Facebook
Toll-free:1-888-852-8623

All categories

  • All categories
  • Flow Cytometry Antibodies
  • ELISA Kits
  • MACS Cell Isolation
  • Antibodies and Reagents
  • Apoptosis and Cell Health Detection
  • Metabolism Assays
  • Immunoassays
  • Cell Identification Kits
  • Proteins and Peptides
  • Cell Culture
Please enter the item number/product keyword!
Keyword cannot be empty !
INSERT SYMBOLS:
  • α
  • β
  • γ
  • δ
  • ε
  • ζ
  • η
  • θ
  • κ
  • μ
  • ω
  • σ
  • τ
  • λ
  • ⅩⅢ
  • ⅩⅢ
  • ⅩⅣ
  • ⅩⅤ
  • ⅩⅦ
  • ⅩⅧ
  • UP ↑
All Size Price Qty
100μL $ 320.00
Add to cart

For research use only.

Verified Samples Verified Samples in IF: HepG2
Dilution ICC/IF 1:20-1:100,  
Isotype IgG2a
Host Mouse
Reactivity Human
Applications ICC/IF
Clonality Monoclonal
Immunogen Recombinant Human Doublecortin/DCX Protein
Abbre DCX
Synonyms DBCN,  DC,  LISX,  SCLH,  XLIS,  DCX,  Dbct,  Doublecortex,  doublecortin,  Doublin,  FLJ51296,  Lis X,  Lissencephalin X,  Lissencephalin-X,  Lissencephaly X linked,  Lissencephaly X linked doublecortin,  Lis-X,  Neuronal migration protein doublecortin,  OTTHUMP00000023859,  OTTHUMP00000023860,  OTTHUMP00000216315,  OTTHUMP00000216316
Swissprot
Concentration 1 mg/mL
Buffer 0.2 μm filtered solution in PBS with 10% Trehalose, 0.02% Tween 80, pH7.0
Purification Method Protein A
Research Areas Neuroscience,  Tags & Cell Markers
Clone No. 2D7
Conjugation Unconjugated
Storage This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.
Shipping Ice bag
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.
Other Clones

{{antibodyDetailsPage.numTotal}} Results

Other Formats

{{formatDetailsPage.numTotal}} Results

Unconjugated

  • IF:{{item.impact}}

    Journal:{{item.journal}} ({{item.year}})

    DOI:{{item.doi}}

    Reactivity:{{item.species}}

    Sample Type:{{item.organization}}

  • Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}

Product Information