Doublecortin anticorps (AA 362-411)

N° du produit ABIN1844030

L’anticorps anti-Doublecortin Monoclonal Souris est utilisé pour la détection de Doublecortin dans des échantillons de Humain. Il a été validé pour WB, ELISA, IHC, FACS et IF/ICC.

Aperçu rapide pour Doublecortin anticorps (AA 362-411) (ABIN1844030)

Antigène: Doublecortin (DCX)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Doublecortin est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (fixed cells) (IF/ICC)

Détail du produit anti-Doublecortin anticorps

Épitope: AA 362-411

Purification: Purified antibody

Immunogène: Purified recombinant fragment of human DCX (AA: 362-411) expressed in E. Coli.

Isotype: IgG1

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.0 mg/mL

Buffer: PBS with 0.05 % sodium azide and 0.5 % protein stabilizer.

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: Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.

Détails sur Doublecortin

Antigène: Doublecortin (DCX)

Autre désignation: DCX

Sujet: In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The protein encoded by this gene is a cytoplasmic protein which appears to direct neuronal migration by regulating the organization and stability of microtubules. The encoded protein contains two doublecortin domains, which bind microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene are a cause of X-linked lissencephaly. Multiple transcript variants encoding at least three different isoforms have been found for this gene.

Poids moléculaire: 49.3 kDa

ID gène: 1641

UniProt: O43602