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Your Position: ホーム > Protein > Cadherin-17 > CA7-H52A9

Human Cadherin-17 / CDH17 Protein, Mouse IgG1 Fc Tag

  • Synonym
    Cadherin-17,CDH17,HPT-1, LI-cadherin
  • Source
    Human Cadherin-17 Protein, Mouse IgG1 Fc Tag(CA7-H52A9) is expressed from human 293 cells (HEK293). It contains AA Gln 23 - Met 787 (Accession # Q12864-1).
    Predicted N-terminus: Gln 23
  • Molecular Characterization
    Cadherin-17 Structure

    This protein carries a mouse IgG1 Fc tag at the C-terminus

    The protein has a calculated MW of 111.2 kDa. The protein migrates as 130-135 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.

  • Endotoxin
    Less than 1.0 EU per μg by the LAL method.
  • Purity

    >90% as determined by SDS-PAGE.

  • Formulation

    Lyophilized from 0.22 μm filtered solution in 20 mM Tris, 150 mM NaCl, pH8.0 with trehalose as protectant.

    Contact us for customized product form or formulation.

  • Reconstitution

    Please see Certificate of Analysis for specific instructions.

    For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

  • Storage

    For long term storage, the product should be stored at lyophilized state at -20°C or lower.

    Please avoid repeated freeze-thaw cycles.

    This product is stable after storage at:

    1. -20°C to -70°C for 12 months in lyophilized state;
    2. -70°C for 3 months under sterile conditions after reconstitution.
SDS-PAGE
Cadherin-17 SDS-PAGE

Human Cadherin-17 Protein, Mouse IgG1 Fc Tag on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%.

Bioactivity-ELISA
 Cadherin-17 ELISA

Immobilized Human Cadherin-17 Protein, Mouse IgG1 Fc Tag (Cat. No. CA7-H52A9) at 1 μg/mL (100 μL/well) can bind Human Anti-Cadherin 17 with a linear range of 0.5-31 ng/mL (QC tested).

  • Background
    Cadherin-17, also known as liver-intestine (LI) Cadherin, belongs to the cadherin family of calcium-dependent cell adhesion molecules. In vivo studies showed CDH17 knockout resulted in apoptotic PC tumor death through activating caspase-3 activity. Taken together, CDH17 functions as an oncogenic molecule critical to PC growth by regulating tumor apoptosis signaling pathways and CDH17 could be targeted to develop an anti-PC therapeutic approach.
  • Clinical and Translational Updates

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