ALDH3A2 抗体
(Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
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60 results
ALDH3A2
适用: 人, 小鼠, 大鼠, 兔, 猴, Pig, 小鸡
WB, IHC, IHC (p)
宿主: 兔
Polyclonal
unconjugated
2 images
ALDH3A2
适用: 人
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 750
ALDH3A2
适用: 人
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 680
Latest Publications for our ALDH3A2 抗体
: "Comparative analysis of proteome and transcriptome variation in mouse. ..." in: PLoS genetics, Vol. 7, Issue 6, pp. e1001393, (2011) (PubMed).
: "Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome." in: Journal of lipid research, Vol. 49, Issue 2, pp. 410-9, (2008) (PubMed).
: "Dual subcellular localization in the endoplasmic reticulum and peroxisomes and a vital role in protecting against oxidative stress of fatty aldehyde dehydrogenase are achieved by alternative splicing." in: The Journal of biological chemistry, Vol. 282, Issue 28, pp. 20763-73, (2007) (PubMed).
: "Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency." in: Molecular genetics and metabolism, Vol. 90, Issue 1, pp. 1-9, (2006) (PubMed).
: "Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2." in: Human mutation, Vol. 24, Issue 2, pp. 186, (2004) (PubMed).
: "Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome." in: Journal of lipid research, Vol. 49, Issue 2, pp. 410-9, (2008) (PubMed).
: "Dual subcellular localization in the endoplasmic reticulum and peroxisomes and a vital role in protecting against oxidative stress of fatty aldehyde dehydrogenase are achieved by alternative splicing." in: The Journal of biological chemistry, Vol. 282, Issue 28, pp. 20763-73, (2007) (PubMed).
: "Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency." in: Molecular genetics and metabolism, Vol. 90, Issue 1, pp. 1-9, (2006) (PubMed).
: "Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2." in: Human mutation, Vol. 24, Issue 2, pp. 186, (2004) (PubMed).
Aliases for ALDH3A2 抗体
aldehyde dehydrogenase 3 family member A2 (ALDH3A2) 抗体aldehyde dehydrogenase family 3, subfamily A2 (Aldh3a2) 抗体
aldehyde dehydrogenase 3 family, member A2 (Aldh3a2) 抗体
Aldehyde dehydrogenase type III (Aldh-III) 抗体
fatty aldehyde dehydrogenase (PTRG_02589) 抗体
aldehyde dehydrogenase 3 family, member A2 (aldh3a2) 抗体
aldehyde dehydrogenase 3 family, member A2a (aldh3a2a) 抗体
aldehyde dehydrogenase 3 family member A2 S homeolog (aldh3a2.S) 抗体
aldehyde dehydrogenase 3 family, member A2 (ALDH3A2) 抗体
aldehyde dehydrogenase 3 family member A2 (aldh3a2) 抗体
aldH (aldH) 抗体
aldehyde dehydrogenase 3 family member A2 (Aldh3a2) 抗体
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