GJB3 HEK293 Cell Transient Overexpression Lysate(Non-Denatured)

Catalog # L097T6

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Size:100 ug
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
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Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

GJB3 transfected lysate

Western Blot
QC Test

Western Blot

Lane 1: GJB3 transfected lysate ( 31 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    HEK293

    Plasmid

    pCMV-GJB3 full length

    Host

    Human

    Theoretical MW (kDa)

    31

    Lysis Buffer

    Modified RIPA Lysis Buffer:50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

    Concentration

    2 mg/ml

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-GJB3 antibody (H00002707-M01) by Western Blots.

    SDS-PAGE Gel

    GJB3 transfected lysate

    Western Blot

    Lane 1: GJB3 transfected lysate ( 31 KDa).
    Lane 2: Non-transfected lysate.

    Recommend Usage

    Use it directly for immuno-precipitation, or heat lysate with SDS gel loading buffer to 95°C for 5 minutes followed by rapid cooling for western blot application. If dissociating conditions are required, add reducing agent prior to heating.

    Storage Buffer

    In modified RIPA Lysis Buffer.

    Storage Instruction

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

  • Applications

    Western Blot

    Immunoprecipitation

  • Gene Info — GJB3

    Entrez GeneID

    2707

    GeneBank Accession#

    BC012918

    Protein Accession#

    AAH12918

    Gene Name

    GJB3

    Gene Alias

    CX31, DFNA2, EKV, FLJ22486, MGC102938

    Gene Description

    gap junction protein, beta 3, 31kDa

    Omim ID

    133200 600101 603324

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq

    Other Designations

    OTTHUMP00000004183|OTTHUMP00000004184|connexin 31

  • Interactome
  • 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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