Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5) Peptide

ST3GAL5 Reactivity: Mammalian Host: Synthetic BP, IHC, WB
Catalog No. ABIN937546
  • Target See all ST3GAL5 products
    ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Sequence
    DSEAESKYDP PFGFRKFSSK VQTLLELLPE HDLPEHLKAK TCRRCVVIGS
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of ST3 GAL5 antibody,
    Alternative Names: ST3GAL5 control peptide, ST3GAL5 antibody Blocking Peptide, Anti-ST3GAL5 Blocking Peptide, St3 Beta-Galactoside Alpha-23-Sialyltransferase 5 Blocking Peptide, SIAT9 Blocking Peptide, SIATGM3S Blocking Peptide, ST3GalV Blocking Peptide, ST3GAL5, STGAL5-3, STGAL5 3, STGAL5-3 Blocking Peptide, STGAL5 3 Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
    Background
    Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. ST3GAL5 is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. It is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in its gene has been associated with Amish infantile epilepsy syndrome.
    Molecular Weight
    48 kDa
You are here:
Support