Luxol Fast Blue Arn: A New Solvent Azo Dye with Improved Staining Qualities for Myelin and Phospholipids
- 1 January 1962
- journal article
- research article
- Published by Taylor & Francis in Stain Technology
- Vol. 37 (5) , 313-316
- https://doi.org/10.3109/10520296209114492
Abstract
Luxol fast blue ARN (Du Pont, C.I. solvent blue 37) is a diarylguanidine salt of a sulfonated azo dye. This dye was compared with other Luxol blue and Luxol black dyes. Luxol fast blue ARN has improved staining qualities for phospholipids and myelin, and can advantageously be substituted for Luxol fast blue MBS (MBSN). Appropriate staining times for a 0.1% dye solution in 95% ethanol (containing 0.02% acetic add) at 35°-40° C range from 2-3 hr. After staining, the sections should be rinsed in 95% ethanol, rinsed in distilled water, and differentiated for 2 sec in 0.005% Li2CO3, rinsed in 70% ethanol, washed in water, and counterstained as required. Phospholipids and myelin selectively stain deep blue. A fixative containing CaCl2, 1%; cetyltrimethylammonium bromide, 0.5%; and formaldehyde, 10%, in water gave excellent results with brain. However, 10% formalin can be used. The staining of the phospholipids is probably due to the formation of dye-phospholipid complexes.Keywords
This publication has 9 references indexed in Scilit:
- A Quantitative Histochemical Method for estimating PhospholipidsNature, 1962
- Phospholipids and SulpholipidsNature, 1961
- Simultaneous Specific Demonstration of Thyrotroph, Gonadotroph and Acidophil Cells in the Anterior HypophysisStain Technology, 1960
- Luxol Fast Blue as a Selective Stain for Alpha Cells in the Human PituitaryStain Technology, 1959
- Luxol Fast Blue Combined With the Periodic Acid-Schiff Procedure for Cytological Staining of KidneyStain Technology, 1959
- NEW APPLICATIONS OF THE LUXOL FAST BLUE MYELIN STAIN1956
- Two Organic Fixatives for Acid MucopolysaccharidesStain Technology, 1956
- A Method for the Combined Staining of Cells and Fibers in the Nervous SystemJournal of Neuropathology and Experimental Neurology, 1953