Every item is shipped based on the best shipping method assessed for the temperature requirements of that specific item. Items are grouped and shipped together whenever
possible, and a separate shipping charge will be included for each shipping method required. Shipping charges listed below are from our US warehouses to the Contiguous US,
Alaska, Hawaii, Canada and Puerto Rico. Shipping charges for countries outside the US and Canada will be determined once order has been received
Please note: We can not ship to PO boxes
Express Blue Ice
Express Dry Ice
Animal Health Prescription Item
SHIPPING METHODS & CHARGES
Ships via FedEx Ground to Contiguous US, Alaska, Canada, Monday through Friday. This method is used for less temperature sensitive items such as lab ware and animal
health products, bulky and/or heavy items
Labware ships FedEx Ground free of charge to the contiguous US
GM3 Synthase Antibody (B-12) is a high quality monoclonal GM3 Synthase antibody (also designated GM3 Synthase antibody) suitable for the detection of the GM3 Synthase protein of mouse, rat and human origin. GM3 Synthase Antibody (B-12) is available as both the non-conjugated anti-GM3 Synthase antibody form, as well as multiple conjugated forms of anti-GM3 Synthase antibody, including agarose, HRP, PE, FITC and multiple Alexa Fluor® conjugates. GM3 Synthase, also known as Sialyltransferase 9 or ST3Gal V, is a Golgi type II transmembrane glycosyltransferase predominantly expressed in brain and placenta. It belongs to the glycosyltransferase family 29 and is involved in the biosynthesis of complex gangliosides. In particular, GM3 Synthase catalyzes the transfer of α sialic acid to the terminal galactose of lactosylceramide to form the ganglioside GM3. GM3 is the simplest ganglioside and it participates in cell differentiation, signal transduction, and modulation of cell proliferation. The synthesis of GM3 by GM3 Synthase is the first major step in the formation of almost all other gangliosides. For this reason, GM3 Synthase acts as a key regulatory enzyme in the biosynthesis of gangliosides. A mutation in the gene encoding GM3 Synthase can lead to the inability to synthesize α- and β-series gangliosides and may result in Amish infantile epilepsy syndrome.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA
LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences