Involvement in diseaseDefects in ALDH5A1 are the cause of succinate semialdehyde dehydrogenase deficiency (SSADH deficiency) [MIM:271980]. SSADH deficiency is a rare inborn error in the metabolism of 4-aminobutyric acid (GABA) which leads to accumulation of 4-hydroxybutyric acid in physiologic fluids of patients. The disease is characterized by severe ataxia and by mildly retarded psychomotor development.
Sequence similaritiesBelongs to the aldehyde dehydrogenase family.
Ab65469 (1:10) staining human ALDH5A1 in human hepatocarcinoma tissue by immunohistochemistry using formalin fixed, paraffin embedded tissue.
References for Anti-ALDH5A1 antibody (ab65469)
This product has been referenced in:
Marcato P et al. Aldehyde Dehydrogenase Activity of Breast Cancer Stem Cells Is Primarily Due To Isoform ALDH1A3 and Its Expression Is Predictive of Metastasis. Stem Cells29:32-45 (2011).
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