EVC2 anticorps (C-Term)

N° du produit ABIN2856532

Cet anticorps Lapin Polyclonal détecte spécifiquement EVC2 dans WB, IF et ICC. Il présente une réactivité envers Humain.

Aperçu rapide pour EVC2 anticorps (C-Term) (ABIN2856532)

Antigène: EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EVC2 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)

Détail du produit anti-EVC2 anticorps

Épitope: C-Term

Réactivité croisée: Souris

Réactivité croisée (Details): Mouse (85 %)

Attributs du produit: Rabbit Polyclonal antibody to EVC2 (Ellis van Creveld syndrome 2)
EVC2 antibody [C3], C-term

Purification: Purified by antigen-affinity chromatography.

Immunogène: Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human EVC2. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: Suggested dilution Reference ICC/IF 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* Western blot1:500-1:3000*

Commentaires:

Positive Control: A431 , H1299 , HeLa , HepG2

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

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

Stock: -20 °C

Stockage commentaire: Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur EVC2

Antigène: EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))

Autre désignation: EVC2

Sujet: This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.

Cellular Localization: Membrane, Multi-pass membrane protein

Poids moléculaire: 148 kDa

ID gène: 132884

Pathways: Signalisation Hedgehog