Delafield'S Hematoxylin and Safranin for Staining Plant Materials

Abstract

An improved schedule is suggested for staining plant materials in Delafield's hematoxylin and safranin. Tissues are stained first in Delafield's hematoxylin. A short bath in acidulated water (1 or 2 drops concentrated HCl to 100 cc.) removes objectionable precipitates, and at the same time serves as a destaining agent. The acid bath must be followed quickly by a thoro wash in tap water, or dilute lithium carbonate solution, to restore the original dark blue color (made reddish in the acid bath) of the hematoxylin and to “set” the stain. Once the hematoxylin solution is satisfactory, none of the reagents ordinarily used will remove it—unless they contain acid. Tissues are counterstained in rapid safranin (5 drops analin in 100 cc. of 1% safranin 0 in 50% ethyl alcohol); this materially lessens the time necessary for staining. The safranin is de-stained in 50% ethyl alcohol (which does not affect the hematoxylin) until sharp differentiation is secured. If destaining is too slow, or differentiation poor, a quick rinse in acidulated 50% alcohol usually sharpens contrast of the stains. This must be followed quickly by a wash in 50% alcohol containing lithium carbonate to neutralize the acid. Dehydrate, and mount as usual. This schedule allows each stain to be individually, and independently, controlled at the will of the operator.