PAX6 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00005080-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

PAX6 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: PAX6 transfected lysate ( 46.53 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-PAX6 full-length

    Host

    Human

    Theoretical MW (kDa)

    46.53

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-PAX6 antibody (H00005080-B01) by Western Blots.

    SDS-PAGE Gel

    PAX6 transfected lysate.

    Western Blot

    Lane 1: PAX6 transfected lysate ( 46.53 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 — PAX6

    Entrez GeneID

    5080

    GeneBank Accession#

    NM_000280.2

    Protein Accession#

    -

    Gene Name

    PAX6

    Gene Alias

    AN, AN2, D11S812E, MGC17209, MGDA, WAGR

    Gene Description

    paired box 6

    Omim ID

    106210 120200 120430 129750 136520 148190 165550 603807 607108

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes paired box gene 6, one of many human homologs of the Drosophila melanogaster gene prd. In addition to the hallmark feature of this gene family, a conserved paired box domain, the encoded protein also contains a homeo box domain. Both domains are known to bind DNA, and function as regulators of gene transcription. This gene is expressed in the developing nervous system, and in developing eyes. Mutations in this gene are known to cause ocular disorders such as aniridia and Peter's anomaly. Alternatively spliced transcript variants encoding either the same or different isoform have been found for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000038833|OTTHUMP00000038834|OTTHUMP00000038835|OTTHUMP00000038836|OTTHUMP00000038837|OTTHUMP00000038838|OTTHUMP00000038839|OTTHUMP00000038840|paired box gene 6|paired box homeotic gene-6

  • Interactome
  • Pathway
  • 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