ArtNr |
ABC-AT1727a |
Hersteller |
Abcepta
|
Menge |
100 ug |
Kategorie |
|
Typ |
Antibody Primary |
Format |
Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
Applikationen |
WB, IF |
Clon |
1G12 |
Specific against |
other |
Host |
Mouse |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Similar products |
DCX, DBCN, LISX, Doublin, Neuronal migration protein doublecortin, Lis-X, Lissencephalin-X |
Lieferbar |
|
Primary Accession |
O43602 |
Antigen Type |
Recombinant Protein |
Application |
WB, IF |
Bio Background |
This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of 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 cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, mental retardation, subcortical band heterotopia (double cortex syndrome) in females and lissencephaly (smooth brain syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene. |
Bio References |
1.LC-MS/MS identification of doublecortin as abundant beta cell-selective protein discharged by damaged beta cells in vitro.Jiang L, Brackeva B, Stangel G, Verhaeghen K, Costa O, Couillard-Despres S, Rotheneichner P, Aigner L, Van Schravendijk C, Pipeleers D, Ling Z, Gorus F, Martens GA.J Proteomics. 2013 Jan 19. doi:pii: S1874-3919(13)00022-5. 10.1016/j.jprot.2012.12.031. |
Clonality |
Monoclonal |
Gene ID |
1641 |
Gene Name |
DCX |
Subtitle |
Mouse monoclonal antibody raised against a full length recombinant DCX. |
Reactivity |
H |
Legend image 1 |
Immunofluorescence of monoclonal antibody to DCX on HeLa cell . [antibody concentration 10 ug/ml] |
Type image 1 |
IF |
Legend image 2 |
Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (65.34 KDa) . |
Type image 2 |
WB |
Dilution image 2 |
1:500~1000 |
Legend image 3 |
Western Blot analysis of DCX expression in transfected 293T cell line by DCX monoclonal antibody (M01), clone 1G12.
Lane 1: DCX transfected lysate(41.4 KDa). Lane 2: Non-transfected lysate. |
Type image 3 |
WB |
Dilution image 3 |
1:500~1000 |
Other Accession |
BC027925 |
Isotype |
IgG1 kappa |
Antigen Source |
Human: ~~ Positive |
Target/Specificity |
DCX (AAH27925, 1 a.a. ~ 360 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
NCBI Accession |
NP_000546.2; NP_835364.1; NP_835365.1; NP_835366.1 |
|
Clone: 1G12 |
Org Accession |
AAH27925 |
Gene Description |
doublecortin |
Gene Summary |
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. [provided by RefSeq |
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