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Project-Id-Version: POT-Creation-Date: PO-Revision-Date: Last-Translator: Steve Noone Language-Team: MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: 8bit

  • Hh/Gli Antagonist, GANT58
    A cell-permeable tetrapyridinylthiophene compound that acts as downstream Hedgehog (Hh) pathway blocker and targets Gli-mediated gene transactivation (IC50 ~ 5 µM in SAG-stimulated Shh-L2 cells). Shown to reduce cellular mRNA levels of Hh target genes, Gli1, Hip1,& Ptch, and inhibit Gli-dependent tumor growth both in vitro and in vivo. Its action appears to be Hh pathway-selective, downstream of Smo and Sufu, but does not seem to interfere with Gli DNA binding.
    Katalog #CAS NummerSummenformelMenge
    sc-221723n.n.C24H16N4S5 mg
  • Cyclopamine-KAAD
    A potent, cell-permeable analog of Cyclopamine that specifically inhibits the Hedgehog (Hh) signaling with similar or lower toxicity. Binds to SmoA1 and promotes its exit from the endoplasmic reticulum. Suppresses both the ShhNp-induced pathway activity and SmoA1-induced reporter activity.
    Katalog #CAS NummerSummenformelMenge
    sc-221448306387-90-6C44H63N3O4100 µg
  • Despiro Cyclopamine
    An analogue of Cyclopamine, a sonic hedgehog inhibitor.
    Katalog #CAS NummerSummenformelMenge
    sc-218162n.n.C27H41NO21 mg
  • Veratramine, HCl, V. californicum
    This compound is a cell-permeable steroidal alkaloid that is structurally related to and is reported to serve as a suitable inactive control for Cyclopamine, Cyclopamine-KAAD (sc-221448), and Jervine in Shh (sonic hedgehog) signaling studies.
    Katalog #CAS NummerSummenformelMenge
    sc-3561911258005-82-1C27H39NO2•HCl5 mg