DCX 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00001641-T01

Size

Price

Stock

Quantity

Size:100 uL
Price: USD $ 247.00
Stock:
order now, ship in 6 weeks
abnova-minus
abnova-plus

* The price is valid only in USA. Please select country.

Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

DCX transfected lysate

Western Blot
QC Test

Western Blot

Lane 1: DCX transfected lysate ( 40 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-DCX full-length

    Host

    Human

    Theoretical MW (kDa)

    40

    Interspecies Antigen Sequence

    Mouse (98); Rat (98)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-DCX antibody (H00001641-B01) by Western Blots.

    SDS-PAGE Gel

    DCX transfected lysate

    Western Blot

    Lane 1: DCX transfected lysate ( 40 KDa).
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — DCX

    Entrez GeneID

    1641

    GeneBank Accession#

    NM_178151

    Protein Accession#

    NP_835364

    Gene Name

    DCX

    Gene Alias

    DBCN, DC, LISX, SCLH, XLIS

    Gene Description

    doublecortin

    Omim ID

    300067 300121

    Gene Ontology

    Hyperlink

    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

    Other Designations

    OTTHUMP00000062892|doublecortex|doublin|lissencephalin-X

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
4 Products to Compare
Remove All