Goat Anti-Doublecortin / DCX (aa232-242) Antibody

This goat IgG polyclonal antibody was generated against peptide sequence CKTSANMKAPQS from the internal region of neuronal migration protein doublecortin (DCX) and recognizes human, mouse, and rat DCX.

Highlights:

  • Reacts with human, mouse, and rat DCX
  • Suitable for Peptide ELISA, Western Blot, Immunohistochemistry, and Immunofluorescence applications
  • Mutations in the DCX gene result in lissencephaly or subcortical band heterotopia

Neuronal migration protein doublecortin (DCX) is a microtubule-associated protein that is involved in neuronal migration in embryonic and postnatal brain development. DCX regulates the stability and organization of microtubules by influencing microtuble rigidity, curvature, and the 13-protofilament geometry. Mutations in the DCX gene can lead to epilepsy, cognitive disability, subcortical band heterotopia, and lissencephaly.

Catalog Number Product DataSheet Size AVAILABILITY Price Qty
EB10781
Goat Anti-Doublecortin / DCX (aa232-242) Antibody
100ug specific antibody in 200ul In stock
Regular Price:$415.00
On Sale:
Specifications

Product Type: Antibody
Name: Goat Anti-Doublecortin / DCX (aa232-242) Antibody
Alternative Name(s): Doublin, Lissencephalin-X (Lis-X)
Accession ID: NP_000546.2; NP_835365.1; NP_835364.1; NP_001182482.1
Antigen: Doublecortin / DCX (aa232-242)
Isotype: IgG
Clonality: Polyclonal
Reactivity: Human, Mouse, Rat
Specificity: Doublecortin / DCX (aa232-242)
Immunogen: CKTSANMKAPQS
Species Immunized: Goat
Epitope: Internal Region
Purification Method: Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide
Buffer: Supplied at 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Tested Applications: Pep-ELISA, WB, IHC, IF
Storage: Aliquot and store at -20C. Minimize freezing and thawing.
Shipped: Cold Packs

Documentation
Data

Western Blot, Immunofluorescence, and Immunohistochemistry

WB Data

I. (0.01µg/ml) staining of Mouse fetal Brain lysate (35µg protein in RIPA buffer). Detected by chemiluminescence. II. Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (5ug/ml) followed by Alexa Fluor 488 secondary antibody (1ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (1ug/ml). III. Immunofluorescence analysis of paraformaldehyde fixed KNRK cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml). IV. (2µg/ml) staining of paraffin embedded Human Cerebellum. Microwaved antigen retrieval with citrate buffer pH 6, HRP-staining. V. Negative control showing staining of paraffin embedded Human Cerebellum with no primary antibody.

References
  1. Heysieattalab, S., Sadeghi, Dynamic structural neuroplasticity during and after epileptogenesis in a pilocarpine rat model of epilepsy, Acta Epileptologica 3, 3 (2021). https://doi.org/10.1186/s42494-020-00037-7 ,0

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