| ALDH-2 | aldehyde dehydrogenase |
|---|---|
| ALDH-3 | aldehyde dehydrogenase |
| Gomori's aldehyde fuchsin stain | <technique> A stain used to demonstrate beta cells of the pancreas, storage form of thyrotrophic hormone in beta cells of the anterior pituitary, hypophyseal neurosecretory substance, mast cells, granules, elastic fibres, sulfated mucins, and gastric chief cells. (05 Mar 2000) |
|---|---|
| methyl aldehyde | <chemical> Commonly used fixative and antibacterial agent. As a fixative it is cheap and tends to cause less denaturation of proteins than does glutaraldehyde, particularly if used in a well buffered solution (buffered formalin, formal saline). Old formaldehyde solutions usually contain cross linking contaminants and it is therefore often preferable to used a formaldehyde generating agent such as paraformaldehyde. Formalin fumes, particularly in conjunction with hydrochloric acid vapour, are potently carcinogenic. (20 Jun 2000) |
| cinnamic aldehyde | 3-phenylpropenal;chief constituent of cinnamon oil. Synonym: cinnamic aldehyde. (05 Mar 2000) |
| molybdenum-iron protein aldehyde oxidoreductase | <enzyme> Related to xanthine oxidase; isolated from desulfovibrio gigas Registry number: EC 1.2.7.- Synonym: mop protein (26 Jun 1999) |
| salicylic aldehyde | salicyl aldehyde |
| pyruvic aldehyde | CH3-CO-CHO; Pyruvaldehyde;the aldehyde of pyruvic acid; an intermediate of carbohydrate metabolism in certain organisms. Synonym: pyruvic aldehyde. Methylglyoxal bis(guanylhydrazone), 1,1'-[(methylethanediylidene)dinitrilo]diguanidine;an antineoplastic agent. (05 Mar 2000) |
| sugar aldehyde | A sugar that contains an internal acetal. (05 Mar 2000) |
| ketone-aldehyde mutase | <enzyme> An enzyme that catalyses the interconversion of methylglyoxal and lactate, with glutathione serving as a coenzyme. Chemical name: S-Lactoyl-glutathione methylglyoxal-lyase (isomerizing) Registry number: EC 4.4.1.5 (12 Dec 1998) |
| formic aldehyde | <chemical> Commonly used fixative and antibacterial agent. As a fixative it is cheap and tends to cause less denaturation of proteins than does glutaraldehyde, particularly if used in a well buffered solution (buffered formalin, formal saline). Old formaldehyde solutions usually contain cross linking contaminants and it is therefore often preferable to used a formaldehyde generating agent such as paraformaldehyde. Formalin fumes, particularly in conjunction with hydrochloric acid vapour, are potently carcinogenic. (20 Jun 2000) |