RDH5 anticorps (AA 24-318)

N° du produit ABIN6146839

Cet anticorps Lapin Polyclonal détecte spécifiquement RDH5 dans WB, IHC et IF. Il présente une réactivité envers Humain.

Aperçu rapide pour RDH5 anticorps (AA 24-318) (ABIN6146839)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RDH5 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Détail du produit anti-RDH5 anticorps

Épitope: AA 24-318

Séquence: LPASNAFVFI TGCDSGFGRL LALQLDQRGF RVLASCLTPS GAEDLQRVAS SRLHTTLLDI TDPQSVQQAA KWVEMHVKEA GLFGLVNNAG VAGIIGPTPW LTRDDFQRVL NVNTMGPIGV TLALLPLLQQ ARGRVINITS VLGRLAANGG GYCVSKFGLE AFSDSLRRDV AHFGIRVSIV EPGFFRTPVT NLESLEKTLQ ACWARLPPAT QAHYGGAFLT KYLKMQQRIM NLICDPDLTK VSRCLEHALT ARHPRTRYSP GWDAKLLWLP ASYLPASLVD AVLTWVLPKP AQAVY

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 24-318 of human RDH5 (NP_002896.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

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 RDH5

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

Autre désignation: 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.,RDH5,9cRDH,HSD17B9,RDH1,SDR9C5,Neuroscience,RDH5

Poids moléculaire: 34 kDa

ID gène: 5959

UniProt: Q92781