MSX2 (Human) Matched Antibody Pair

Catalog # H00004488-AP51

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Price

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Size:1 Set
Price: USD $ 607.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the MSX2 293T overexpression lysate (non-denatured).

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human MSX2.

    Reactivity

    Human

    Quality Control Testing

    Standard curve using MSX2 293T overexpression lysate (non-denatured) as an analyte.

    Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the MSX2 293T overexpression lysate (non-denatured).

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: mouse monoclonal anti-MSX2 (100 ug)
    2. Detection antibody: rabbit purified polyclonal anti-MSX2 (50 ug)
    *Reagents are sufficient for at least 3-5 x 96 well plates using recommended protocols.

    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

    ELISA Pair (Transfected lysate)

  • Gene Info — MSX2

    Entrez GeneID

    4488

    Gene Name

    MSX2

    Gene Alias

    CRS2, FPP, HOX8, MSH, PFM, PFM1

    Gene Description

    msh homeobox 2

    Omim ID

    123101 168500 168550 604757

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2. [provided by RefSeq

    Other Designations

    msh homeo box 2|msh homeobox homolog 2

  • 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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