DFNA5 anticorps (AA 200-280)

N° du produit ABIN7217644

Cet anticorps Lapin Polyclonal détecte spécifiquement DFNA5 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain et Rat.

Aperçu rapide pour DFNA5 anticorps (AA 200-280) (ABIN7217644)

Antigène: DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DFNA5 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-DFNA5 anticorps

Épitope: AA 200-280

Fonction: DFNA5 Polyclonal Antibody

Specificité: DFNA5 Polyclonal Antibody detects endogenous levels of DFNA5 protein.

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

Immunogène: Synthesized peptide derived from the Internal region of human DFNA5 at AA range: 200-280

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:40000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur DFNA5

Antigène: DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))

Autre désignation: DFNA5

Sujet: Rabbit Anti-DFNA5 Polyclonal Antibody,DFNA5, ICERE1, Non-syndromic hearing impairment protein 5, Inversely correlated with estrogen receptor expression 1, ICERE-1,Hearing impairment is a heterogeneous condition with over 40 loci described. Non-syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.,Non-syndromic hearing impairment protein 5

Poids moléculaire: observerd band 54kDa

ID gène: 1687

UniProt: O60443

Pathways: Sensory Perception of Sound