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
α-1-Microglobulin Antibody (10A12) is a high quality monoclonal alpha-1-Microglobulin antibody (also designated α-1-Microglobulin antibody) suitable for the detection of the alpha-1-Microglobulin protein of human origin. α-1-Microglobulin Antibody (10A12) is available as the non-conjugated anti-alpha-1-Microglobulin antibody. AMBP (alpha-1-microglobulin/bikunin precursor) is a 352 amino acid protein that is proteolytically cleaved to produce three active peptides, designated α-1-Microglobulin, Bikunin and ITI-LC (inter-α-trypsin light chain). α-1-Microglobulin, also known as protein HC, is a 184 amino acid secreted peptide that exists as a monomer and is present in many physiological fluids, including urine, plasma and cerebrospinal fluid. Interacting with Fibronectin, α-1-Microglobulin belongs to the lipocalin family of transport proteins and may participate in the regulation of inflammatory processes, as well as in the autocatalytic creation of chromophores. The gene encoding the AMBP precursor maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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To place an order using RMB or to ship to mainland China, please visit www.scbio.cn