MSX1 (Human) IP-WB Antibody Pair

Catalog # H00004487-PW4

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Size:1 Set
Price: USD $ 607.00
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  • +1-909-264-1399
    +1-909-992-0619
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  • +1-909-992-3401
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Immunoprecipitation of MSX1 transfected lysate using mouse monoclonal anti-MSX1 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-MSX1.

  • 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)

    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

    Immunoprecipitation-Western Blot

  • Gene Info — MSX1

    Entrez GeneID

    4487

    Gene Name

    MSX1

    Gene Alias

    HOX7, HYD1

    Gene Description

    msh homeobox 1

    Omim ID

    106600 142983 189500 608874

    Gene Ontology

    Hyperlink

    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

  • 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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