ. of California, Davis, California Animal Health and Food Safety Lab, School of Veterinary Medicine, Davis, CA 95616.

Figure 3. Micrographs from a 2008 microwave workshop held at the Center for Microscopy, San Joaquin Delta College, Stockton, CA. Rat brain (not perfusion fixed) (1), cardiac muscle (2), kidney (3) and liver (4) were processed from osmium through resin polymerization for a net turnaround time of under 4 hours from fresh tissue to the electron microscope. Microwave techniques (Giberson, et al., 2003) make it possible to teach and in real time demonstrate the techniques of electron microscopy.