PRAM1 antibody was purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Immunogen
PRAM1 antibody was raised against a 15 amino acid synthetic peptide near the C-Terminus of PRAM1.
ELISA: Antibody detection limit dilution 1:8000. Western Blot: Approximately 90-100 kDa band seen in Jurkat cell lysates. Recommended for use at 1-3 μg/mL. Overnight incubation is recommended with this antibody. Please note that although the predicted MW of PRAM-1 is 79 kDa, Moog-Lutz et al., (J. Biol. Chem, Jun 2001, 276: 22375 - 22381) detected aPRAM-1 migrating with an apparent molecular mass of 97 kDa and this is what we observed as well.
Restrictions
For Research Use only
Format
Liquid
Concentration
500 μg/mL
Buffer
Tris saline, 0.02 % sodium azide, pH 7.3 with 0.5 % bovine serum albumin.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.