ALDH7A1 anticorps

N° du produit ABIN7264665

Détail du produit anti-ALDH7A1 anticorps

Antigène: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH7A1 est non-conjugé

Application: Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human ALDH7A1 (NP_001173.2).

Isotype: IgG

Information d'application

Indications d'application: IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ALDH7A1

Antigène: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Autre désignation: ALDH7A1 (ALDH7A1 Produits)

Synonymes: anticorps atq1, anticorps ALDH7A1, anticorps ATQ1, anticorps EPD, anticorps PDE, anticorps antiquitin, anticorps ATQ, anticorps wu:fi34d12, anticorps wu:fi35e06, anticorps Atq1, anticorps D18Wsu181e, anticorps aldehyde dehydrogenase 7 family member A1, anticorps aldehyde dehydrogenase 7 family member A1 L homeolog, anticorps aldehyde dehydrogenase 7 family, member A1, anticorps aldehyde dehydrogenase family 7, member A1, anticorps ALDH7A1, anticorps aldh7a1, anticorps aldh7a1.L, anticorps Aldh7a1

Sujet: The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.

ID gène: 501

UniProt: P49419

Pathways: Sensory Perception of Sound