Doublecortin antibody (AA 362-411)

Catalog No. ABIN1844030

The Mouse Monoclonal anti-Doublecortin antibody is suitable to detect Doublecortin in samples from Human. It has been validated for WB, ELISA, IHC, FACS and IF/ICC.

Quick Overview for Doublecortin antibody (AA 362-411) (ABIN1844030)

Target: Doublecortin (DCX)

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This Doublecortin antibody is un-conjugated

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

Product Details anti-Doublecortin Antibody

Binding Specificity: AA 362-411

Purification: Purified antibody

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

Isotype: IgG1

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.0 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

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

Target Details for Doublecortin

Target: Doublecortin (DCX)

Alternative Name: DCX

Background: 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.

Molecular Weight: 49.3 kDa

Gene ID: 1641

UniProt: O43602