Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) ELISA Kits

Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Zusätzlich bieten wir Ihnen ALDH3A2 Antikörper (128) und ALDH3A2 Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
Anti-Human ALDH3A2 ALDH3A2 224 P51648
Anti-Ratte ALDH3A2 ALDH3A2 65183 P30839
Anti-Maus ALDH3A2 ALDH3A2 11671 P47740
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Weitere ELISA Kits für ALDH3A2 Interaktionspartner

Human Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) Interaktionspartner

  1. In female infertility, ALDH3A2 expression levels were higher in patients greater than 40 years of age and in poor responders compared to oocyte donors.

  2. Sjogren-Larsson syndrome belongs to a new group of inborn-errors-of-metabolism with inherited defects in phospholipids, sphingolipids and fatty-acids biosynthesis. It is caused by ALDH3A2 gene mutations.

  3. A previously unreported novel ALDH3A2 mutation was identified, c.681-14T>G, in a Sjogren-Larsson syndrome patient (homozygote) and his asymptomatic parents (heterozygotes).

  4. The gatekeeper helix domain is important for directing the substrate specificity of FALDH (zeige ADH5 ELISA Kits) towards long-chain fatty aldehydes.

  5. Sjogren-Larsson Syndrome patients with ALDH3A2 mutations exhibit retinal disease in retinal cell layers

  6. variation in the neurologic phenotype of Sjogren-Larsson syndrome is not strictly determined by the ALDH3A2 mutation or a biochemical defect, but by unidentified epigenetic/environmental factors, gene modifiers, or other mechanisms.

  7. Five unrelated patients with typical Sjogren-Larsson syndrome all present mutations in the ALDH3A2 gene.

  8. the Sjogren-Larsson syndrome-causative gene ALDH3A2 is responsible for conversion of the sphingosine 1-phosphate degradation product hexadecenal to hexadecenoic acid

  9. We studied three Turkish Sjogren-Larsson syndrome patients One patient was homozygous for a novel ALDH3A2 mutation in exon 5. The mutation involves the codon 228 (CGC) with the transversion G->A modifying the codon in CAC (zeige CA2 ELISA Kits).

  10. We describe 2 Sjogren-Larsson syndrome patients whose disease is caused by large contiguous gene deletions of the ALDH3A2 locus on 17p11.2.

Mouse (Murine) Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) Interaktionspartner

  1. Disruption of the Sjogren-Larsson Syndrome Gene Aldh3a2 in Mice Increases Keratinocyte Growth and Retards Skin Barrier Recovery.

  2. FALDH (zeige ADH5 ELISA Kits) has roles in insulin (zeige INS ELISA Kits) action and is deregulated in states associated with altered insulin (zeige INS ELISA Kits) signaling

ALDH3A2 Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit ALDH3A2

  • aldehyde dehydrogenase 3 family, member A2a (aldh3a2a) Antikörper
  • aldehyde dehydrogenase 3 family, member A2 (ALDH3A2) Antikörper
  • aldehyde dehydrogenase 3 family, member A2 (aldh3a2) Antikörper
  • Aldehyde dehydrogenase type III (Aldh-III) Antikörper
  • aldH (aldH) Antikörper
  • fatty aldehyde dehydrogenase (PTRG_02589) Antikörper
  • Fatty aldehyde dehydrogenase (al3a2) Antikörper
  • aldehyde dehydrogenase 3 family, member A2 (Aldh3a2) Antikörper
  • aldehyde dehydrogenase family 3, subfamily A2 (Aldh3a2) Antikörper
  • Ahd-3 Antikörper
  • Ahd-3r Antikörper
  • Ahd3 Antikörper
  • Ahd3-r Antikörper
  • AI194803 Antikörper
  • ALDH-III Antikörper
  • ALDH3A2 Antikörper
  • Aldh4 Antikörper
  • Aldh4-r Antikörper
  • ALDH10 Antikörper
  • CG11140 Antikörper
  • CT41571 Antikörper
  • Dhap Antikörper
  • Dmel\\CG11140 Antikörper
  • FALDH Antikörper
  • l(2)03610 Antikörper
  • SLS Antikörper
  • wu:fc06b11 Antikörper
  • zgc:92064 Antikörper

Bezeichner auf Proteinebene für ALDH3A2

aldehyde dehydrogenase 3 family, member A2 , fatty aldehyde dehydrogenase , sls , aldehyde dehydrogenase 3A2 , putative aldehyde dehydrogenase family 3 subfamily A2 variant 2 , fatty aldehyde dehydrogenase-like , Aldh-III-PE , Aldh-III-PI , Aldh-III-PK , Aldh-III-PL , Aldh-III-PM , Aldh-III-PN , Aldh-III-PO , Aldh-III-PP , Aldh-III-PQ , Aldh-III-PR , Aldh-III-PS , Aldh-III-PT , Aldh-III-PU , CG11140-PE , CG11140-PI , CG11140-PK , CG11140-PL , CG11140-PM , CG11140-PN , CG11140-PO , CG11140-PP , CG11140-PQ , CG11140-PR , CG11140-PS , CG11140-PT , CG11140-PU , aldehyde dehydrogenase type III , aldehyde dehydrogenase family 3 member A2 , Fatty aldehyde dehydrogenase , aldehyde dehydrogenase 3 family member A2 , aldehyde dehydrogenase 10 , microsomal aldehyde dehydrogenase , alcohol dehydrogenase family 3, subfamily A2 , aldehyde dehydrogenase 4 , aldehyde dehydrogenase family 3, subfamily A2 , msALDH , aldehyde dehydrogenase 3 , aldehyde dehydrogenase 4, liver microsomal (class 3) regulator

GENE ID SPEZIES
323653 Danio rerio
454505 Pan troglodytes
549291 Xenopus (Silurana) tropicalis
703661 Macaca mulatta
100013749 Monodelphis domestica
100073165 Equus caballus
100190154 Taeniopygia guttata
100484362 Ailuropoda melanoleuca
45398 Drosophila melanogaster
1021754 Bifidobacterium longum NCC2705
6340811 Pyrenophora tritici-repentis Pt-1C-BFP
100171557 Pongo abelii
100195398 Salmo salar
100286782 Salmo salar
443767 Xenopus laevis
417615 Gallus gallus
224 Homo sapiens
479518 Canis lupus familiaris
513967 Bos taurus
65183 Rattus norvegicus
100338784 Oryctolagus cuniculus
11671 Mus musculus
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