FBXW4 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00006468-T01

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Size:100 uL
Price: USD $ 247.00
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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

FBXW4 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: FBXW4 transfected lysate ( 45.43 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-FBXW4 full-length

    Host

    Human

    Theoretical MW (kDa)

    45.43

    Interspecies Antigen Sequence

    Mouse (93); Rat (94)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-FBXW4 antibody (H00006468-B01) by Western Blots.

    SDS-PAGE Gel

    FBXW4 transfected lysate.

    Western Blot

    Lane 1: FBXW4 transfected lysate ( 45.43 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 — FBXW4

    Entrez GeneID

    6468

    GeneBank Accession#

    NM_022039

    Protein Accession#

    NP_071322

    Gene Name

    FBXW4

    Gene Alias

    DAC, FBW4, FBWD4, SHFM3, SHSF3

    Gene Description

    F-box and WD repeat domain containing 4

    Omim ID

    600095 608071

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22. [provided by RefSeq

    Other Designations

    F-box and WD-40 domain protein 4|F-box/WD repeat protein 4|OTTHUMP00000059175|dactylin

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