RDH5 anticorps (Middle Region)

N° du produit ABIN5516226

Détail du produit anti-RDH5 anticorps

Antigène: RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))

Épitope: Middle Region

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RDH5 est non-conjugé

Application: Western Blotting (WB)

Séquence: RGFRVLASCL TPSGAEDLQR VASSRLHTTL LDITDPQSVQ QAAKWVEMHV

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle terminal region of human RDH5

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur RDH5

Antigène: RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))

Autre désignation: RDH5 (RDH5 Produits)

Synonymes: anticorps 9cRDH, anticorps HSD17B9, anticorps RDH1, anticorps SDR9C5, anticorps RDHB, anticorps MGC84134, anticorps RDH5, anticorps rdh1, anticorps hsd17b9, anticorps im:6901729, anticorps si:dkey-102c8.5, anticorps 9-cis, anticorps AI987873, anticorps RDH4, anticorps cRDH, anticorps retinol dehydrogenase 5, anticorps retinol dehydrogenase 1, anticorps retinol dehydrogenase 5 L homeolog, anticorps retinol dehydrogenase 5 (11-cis/9-cis), anticorps RDH5, anticorps rdh1, anticorps rdh5.L, anticorps rdh5, anticorps Rdh5

Sujet: This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.

Alias Symbols: RDH1, 9cRDH, SDR9C5, HSD17B9

Protein Size: 318

ID gène: 5959

NCBI Accession: NM_001199771, NP_001186700

UniProt: Q92781