Doublecortin antibody (AA 107-137)

Catalog No. ABIN3030770

The Rabbit Polyclonal anti-Doublecortin antibody has been validated for WB, ELISA and IHC. It is suitable to detect Doublecortin in samples from Human.

Quick Overview for Doublecortin antibody (AA 107-137) (ABIN3030770)

Target: Doublecortin (DCX)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Doublecortin antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Product Details anti-Doublecortin Antibody

Binding Specificity: AA 107-137

Cross-Reactivity (Details): Expected species reactivity: Mouse, Rat

Purification: Antigen affinity purified

Immunogen: A portion of amino acids 107-137 from the human protein was used as the immunogen for this DCX antibody.

Isotype: Ig Fraction

Application Details

Application Notes: Titration of the DCX antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

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 the DCX antibody and store frozen at -20°C or colder. 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. DCX is a cytoplasmic protein which appears to direct neuronal migration by regulating the organization and stability of microtubules. It contains two doublecortin domains, which bind microtubules. In addition, this 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 the gene encoding DCX are a cause of X-linked lissencephaly.

UniProt: O43602