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anti-Human ALDH6A1 Antibodies:
anti-Rat (Rattus) ALDH6A1 Antibodies:
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Human Polyclonal ALDH6A1 Primary Antibody for IHC (p), ELISA - ABIN544088
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
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Human Polyclonal ALDH6A1 Primary Antibody for IHC (p), ELISA - ABIN544087
Chambliss, Gray, Rylance, Pollitt, Gibson: Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency. in Journal of inherited metabolic disease 2000
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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
Human Polyclonal ALDH6A1 Primary Antibody for ELISA, IHC - ABIN4279274
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
Results show that ALDH6A1 expression is significantly reduced in metastatic prostate cancer and represents a strong marker predicting survival, along with HSP27 and prohibitin.
ACAT1, ACACA, ALDH6A1 and MTHFD1 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.
, methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial
, mitochondrial acylating methylmalonate-semialdehyde dehydrogenase
, aldehyde dehydrogenase family 6 member A1
, aldehyde dehydrogenase family 6, subfamily A1
, methylmalonate semialdehyde dehydrogenase
, aldehyde dehydrogenase 6A1
, aldehyde dehydrogenase 6 family, member A1
, methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial-like
, Malonate-semialdehyde dehydrogenase