Ted Pella公司的微波技術(shù)及方法帶來了組織處理領(lǐng)域的一場革新

1. 的ColdSpot™技術(shù)（美國號6329645）
2. 真正的可變功率
3. 數(shù)字化程序控制
4. 內(nèi)置真空及水循環(huán)系統(tǒng)
5. 自動磁電管預(yù)熱
6. 外置SteadyTemp™水溫控制

1. 電鏡組織處理
2. 免疫標(biāo)記
3. 甲醛固定及EDTA脫鈣
4. 石蠟組織處理
5. 共焦顯微鏡及原位雜交

友好的運行界面 所有的參數(shù)都直觀、清晰的顯示在一個屏幕中
生動的運行-時間圖表 可迅速便捷的查看當(dāng)前執(zhí)行程序的實時運行狀況
簡潔的方法選擇 圖標(biāo)化的界面讓用戶瞬間就可以找到所需程序
全新的方法管理功能 每個用戶都可以直接在設(shè)備里創(chuàng)建自己的文件夾，用來存放所需程序，或者將程序直接導(dǎo)入U盤里。因此，BioWave® Pro+非常適合中心實驗室或多用戶實驗室。

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) s 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 s 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 ing the intranuclear arrangement of virus particles Fig. 2D is a higher magnification ing 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 ing 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.

Figure 4A-F. Figures A-C are of normal mouse liver benched fixed in 10% NBF for 24 hours. Figures D-F are of normal mouse liver fixed in 10% NBF for 20 minutes utilizing microwave radiation. All tissues were prepared for fixation identically and cut to 2mm prior to fixation. Figures A and D are corresponding Hematoxylin and Eosin stained sections and figures B and E are corresponding Vimentin IHC stained sections. Figures C and F are corresponding EM sections demonstrating complimentary ultra-structure. Images are from Dr. Jose Galvez, Center for Comparative Medicine and Department of Medical Pathology, University of California, Davis, CA.

Figure 5. Tissues formalin fixed and paraffin processed by the protocols described in Galvez et al. 2006. Mouse mammary tumor virus induced mammary carcinoma (A, B). Note the mitotic figures (arrows) in B. Mouse esophagus with clearly identifiable muscle striations (*) (C). Mouse uterus stained with mouse anti-estrogen (D). (Center for Comparative Medicine and Department of Pathology, Univ. of Calif., Davis)

Figure 6: Confocal projection of Elodea canadensis labeled with Hoechst 33258 nucleic acid probe (blue stain) for 6 minutes in the absence (A) and presence (B) of 150W microwave radiation. Confocal projection of Arabidopsis thaliana root tip labeled with Hoechst 33258 nucleic acid probe after 6 minutes of 150W microwave radiation (C). Confocal projection of in situ hybridization patters of whole chromosome probes (red) hybridized to nuclei of paraffin embedded rabbit skin (D). Confocal projection of mouse kidney paraffin sections labeled with anti-Factor VIII monoclonal antibody for 60 minutes on the bench (E) and after 6 minutes of 150W radiation (F) (Scale for all bars = 50µm) (Table 1). (Mark Sanders, Imaging Center, College of Biological Sciences, Univ. of Minnesota, St. Paul, MN). Reprinted with permission of Galvez et al., Microscopy and Analysis, Nov. 2006.

Figure 7. Retinas were fixed in 4% paraformaldehyde in 0.1M phosphate buffer (pH 7.4) overnight at 4°C. Following fixation the tissue was rinsed 6 x 20 minutes in buffer prior to beginning antibody labeling. The bench staining protocol required 7 days. The labeling results were completed in an afternoon using microwave-enhanced labeling during a workshop held at the Univ. of Minnesota Imaging Center (Mark Sanders, Director - May 17-19, 2006). The retinas were triple-labeled for: Collagen Type IV (basal lamina surrounding blood vessels) with rabbit anti-type IV collagen and the secondary conjugated to FITC (green label) Glutamine Synthetase (enzyme found in retinal Müller glial cells) with mouse anti- glutamine synthetase and the secondary conjugated to Cy3 (red label) Glial Fibrillary acidic protein (GFAP an intermediate filament protein of astroglial cells) with chicken anti-glial fibrillary acidic protein and the secondary conjugated to Cy5 (blue label) Primary antibody labeling was done at 170W for 12 minutes (4 on - 4 off - 4 on) under vacuum (15" Hg). Secondary antibody labeling was done at 170W for 6 minutes (2 on - 2 off - 2 on) under vacuum (15" Hg). Images were collected on a Nikon C1si Confocal Microscope.

Figure 8. Note the symmetrical pattern of demineralization when microwave methods are employed. The separated piece at the top broke off during plastic embedding. From the work of Steven P. Tinling (Tinling et al., 2004), Otolaryngology Research Laboratory, University of California, Davis 95616.

Figure 9. Left Image. Image on the left is an electron micrograph of an inner hair cell (IHC) and supporting cells (S) from a Japanese macaque monkey. The lower left arrow indicates the region n at higher magnification in the image to the right. Bar = 3.0µm. Right Image. In the supporting cells next to the inner hair cell, the rough endoplasmic reticulum and microtubules are well-preserved. Bar = 0.5 µm. Reprinted with permission from Madden and Henson, 1997. From a paper on microwave accelerated decalcification by Madden and Henson, Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC.