Rabbit polyclonal antibody raised against synthetic phosphopeptide of RAD9.
Synthetic phosphopeptide (conjugated with KLH) corresponding to residues surrounding S1129 of Saccharomyces cerevisiae RAD9.
This phospho specific polyclonal antibody reacts with phosphorylated pS1260 of yeast Rad9. Reactivity with non-phosphorylated yeast Rad9 is minimal by ELISA and immunoblotting. No reactivity is expected against the human or mouse analogs of RAD9. Cross reactivity may occur with auto-phosphorylated Rad53 kinase.
Quality Control Testing:
Antibody Reactive Against Synthetic Peptide.
Sandwich ELISA (1:5000) The optimal working dilution should be determined by the end user.
In 20 mM KH2PO4, 150 mM NaCl, pH 7.2 (0.01% sodium azide)
Store at 4°C. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing.
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Immunoblotting of RAD9 (phospho S1129) polyclonal antibody (Cat # PAB11309) was used at a 1 : 200 dilution incubated 8 h at room temperature to detect RAD9 by Western blot. Lanes were loaded with 50 ng each of recombinant GST fusion protein containing S. cerevisiae RAD9 (aa 991-1309 ~60 KDa) on a 4-20% Criterion gel for SDS-PAGE as follows : Lane 1 - non-phosphorylated wild type yeast RAD9, Lane 2 - in vitro phosphorylated wild type yeast RAD9, Lane 3 - non-phosphorylated S1129A/S1260A double mutant RAD9, Lane 4 - in vitro phosphorylated S1129A/S1260A double mutant. Phosphorylation of RAD9 was by treatment with ATP and RAD53 kinase. Detection occurred using a 1:5,000 dilution of IRDye™800 conjugated Donkey anti-Rabbit IgG for 1h at room temperature. LICOR's Odyssey® Infrared Imaging System was used to scan and process the image.
DNA damage-dependent checkpoint protein, required for cell-cycle arrest in G1/S, intra-S, and G2/M; transmits checkpoint signal by activating Rad53p and Chk1p; hyperphosphorylated by Mec1p and Tel1p; potential Cdc28p substrate