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Mouse Anti-DCX Recombinant Antibody (CBMAB-BR154LY)


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Summary

Host Animal
Mouse
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG
Application
IHC: 1:300-1:500 dilution, WB: 0.1-0.5 μg/ml

Basic Information

Immunogen
Recombinant full length human Lis-A isoform of DCX purified from E. coli
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
50% glycerol
Preservative
5mM sodium azide
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Neuronal migration protein doublecortin
Introduction
Deoxycytidine kinase (DCK) is required for the phosphorylation of several deoxyribonucleosides and their nucleoside analogs. Deficiency of DCK is associated with resistance to antiviral and anticancer chemotherapeutic agents. Conversely, increased deoxycytidine kinase activity is associated with increased activation of these compounds to cytotoxic nucleoside triphosphate derivatives. DCK is clinically important because of its relationship to drug resistance and sensitivity. [provided by RefSeq, Jul 2008]
Entrez Gene ID
Human1641
Mouse13193
Rat84394
UniProt ID
HumanO43602
MouseO88809
RatQ9ESI7
Alternative Names
Neuronal migration protein doublecortin;Doublin;Lissencephalin-X;Lis-X;DCX;DBCN, LISX;
Function
Microtubule-associated protein required for initial steps of neuronal dispersion and cortex lamination during cerebral cortex development. May act by competing with the putative neuronal protein kinase DCLK1 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 PAFAH1B1/LIS-1 of overlapping, but distinct, signaling pathways that promote neuronal migration.
Biological Process
Axoneme assembly Source: GO_Central
Central nervous system development Source: ProtInc
Intracellular signal transduction Source: InterPro
Nervous system development Source: ProtInc
Neuron migration Source: UniProtKB
Photoreceptor cell development Source: GO_Central
Retina development in camera-type eye Source: GO_Central
Cellular Location
Cytoplasm; Neuron projection. Localizes at neurite tips.
Involvement in disease
Lissencephaly, X-linked 1 (LISX1):
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'.
Subcortical band heterotopia X-linked (SBHX):
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.
PTM
Phosphorylation by MARK1, MARK2 and PKA regulates its ability to bind microtubules (By similarity). Phosphorylation at Ser-265 and Ser-297 seems to occur only in neonatal brain, the levels falling precipitously by postnatal day 21 (By similarity).
Ubiquitinated by MDM2, leading to its degradation by the proteasome. Ubiquitinated by MDM2 and subsequent degradation leads to reduce the dendritic spine density of olfactory bulb granule cells.
More Infomation

Bott, C. J., McMahon, L. P., Keil, J. M., Yap, C. C., Kwan, K. Y., & Winckler, B. (2020). Nestin selectively facilitates the phosphorylation of the Lissencephaly-linked protein doublecortin (DCX) by cdk5/p35 to regulate growth cone morphology and Sema3a sensitivity in developing neurons. Journal of Neuroscience, 40(19), 3720-3740.

Manka, S. W., & Moores, C. A. (2020). Pseudo‐repeats in doublecortin make distinct mechanistic contributions to microtubule regulation. EMBO reports, 21(12), e51534.

Leung, J. M., Nagayasu, E., Hwang, Y. C., Liu, J., Pierce, P. G., Phan, I. Q., ... & Hu, K. (2020). A doublecortin-domain protein of Toxoplasma and its orthologues bind to and modify the structure and organization of tubulin polymers. BMC molecular and cell biology, 21(1), 1-25.

Ayanlaja, A. A., Ji, G., Wang, J., Gao, Y., Cheng, B., Kanwore, K., ... & Gao, D. (2020). Doublecortin undergo nucleocytoplasmic transport via the RanGTPase signaling to promote glioma progression. Cell Communication and Signaling, 18(1), 1-17.

Unger, M. S., Marschallinger, J., Kaindl, J., Klein, B., Johnson, M., Khundakar, A. A., ... & Aigner, L. (2018). Doublecortin expression in CD8+ T-cells and microglia at sites of amyloid-β plaques: A potential role in shaping plaque pathology?. Alzheimer's & Dementia, 14(8), 1022-1037.

Liu, J. Y., Matarin, M., Reeves, C., McEvoy, A. W., Miserocchi, A., Thompson, P., ... & Thom, M. (2018). Doublecortin-expressing cell types in temporal lobe epilepsy. Acta neuropathologica communications, 6(1), 1-13.

Moslehi, M., Ng, D. C., & Bogoyevitch, M. A. (2017). Dynamic microtubule association of Doublecortin X (DCX) is regulated by its C-terminus. Scientific reports, 7(1), 1-11.

Boulanger, J. J., & Messier, C. (2017). Doublecortin in oligodendrocyte precursor cells in the adult mouse brain. Frontiers in Neuroscience, 11, 143.

Ayanlaja, A. A., Xiong, Y., Gao, Y., Ji, G., Tang, C., Abdikani Abdullah, Z., & Gao, D. (2017). Distinct features of doublecortin as a marker of neuronal migration and its implications in cancer cell mobility. Frontiers in molecular neuroscience, 10, 199.

Nagayasu, E., Hwang, Y. C., Liu, J., Murray, J. M., & Hu, K. (2017). Loss of a doublecortin (DCX)-domain protein causes structural defects in a tubulin-based organelle of Toxoplasma gondii and impairs host-cell invasion. Molecular biology of the cell, 28(3), 411-428.

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For research use only. Not intended for any clinical use.

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