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WB analysis of SHH(AA: 26-161)-hIgGFc transfected HEK293 cell lysate using GTX83231 Shh antibody [8G3].
WB analysis of SHH(AA: 26-161)-hIgGFc transfected HEK293 cell lysate using GTX83231 Shh antibody [8G3].
WB analysis of SHH(AA: 26-161)-hIgGFc transfected HEK293 cell lysate using GTX83231 Shh antibody [8G3].

Shh antibody [8G3]

GTX83231
GeneTex
ApplicationsWestern Blot, ELISA
Product group Antibodies
TargetSHH
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Overview

  • Supplier
    GeneTex
  • Product Name
    Shh antibody [8G3]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1/500 - 1/2000. ELISA: 1/10000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    8G3
  • Conjugate
    Unconjugated
  • Gene ID6469
  • Target name
    SHH
  • Target description
    sonic hedgehog signaling molecule
  • Target synonyms
    HHG1; HLP3; HPE3; MCOPCB5; shh unprocessed N-terminal signaling and C-terminal autoprocessing domains; ShhNC; SMMCI; sonic hedgehog homolog; sonic hedgehog protein; TPT; TPTPS
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDQ15465
  • Protein Name
    Sonic hedgehog protein
  • Scientific Description
    This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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