QPCTL Antibody (D-3) is a mouse monoclonal IgG1 (kappa light chain) provided at 200 µg/ml
raised against amino acids 276-325 mapping near the C-terminus of QPCTL of human origin
recommended for detection of QPCTL of mouse, rat and human origin by WB, IP, IF and ELISA
m-IgG Fc BP-HRP, m-IgG1 BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for QPCTL Antibody (D-3) for WB applications. These reagents are now offered in bundles with QPCTL Antibody (D-3) (see ordering information below).
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
QPCTL (glutaminyl-peptide cyclotransferase-like protein) is a 382 amino acid single-pass membrane protein that belongs to the glutaminyl-peptide cyclotransferase family. The QPCTL protein binds one zinc ion per subunit. The QPCTL gene is conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, S.cerevisiae, K.lactis, E.gossypii, M.grisea and N.crassa, and maps to human chromosome 19q13.32.Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
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