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This protein belongs to the aldehyde dehydrogenases family of proteins. Additionally we are shipping ALDH6A1 Kits (5) and ALDH6A1 Proteins (4) and many more products for this protein.
Showing 10 out of 157 products:
Human Monoclonal ALDH6A1 Primary Antibody for WB - ABIN659006
Rose, Behm, Drgon, Johnson, Uhl: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. in Molecular medicine (Cambridge, Mass.) 2010
Show all 5 references for ABIN659006
Human Polyclonal ALDH6A1 Primary Antibody for EIA, IHC (p) - ABIN356978
Chambliss, Gray, Rylance, Pollitt, Gibson: Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency. in Journal of inherited metabolic disease 2000
Show all 2 references for ABIN356978
Human Polyclonal ALDH6A1 Primary Antibody for WB - ABIN517977
Jeon, Jeong, Baek, Koo, Park, Yang, Yu, Kim, Pak: Network clustering revealed the systemic alterations of mitochondrial protein expression. in PLoS computational biology 2011
Chicken Polyclonal ALDH6A1 Primary Antibody for WB - ABIN2782682
Kuiper, Williams, Distl, Drögemüller: Assignment of the PAX6 gene to bovine chromosome 15q25-->q27 by fluorescence in situ hybridization and confirmation by radiation hybrid mapping. in Cytogenetic and genome research 2005
Cow (Bovine) Polyclonal ALDH6A1 Primary Antibody for EIA, WB - ABIN569631
Alnouti, Klaassen: Tissue distribution, ontogeny, and regulation of aldehyde dehydrogenase (Aldh) enzymes mRNA by prototypical microsomal enzyme inducers in mice. in Toxicological sciences : an official journal of the Society of Toxicology 2007
Cow (Bovine) Polyclonal ALDH6A1 Primary Antibody for EIA, IHC (p) - ABIN569630
Hanna, Kruskal, Ezekowitz, Bloom, Collier: Role of macrophage oxidative burst in the action of anthrax lethal toxin. in Molecular medicine (Cambridge, Mass.) 1996
ACAT1 (show ACAT1 Antibodies), ACACA (show ACACA Antibodies), ALDH6A1 and MTHFD1 (show MTHFD1 Antibodies) represent novel biomarkers in adipose tissue associated with type 2 diabetes in obese individuals.
Mutation analysis in the ALDH6A1 gene can reveal a cause of 3-hydroxyisobutyric aciduria, which may present with only slightly increased urinary levels of 3-hydroxyisobutyric acid, if a patient is metabolically stable [case reports]
This protein belongs to the aldehyde dehydrogenases family of proteins. This enzyme plays a role in the valine and pyrimidine catabolic pathways. The product of this gene, a mitochondrial methylmalonate semialdehyde dehydrogenase, catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids.
aldehyde dehydrogenase 6 family, member A1
, mitochondrial acylating methylmalonate-semialdehyde dehydrogenase
, aldehyde dehydrogenase 6A1
, methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial
, methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial-like
, malonate-semialdehyde dehydrogenase
, Malonate-semialdehyde dehydrogenase
, aldehyde dehydrogenase family 6 member A1
, aldehyde dehydrogenase family 6, subfamily A1
, methylmalonate semialdehyde dehydrogenase