MSX1 monoclonal antibody (M04), clone 3A8

Catalog # H00004487-M04

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Size:100 ug
Price: USD $ 335.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Immunoprecipitation
Application

Immunoprecipitation

Immunoprecipitation of MSX1 transfected lysate using anti-MSX1 monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with MSX1 MaxPab rabbit polyclonal antibody.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a full length recombinant MSX1.

    Immunogen

    MSX1 (NP_002439, 216 a.a. ~ 297 a.a) full length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    NRRAKAKRLQEAELEKLKMAAKPMLPPAAFGLSFPLGGPAAVAAAAGASLYGASGPFQRAALPVAPVGLYTAHVGYSMYHLT

    Host

    Mouse

    Reactivity

    Human

    Isotype

    IgG2a Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Immunoprecipitation

    Immunoprecipitation of MSX1 transfected lysate using anti-MSX1 monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with MSX1 MaxPab rabbit polyclonal antibody.

    ELISA

  • Gene Info — MSX1

    Entrez GeneID

    4487

    GeneBank Accession#

    NM_002448

    Protein Accession#

    NP_002439

    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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