Simplified flat embedding with lowicryl K4M and LR White

1987 ◽  
Vol 5 (1) ◽  
pp. 111-112
Author(s):  
Gregory W. Erdos
Keyword(s):  
Lr White ◽  
1993 ◽  
Vol 26 (4) ◽  
pp. 352-353 ◽  
Author(s):  
Peter A. Vesk ◽  
Teresa P. Dibbayawan ◽  
Maret Vesk
Keyword(s):  
Lr White ◽  

1991 ◽  
Vol 66 (2) ◽  
pp. 89-92 ◽  
Author(s):  
Antonio Migheli ◽  
Angelo Attanasio
Keyword(s):  
Lr White ◽  

1991 ◽  
Vol 23 (8) ◽  
pp. 381-384 ◽  
Author(s):  
Gregor Stransky ◽  
Robert F. Garry ◽  
Steffen Gay
Keyword(s):  
Lr White ◽  

2000 ◽  
Vol 8 (9) ◽  
pp. 34-35
Author(s):  
Tamara Howard
Keyword(s):  
Lr White ◽  
To Come ◽  

We do this two different ways, using polyethylene (PE) molds or aluminum weigh boats, depending on the sample. You can either heat- or UV-cure these molds – just change the type of “lid” on the embedding mold.The PE molds are used when the coverslip can be made to fit in the mold. We use JB-4-type molds, available from your favorite microscopy supplier. The key to using these molds is that they have to be pre-treated…fill the inner cup of the mold with LR White, cover with an aluminum JB-4 chuck (try to have enough resin in the mold to come up around the base of the chuck), and polymerize in a 60° C oven for a day or two, until the resin is hard. The Al chuck can usually be removed by hand, but a flathead screwdriver used as a pry will help pop it off if you have trouble.


1987 ◽  
Vol 35 (11) ◽  
pp. 1261-1266 ◽  
Author(s):  
A W Vorbrodt

An attempt was made to demonstrate the anionic sites on the endothelial cell (EC) surfaces of mouse brain micro-blood vessels (MBVs) after embedding of tissue samples in hydrophilic media: Lowicryl K4M, LR White, and Polyamph-10. As a cationic probe, poly-L-lysine-gold complex (PLG), prepared according to the procedure of Skutelsky and Roth (J Histochem Cytochem 34:693, 1986), was used. In ultra-thin sections of brain samples embedded in Lowicryl K4M and LR White, the anionic sites were demonstrated in the entire cross-section of the vessel wall. After embedding in Polyamph-10, however, the anionic sites could not be detected. Brain capillaries, representing blood-brain barrier type MBVs, showed polar distribution of anionic sites, evidenced by more intense labeling of luminal than of abluminal plasma membrane of the EC. Some differences in labeling of ECs and of basement membrane in arterioles and venules were also noted. The use of cationic gold and the ultra-thin sections of tissue samples embedded in hydrophilic media (Lowicryl K4M and LR White) seems to be a promising new method for detection of anionic constituents located on both luminal and abluminal surfaces of the EC, in the basement membrane, and in other components of the vessel wall.


1988 ◽  
Vol 36 (12) ◽  
pp. 1543-1551 ◽  
Author(s):  
J F White ◽  
J L Hughes ◽  
J S Kumaratilake ◽  
J C Fanning ◽  
M A Gibson ◽  
...  

Elastic tissue is composed of amorphous-appearing elastin and 12-nm diameter microfibrils, one component of which has recently been isolated and characterized as the 31 KD microfibril-associated glycoprotein MAGP. Monospecific antibodies to each of these components have been developed in this laboratory. The parameters that determine optimal localization of colloidal gold probes for post-embedding immunolabeling of elastic tissue components have been systematically studied in a variety of normal and developing tissues in mammals and birds. Protein A-gold probes stabilized with dextran have been shown to provide complexes that remain stable after more than 2 years. Conditions have been defined that permit precise localization within the extracellular matrix of antibodies to MAGP and to elastin, singly and together. Best results were obtained with acrylic resins (Lowicryl K4M or LR White). Fixation in glutaraldehyde or other aldehydic fixatives, with or without osmium, did not affect the immunostaining of elastic tissue with affinity-purified antibodies to tropoelastin, or to anti-[alpha-elastin] or anti-[alkali-insoluble elastin]. Immunostaining with the anti-MAGP antibody was less robust and was possible in tissues which had been fixed only lightly before embedding in Lowicryl K4M or LR White. This staining was enhanced by metaperiodate oxidation of the sections as well as by reduction of the tissues with sodium borohydride en bloc, followed by hyaluronidase digestion of the sections. The effects on immunostaining of a range of enzyme digestions have also been examined. Conditions have thus been defined that make possible detailed study of the relationship between elastic tissue, elastin-associated microfibrils, and other microfibrillar structures in normal and abnormal tissues during development and aging.


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