PEVR2 (AA 235-284) anticorps

N° du produit ABIN1535982

Cet anticorps Lapin Polyclonal détecte spécifiquement PEVR2 dans IF, WB et ELISA. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PEVR2 (AA 235-284) anticorps (ABIN1535982)

Antigène: PEVR2

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Inconjugué

Application: Immunofluorescence (IF), Western Blotting (WB), ELISA

Détail du produit

Épitope: AA 235-284

Fonction: GPR172B Antibody

Specificité: GPR172B Polyclonal Antibody detects endogenous levels of GPR172B protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human PEVR2. AA range:235-284

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Date de péremption: 12 months

Détail du antigène

Antigène: PEVR2

Sujet:

Synonyms: SLC52A1, GPR172B, PAR2, RFT1, Solute carrier family 52, riboflavin transporter, member 1, Porcine endogenous retrovirus A receptor 2, PERV-A receptor 2, Protein GPR172B, Riboflavin transporter 1, hRFT1

Background: Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents.This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013],

Gene Name: SLC52A1

Protein Name: Solute carrier family 52 riboflavin transporter member 1

Poids moléculaire: 46 kDa

ID gène: 55065

OMIM: 607883

UniProt: Q9NWF4