Doublecortin rabbit pAb

Doublecortin rabbit pAb

AO-06-ES4976-100

Doublecortin rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4976
Product nameDoublecortin rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameDCX; DBCN; LISX; Neuronal migration protein doublecortin; Doublin; Lissencephalin-X; Lis-X
Size100μL
Unit price ($)248
Human gene ID1641
Human Swiss-ProtO43602
SourceRabbit
IsotypeIgG
TargetDoublecortin
Fields
Gene nameDCX
Protein nameNeuronal migration protein doublecortin
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID13193
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtO88809
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtQ9ESI7
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Doublecortin. AA range:346-395
SpecificityDoublecortin Polyclonal Antibody detects endogenous levels of Doublecortin protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)38kD
BackgroundThis 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&quo
Functionalternative products:Isoform LIS-XA possesses an alternative exon in 5' and is then translated from an upstream initiation codon. Isoform LIS-XB, isoform LIS-XC and isoform LIS-XD translation starts at the downstream initiation codon, leading to the absence of the 81 first amino acids. Isoform LIS-XC and isoform LIS-XD differ from isoform LIS-XB by a five amino acids and a one amino acid-insertion respectively,disease:A chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).,disease: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, abno
Subcellular locationCytoplasm . Cell projection, neuron projection . Localizes at neurite tips. .
ExpressionHighly 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.

Additional Images

Image 1
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Western Blot analysis of Jurkat cells using Doublecortin Polyclonal Antibody
Image 2
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Western blot analysis of lysates from Jurkat cells, using Doublecortin Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES4976-100
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