anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) Antibodies

Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Additionally we are shipping ALDH3A2 Proteins (9) and and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
ALDH3A2 224 P51648
ALDH3A2 11671 P47740
ALDH3A2 65183 P30839
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Top anti-ALDH3A2 Antibodies at antibodies-online.com

Showing 10 out of 140 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Cow Rabbit Un-conjugated WB WB Suggested Anti-ALDH3A2 Antibody Titration: 0.2-1 ug/ml ELISA Titer: 1:1562500 Positive Control: NCI-H226 cell lysate Host: Rabbit Target Name: ALDH3A2 Sample Type: Human Fetal Lung Antibody Dilution: 1.0ug/ml 100 μL Log in to see 2 to 3 Days
$319.00
Details
Cow Rabbit Un-conjugated IHC, WB WB Suggested Anti-ALDH3A2 Antibody Titration: 0.2-1 ug/ml Positive Control: Jurkat cell lysate Human kidney 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated IHC (p), WB ALDH3A2 was detected in paraffin-embedded sections of human liver cancer tissues using rabbit anti- ALDH3A2 Antigen Affinity purified polyclonal antibody (Catalog # ) at 1 µg/mL. The immunohistochemical section was developed using SABC method (Catalog # SA1022). Western blot analysis of ALDH3A2 expression in rat liver extract ( Lane 1) and 22RV1 whole cell lysates ( Lane 2). ALDH3A2 at 55KD was detected using rabbit anti- ALDH3A2 Antigen Affinity purified polyclonal antibody (Catalog # ) at 0.5 ??g/mL. The blot was developed using chemiluminescence (ECL) method (Catalog # EK1002). 100 μg Log in to see 4 to 6 Days
$280.00
Details
Human Mouse Un-conjugated IHC (p), WB Western blot analysis of ALDH3A2 Antibody in HepG2 cell line lysates (35ug/lane).ALDH3A2 (arrow) was detected using the purified Mab.(1:2000) ALDH3A2 Monoclonal Antibody (Ascites) immunohistochemistry analysis in formalin fixed and paraffin embedded human skin carcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the ALDH3A2 Monoclonal Antibody (Ascites) for immunohistochemistry. Clinical relevance has not been evaluated. 0.1 mL Log in to see 10 to 11 Days
$385.00
Details
Human Goat Un-conjugated IHC, ELISA   100 μg Log in to see 6 to 7 Days
$429.84
Details
Human Goat Un-conjugated ELISA, IHC, WB ABIN571186 (0.03µg/ml) staining of Rat Liver lysate (35µg protein in RIPA buffer). Detected by chemiluminescence. 100 μg Log in to see 6 to 7 Days
$429.84
Details
Mouse Goat Un-conjugated ELISA, WB 0.1 mg Log in to see 2 to 3 Days
$515.63
Details
Human Rabbit Un-conjugated IHC (p), WB Western blot analysis of ALDH3A2 Antibody (ABIN650641) in Hela, HepG2, WiDr cell line lysates (35 µg/lane). ALDH3A2 (arrow) was detected using the purified polyclonal antibody. Formalin-fixed and paraffin-embedded human hepatocarcinoma reacted with ALDH3A2 Antibody, which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. 400 μL Log in to see 10 to 11 Days
$385.00
Details
Mouse Goat Un-conjugated EIA, WB   0.1 mg Log in to see 4 to 8 Days
$462.00
Details
Chicken Rabbit Un-conjugated IHC, IHC (p), WB 50 μg Log in to see 11 to 14 Days
$551.83
Details

Top referenced anti-ALDH3A2 Antibodies

  1. Cow (Bovine) Polyclonal ALDH3A2 Primary Antibody for IHC, WB - ABIN2781793 : Carney, Wei, Rizzo: Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2. in Human mutation 2004 (PubMed)

  2. Mouse (Murine) Polyclonal ALDH3A2 Primary Antibody for ELISA, WB - ABIN4310105 : Rizzo, Craft, Somer, Carney, Trafrova, Simon: Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome. in Journal of lipid research 2008 (PubMed)

  3. Human Polyclonal ALDH3A2 Primary Antibody for IHC, IHC (p) - ABIN4310107 : Ghazalpour, Bennett, Petyuk, Orozco, Hagopian, Mungrue, Farber, Sinsheimer, Kang, Furlotte, Park, Wen, Brewer, Weitz, Camp, Pan, Yordanova, Neuhaus, Tilford, Siemers, Gargalovic, Eskin, Kirchgessner et al.: Comparative analysis of proteome and transcriptome variation in mouse. ... in PLoS genetics 2011 (PubMed)

More Antibodies against ALDH3A2 Interaction Partners

Human Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) interaction partners

  1. Homozygous ALDH3A2 mutations exhibited an unusual neuro-regressive clinical course associated with seizures in Sjogren-Larsson syndrome patients, which may reflect the presence of unidentified genetic or environmental modifiers in this consanguineous population.

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

  3. 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.

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

  5. The gatekeeper helix domain is important for directing the substrate specificity of FALDH towards long-chain fatty aldehydes.

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

  7. 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.

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

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

  10. 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.

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

  12. SLS is caused by mutation in the ALDH3A2 gene, which encodes for FALDH, an enzyme that catalyzes the oxidation of medium- and long-chain aliphtic aldehydes.

  13. The present results suggest that ALDH3A2 is a gene responsible for Sjogren-Larsson syndrome in Asian populations.

  14. Fibroblasts of patients affected by Sjogren Larsson syndrome were found to be deficient in microsomal fatty aldehyde dehydrogenase.

  15. seven novel ALDH3A2 mutations and their associated haplotypes envolved in Sjogren-Larsson Syndrome were identified in 13 patients and one fetus.

  16. REVIEW: mutation update of Sjogren-Larsson syndrome

  17. We report novel compound heterozygous mutations in ALDH3A2 in a Japanese family with Sjogren-Larsson syndrome.

  18. Minireview summarizes recent advances in the molecular genetics of fatty aldehyde dehydrogenase (FALDH) deficiency and the biochemical pathogenesis of Sjogren-Larsson syndrome.

  19. FALDH variants are produced by alternative splicing and share an important role in protecting against oxidative stress in an organelle-specific manner.

  20. These results add to understanding of the genetic basis of Sjogren-Larsson syndrome.

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

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

  2. FALDH has roles in insulin action and is deregulated in states associated with altered insulin signaling

ALDH3A2 Antigen Profile

Protein Summary

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.

Gene names and symbols associated with ALDH3A2

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

Protein level used designations for ALDH3A2

aldehyde dehydrogenase 10 , aldehyde dehydrogenase family 3 member A2 , fatty aldehyde dehydrogenase , microsomal aldehyde dehydrogenase , alcohol dehydrogenase family 3, subfamily A2 , aldehyde dehydrogenase 3 , aldehyde dehydrogenase 4, liver microsomal (class 3) regulator , aldehyde dehydrogenase 3A2 , aldehyde dehydrogenase 4 , aldehyde dehydrogenase family 3, subfamily A2 , msALDH , 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 3 family member A2 , aldehyde dehydrogenase 3 family, member A2 , sls , putative aldehyde dehydrogenase family 3 subfamily A2 variant 2 , fatty aldehyde dehydrogenase-like

GENE ID SPECIES
224 Homo sapiens
11671 Mus musculus
65183 Rattus norvegicus
45398 Drosophila melanogaster
6340811 Pyrenophora tritici-repentis Pt-1C-BFP
100171557 Pongo abelii
100286782 Salmo salar
323653 Danio rerio
417615 Gallus gallus
443767 Xenopus laevis
454505 Pan troglodytes
479518 Canis lupus familiaris
513967 Bos taurus
549291 Xenopus (Silurana) tropicalis
703661 Macaca mulatta
100013749 Monodelphis domestica
100073165 Equus caballus
100190154 Taeniopygia guttata
100338784 Oryctolagus cuniculus
100484362 Ailuropoda melanoleuca
1021754 Bifidobacterium longum NCC2705
100728950 Cavia porcellus
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