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Anti-Doublecortin (phospho S28) antibody - Neuronal Marker
See all Doublecortin products (10) ...
Rabbit polyclonal to Doublecortin (phospho S28) - Neuronal Marker
IHC-FoFr, WBmore details
Reacts with
Mouse, Rat
Predicted to work with
Human
Synthetic peptide conjugated to KLH derived from within residues 1 - 100 of Mouse Doublecortin, phosphorylated at S28.
(Peptide available as ab31511.)
Mouse Adult Brain Whole Tissue Lysate and Mouse (0-days old) Brain Whole Tissue Lysate. Rat adult brain tissue.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.016% Sodium Azide
Constituents: 0.8% BSA, 80mM Boric Acid, 60mM Sodium chloride, 4mM EDTA, 20mM Sodium borate, pH 7.4
Concentration information loading...
Immunogen affinity purified
Doublecortin (DCX) undergoes a cycle of dephosphorylation and phosphorylation that regulates its binding to microtubules in growing neurites. The N-terminus serine-28 is a major site of phosphorylation for DCX; this was identified by Graham et al (2004). Single mutation of Ser-28 reduced but did not abolish phosphorylation; DCX is subject to complex multi-site phosphorylation
Polyclonal
IgG
Tags & Cell Markers >> Cell Type Markers >> Neuroscience Markers >> Neuronal
Neuroscience >> Cell Type Marker >> Neuron marker >> Growth Cone
Neuroscience >> Cell Type Marker >> Neuron marker >> Soma marker
Neuroscience >> Cell Adhesion Proteins >> Cytoskeletal Proteins >> Microtubules
Our Abpromise guarantee covers the use of ab23544 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-FoFr: 1/1000
WB: Use a concentration of 1 µg/mlDetects a band of approximately 50 kDa (predicted molecular weight: 50 kDa).Can be blocked with Doublecortin peptide - phospho S28 (ab31511).
Is unsuitable for or IHC-P.
Seems to be required for initial steps of neuronal dispersion and cortex lamination during cerebral cortex development. May act by competing with the putative neuronal protein kinase DCAMKL1 in binding to a target protein. May in that way participate in a signaling pathway that is crucial for neuronal interaction before and during migration, possibly as part of a calcium ion-dependent signal transduction pathway. May be part with LIS-1 of an overlapping, but distinct, signaling pathways that promote neuronal migration.
Highly expressed in neuronal cells of fetal brain (in the majority of cells of the cortical plate, intermediate zone and ventricular zone), but not expressed in other fetal tissues. In the adult, highly expressed in the brain frontal lobe, but very low expression in other regions of brain, and not detected in heart, placenta, lung, liver, skeletal muscles, kidney and pancreas.
Defects in DCX are the cause of lissencephaly X-linked type 1 (LISX1) [MIM:300067]; also called X-LIS or LIS. LISX1 is a classic lissencephaly characterized by mental retardation and seizures that are more severe in male patients. Affected boys show an abnormally thick cortex with absent or severely reduced gyri. Clinical manifestations include feeding problems, abnormal muscular tone, seizures and severe to profound psychomotor retardation. Female patients display a less severe phenotype referred to as 'doublecortex'.
Defects in DCX are the cause of subcortical band heterotopia X-linked (SBHX) [MIM:300067]; also known as double cortex or subcortical laminar heterotopia (SCLH). SBHX is a mild brain malformation of the lissencephaly spectrum. It is characterized by bilateral and symmetric plates or bands of gray matter found in the central white matter between the cortex and cerebral ventricles, cerebral convolutions usually appearing normal.
Note=A chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).
Contains 2 doublecortin domains.
Cytoplasm.
Target information above from: UniProt accessionO43602
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Doublecortin (phospho S28) antibody - Neuronal Marker (ab23544)

All lanes : Anti-Doublecortin (phospho S28) antibody - Neuronal Marker (ab23544) at 1 µg/ml
Lane 1 : Mouse Adult Brain Whole Tissue Lysate
Lane 2 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188)
Lane 3 : Mouse Adult Brain Whole Tissue Lysate with Doublecortin peptide - phospho S28 (ab31511) at 1 µg/ml
Lane 4 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188) with Doublecortin peptide - phospho S28 (ab31511) at 1 µg/ml
Lane 5 : Mouse Adult Brain Whole Tissue Lysate with Doublecortin peptide (ab31512) at 1 µg/ml
Lane 6 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188) with Doublecortin peptide (ab31512) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution
Performed under reducing conditions.
Predicted band size : 50 kDa
Observed band size : 50 kDa
Additional bands at : 35 kDa (possible degradation product).
Immunohistochemistry - Free Floating - Doublecortin (phospho S28) antibody - Neuronal Marker (ab23544)

Immunofluorescent staining for Doublecortin (phospho S28) in the rat habenular nucleus using Rabbit polyclonal to Doublecortin (phospho S28). The staining pattern observed with ab23544 appears to be specific, however, the staining is not very strong or contrasted - this might be expected for detection of a modification protein in unstimulated tissue. Protocol details: Rats were intracardially perfused with 4% paraformaldehyde. Whole brain tissue was post-fixed overnight in the same fixative, and cryoprotected in 20% sucrose and frozen in OCT. 30µm coronal sections were cut by cyrostat for use in free floating IHC. Primary antibody ab123544 was incubated overnight at 1/1000 at room temperature. Secondary antibody Alexa fluor 488 1/1000 was incubated for 2 hours at room temperature.
S Pezet, Univ London Kings Coll, UK
ab23544 has not yet been referenced specifically in any publications.
Publishing research using ab23544? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-Doublecortin (phospho S28) antibody - Neuronal Marker (ab23544) at 1 µg/ml
Lane 1 : Mouse Adult Brain Whole Tissue Lysate
Lane 2 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188)
Lane 3 : Mouse Adult Brain Whole Tissue Lysate with Doublecortin peptide - phospho S28 (ab31511) at 1 µg/ml
Lane 4 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188) with Doublecortin peptide - phospho S28 (ab31511) at 1 µg/ml
Lane 5 : Mouse Adult Brain Whole Tissue Lysate with Doublecortin peptide (ab31512) at 1 µg/ml
Lane 6 : Brain (Mouse) Tissue Lysate - normal tissue, 0 days old (ab7188) with Doublecortin peptide (ab31512) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution
Performed under reducing conditions.
Predicted band size : 50 kDa
Observed band size : 50 kDa
Additional bands at : 35 kDa (possible degradation product).

Immunofluorescent staining for Doublecortin (phospho S28) in the rat habenular nucleus using Rabbit polyclonal to Doublecortin (phospho S28). The staining pattern observed with ab23544 appears to be specific, however, the staining is not very strong or contrasted - this might be expected for detection of a modification protein in unstimulated tissue. Protocol details: Rats were intracardially perfused with 4% paraformaldehyde. Whole brain tissue was post-fixed overnight in the same fixative, and cryoprotected in 20% sucrose and frozen in OCT. 30µm coronal sections were cut by cyrostat for use in free floating IHC. Primary antibody ab123544 was incubated overnight at 1/1000 at room temperature. Secondary antibody Alexa fluor 488 1/1000 was incubated for 2 hours at room temperature.
S Pezet, Univ London Kings Coll, UK
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