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This protein belongs to the aldehyde dehydrogenase family of proteins. Additionally we are shipping ALDH3B1 Kits (12) and ALDH3B1 Proteins (6) and many more products for this protein.
Showing 10 out of 66 products:
Human Polyclonal ALDH3B1 Primary Antibody for EIA, IHC (p) - ABIN360240
Yoon, Nakamura, Arakawa: Identification of ALDH4 as a p53-inducible gene and its protective role in cellular stresses. in Journal of human genetics 2004
Show all 2 references for ABIN360240
Human Polyclonal ALDH3B1 Primary Antibody for EIA, IHC (p) - ABIN360239
Geraghty, Vaughn, Nicholson, Lin, Jimenez-Sanchez, Obie, Flynn, Valle, Hu: Mutations in the Delta1-pyrroline 5-carboxylate dehydrogenase gene cause type II hyperprolinemia. in Human molecular genetics 1998
Show all 2 references for ABIN360239
Human Polyclonal ALDH3B1 Primary Antibody for EIA, WB - ABIN453511
Marchitti, Orlicky, Vasiliou: Expression and initial characterization of human ALDH3B1. in Biochemical and biophysical research communications 2007
Human Polyclonal ALDH3B1 Primary Antibody for ELISA, WB - ABIN4279262
Wang, Hu, Fang, Zhang, Yang, Ma, Xu, Shen: Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia. in Biological psychiatry 2009
Human Polyclonal ALDH3B1 Primary Antibody for IHC, ELISA - ABIN1534613
Hsu, Chang, Yoshida: Cloning of a cDNA encoding human ALDH7, a new member of the aldehyde dehydrogenase family. in Gene 1995
the likely physiological function of ALDH3B1 is to oxidize lipid-derived aldehydes generated in the plasma membrane and not to be involved in the sphingolipid metabolism in the endoplasmic reticulum.
the impact of the hyperprolinemia-associated mutation of Ser352 to Leu on the structure and catalytic properties of the P5CDH (show ALDH4A1 Antibodies)
The specificity of ALDH3B1 distribution may prove to be directly related to the functional role of this enzyme in human tissues.
ALDH4 is transcriptionally induced by p53 (show TP53 Antibodies).
Initial characterization of human ALDH3B1 suggests a potential physiological role of this protein in oxidative stress processes.
These findings provided convincing evidence that epistasis between the catechol-O-methyltransferase (show COMT Antibodies) and aldehyde dehydrogenase 3B1 genes plays an important role in the pathogenesis of schizophrenia
This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
aldehyde dehydrogenase 3 family, member B1
, aldehyde dehydrogenase family 3 member B1-like
, aldehyde dehydrogenase 3B2
, aldehyde dehydrogenase 3B1
, aldehyde dehydrogenase 7
, aldehyde dehydrogenase family 3 member B1
, P5C dehydrogenase
, aldehyde dehydrogenase family 4 member A1
, delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
, mitochondrial delta-1-pyrroline 5-carboxylate dehydrogenase