Product Browser

Last updated: 2016/12/4

Product Compare

Product Compare Cancel Click this icon to add products to compare list. Select up to 10 products.

Quick Order (Tutorial)

Input Catalog #,
place order here!
Catalog # :
  • Where to buy
  • Choose your location

MSX1 (Human) IP-WB Antibody Pair

  • Catalog # : H00004487-PW5
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Immunoprecipitation-Western Blot (IP-WB)

    QC Testing of H00004487-PW5
    Immunoprecipitation of MSX1 transfected lysate using mouse monoclonal anti-MSX1 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-MSX1.
  • Supplied Product:
  • Antibody pair set content:
    1. Antibody pair for IP: mouse monoclonal anti-MSX1 (300 ug)
    2. Antibody pair for WB: rabbit polyclonal anti-MSX1 (50 ul)
  • Storage Instruction:
  • Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
  • Applications
  • Application Image
  • Immunoprecipitation-Western Blot
  • Gene Information
  • Entrez GeneID:
  • 4487
  • Gene Name:
  • MSX1
  • Gene Alias:
  • HOX7,HYD1
  • Gene Description:
  • msh homeobox 1
  • Gene Summary:
  • This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000115387,homeobox 7,msh homeo box 1,msh homeobox homolog 1
  • RSS
  • YouTube
  • Linkedin
  • Facebook