MSX1 monoclonal antibody, clone 5D11

Catalog # MAB10816

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Price

Stock

Quantity

Size:100 uL
Price: USD $ 531.00
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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
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis using MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816) against NTERA-2 cell lysate.

Enzyme-linked Immunoabsorbent Assay
Application

Enzyme-linked Immunoabsorbent Assay

ELISA measurement of MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against partial recombinant MSX1.

    Immunogen

    Recombinant protein corresponding to human MSX1.

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Isotype

    IgG1

    Recommend Usage

    ELISA (1:10000)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In ascites (0.03% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Cell lysate)

    Western blot analysis using MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816) against NTERA-2 cell lysate.

    Enzyme-linked Immunoabsorbent Assay

    ELISA measurement of MSX1 monoclonal antibody, clone 5D11 (Cat # MAB10816).
  • 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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