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Anti-CBP (Acetyl-K1535) Antibody

Catalog Number: orb256470

DispatchUsually dispatched within 5-10 working days
$ 160.00
Catalog Numberorb256470
CategoryAntibodies
DescriptionRabbit polyclonal antibody to CBP
TargetCREBBP
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityHuman, Mouse, Rat
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
PurificationThe antibody was purified by immunogen affinity chromatography.
ImmunogenKLH-conjugated synthetic acetylated peptide corresponding to residues surrounding K1535 of human CBP protein. The exact sequence is proprietary.
UniProt IDQ92793, P45481, Q6JHU9
Tested applicationsIF, IH, WB
Dilution rangeWB: 1:500-1000, IHC-P: 1:100-200, IF/ICC: 1:100-500
Antibody TypePrimary Antibody
SourceRabbit
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Alternative namesanti CBP antibody, anti CREB-binding protein antib
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NoteFor research use only
Entrez1387
Anti-CBP (Acetyl-K1535) Antibody

Western blot analysis of CBP (Acetyl-K1535) expression in HeLa (A), NIH3T3 (B) whole cell lysates. (Predicted band size: 265 kD; Observed band size: 265 kD)

Anti-CBP (Acetyl-K1535) Antibody

Immunohistochemical analysis of CBP (Acetyl-K1535) staining in human lung cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Anti-CBP (Acetyl-K1535) Antibody

Immunofluorescent analysis of CBP (Acetyl-K1535) staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.