ALDH1A2 anticorps

N° du produit ABIN5647735

Détail du produit anti-ALDH1A2 anticorps

Antigène: ALDH1A2 (Aldehyde Dehydrogenase 1 Family, Member A2 (ALDH1A2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH1A2 est non-conjugé

Application: Western Blotting (WB)

Purification: Antigen affinity purified

Immunogène: Amino acids M1-A110 from the human protein were used as the immunogen for the ALDH1A2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Western blot: 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: Prior to reconstitution, store at 4°C. After reconstitution, the ALDH1A2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur ALDH1A2

Antigène: ALDH1A2 (Aldehyde Dehydrogenase 1 Family, Member A2 (ALDH1A2))

Autre désignation: ALDH1A2 (ALDH1A2 Produits)

Synonymes: anticorps Raldh-2, anticorps RALDH(II), anticorps RALDH2, anticorps RALDH2-T, anticorps fb50h01, anticorps raldh2, anticorps AV116159, anticorps Aldh1a7, anticorps Raldh1, anticorps Raldh2, anticorps aldehyde dehydrogenase 1 family, member A2, anticorps aldehyde dehydrogenase 1 family member A2, anticorps aldehyde dehydrogenase family 1, subfamily A2, anticorps Aldh1a2, anticorps ALDH1A2, anticorps aldh1a2

Sujet: Aldehyde dehydrogenase 1 family, member A2, also known as ALDH1A2 or retinaldehyde dehydrogenase 2 (RALDH2), is an enzyme that in humans is encoded by the ALDH1A2 gene. This protein belongs to the aldehyde dehydrogenase family of proteins. The product of this gene is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde. Retinoic acid, the active derivative of vitamin A (retinol), is a hormonal signaling molecule that functions in developing and adult tissues. The studies of a similar mouse gene suggest that this enzyme and the cytochrome CYP26A1, concurrently establish local embryonic retinoic acid levels which facilitate posterior organ development and prevent spina bifida. Four transcript variants encoding distinct isoforms have been identified for this gene.

UniProt: O94788

Pathways: Retinoic Acid Receptor Signaling Pathway