WHSC1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00007468-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

WHSC1 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: WHSC1 transfected lysate ( 71.28 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-WHSC1 full-length

    Host

    Human

    Theoretical MW (kDa)

    71.28

    Interspecies Antigen Sequence

    Mouse (86); Rat (85)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-WHSC1 antibody (H00007468-B01) by Western Blots.

    SDS-PAGE Gel

    WHSC1 transfected lysate.

    Western Blot

    Lane 1: WHSC1 transfected lysate ( 71.28 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 — WHSC1

    Entrez GeneID

    7468

    GeneBank Accession#

    NM_133334.2

    Protein Accession#

    NP_579889.1

    Gene Name

    WHSC1

    Gene Alias

    FLJ23286, KIAA1090, MGC176638, MMSET, NSD2, REIIBP, TRX5, WHS

    Gene Description

    Wolf-Hirschhorn syndrome candidate 1

    Omim ID

    602952

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq

    Other Designations

    IL5 promoter REII region-binding protein|OTTHUMP00000149955|OTTHUMP00000159146|Wolf-Hirschhorn syndrome candidate 1 protein|multiple myeloma SET domain containing protein type III|trithorax/ash1-related protein 5

  • 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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