Anti-MSANTD2 Antibody (B-8) is a mouse monoclonal IgM (kappa light chain) MSANTD2 antibody provided at 200 µg/ml
specific for an epitope mapping between amino acids 237-271 within an internal region of MSANTD2 of human origin
recommended for detection of MSANTD2 of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including and canine, bovine and porcine; non cross-reactive with other C11orf family members
blocking peptide, sc-390361 P
Contact our Technical Service Department (or your local Distributor) for more information on how to receive a FREE 10 µg sample of MSANTD2 (B-8): sc-390361.
See m-IgGκ BP-HRP (mouse IgGκ binding protein-HRP), our highly recommended recombinant alternative to conventional secondary anti-mouse IgG reagents.
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
MSANTD2 Antibody (B-8) is a high quality monoclonal MSANTD2 antibody (also designated MSANTD2 antibody) suitable for the detection of the MSANTD2 protein of mouse, rat and human origin. MSANTD2 Antibody (B-8) is available as the non-conjugated anti-MSANTD2 antibody. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association-dense chromosome. The chromosome 11-encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia telangiectasia. The blood disorders sickle cell anemia and b thalasse-mia are caused by HBB gene mutations. Wilms′ tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.