ENO3 anticorps (AA 400-434) (Cy5)

N° du produit ABIN752042

L’anticorps anti-ENO3 Polyclonal Lapin est utilisé pour la détection de ENO3 dans des échantillons de Humain. Il a été validé pour WB, IF et FACS.

Aperçu rapide pour ENO3 anticorps (AA 400-434) (Cy5) (ABIN752042)

Antigène: ENO3 (Enolase 3 (Beta, Muscle) (ENO3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ENO3 est conjugé à/à la Cy5

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Détail du produit anti-ENO3 anticorps (Cy5)

Épitope: AA 400-434

Fonction: ENO3 Polyclonal Antibody, Cy5 Conjugated

Réactivité croisée: Humain, Souris, Rat

Homologie: Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ENO3

Isotype: IgG

Information d'application

Indications d'application: WB(1:500-2000), IF(1:100-500), Flow-Cyt(1 μg/Test)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur ENO3

Antigène: ENO3 (Enolase 3 (Beta, Muscle) (ENO3))

Autre désignation: Eno3

Sujet:

Synonyms: MSE, GSD13, Beta-enolase, 2-phospho-D-glycerate hydro-lyase, Enolase 3, Muscle-specific enolase, Skeletal muscle enolase, ENO3

Background: ENO3 is also known as beta enolase, one of the three enolase isoenzymes found in mammals. A switch from alpha enolase to beta enolase occurs in muscle tissue during development and ENO3, a homodimer, is found in skeletal muscle cells in the adult and appears to have a function in striated muscle development and regeneration. Mutations can result in decreased stability of the enzyme and be associated with a glycogen storage myopathy. This results in exercise-induced myalgias, generalized muscle weakness and fatigability.

ID gène: 2027

UniProt: P13929