CNTNAP2 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00026047-T01

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Size:100 uL
Price: USD $ 247.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
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Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

CNTNAP2 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: CNTNAP2 transfected lysate ( 146.52 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-CNTNAP2 full-length

    Host

    Human

    Theoretical MW (kDa)

    146.52

    Interspecies Antigen Sequence

    Mouse (93)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-CNTNAP2 antibody (H00026047-B01) by Western Blots.

    SDS-PAGE Gel

    CNTNAP2 transfected lysate.

    Western Blot

    Lane 1: CNTNAP2 transfected lysate ( 146.52 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 — CNTNAP2

    Entrez GeneID

    26047

    GeneBank Accession#

    NM_014141.4

    Protein Accession#

    NP_054860.1

    Gene Name

    CNTNAP2

    Gene Alias

    AUTS15, CASPR2, CDFE, DKFZp781D1846, NRXN4

    Gene Description

    contactin associated protein-like 2

    Omim ID

    604569 610042

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons and associated with potassium channels. It may play a role in the local differentiation of the axon into distinct functional subdomains. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It may represent a positional candidate gene for the DFNB13 form of nonsyndromic deafness. [provided by RefSeq

    Other Designations

    cell recognition molecule Caspr2|contactin-associated protein 2|homolog of Drosophila neurexin IV

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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