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Anti-Caldesmon (Phospho-S789) Antibody

Catalog Number: orb338958

DispatchUsually dispatched within 5-10 working days
$ 190.00
Catalog Numberorb338958
CategoryAntibodies
DescriptionRabbit polyclonal antibody to CALD1
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, WB
ReactivityHuman, Mouse, Rat
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S789 of human Caldesmon protein. The exact sequence is proprietary.
Antibody TypePrimary Antibody
Dilution rangeWB: 1:500-1000, IHC-P: 1:100-200, IF/ICC: 1:100-500
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetCALD1
Entrez25687, 800
UniProt IDQ62736, Q05682
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.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti CAD antibody, anti CDM antibody, anti Caldesm
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-Caldesmon (Phospho-S789) Antibody

Western blot analysis of Caldesmon (Phospho-S789) expression in HEK293T PMA-treated (A), NIH3T3 (B) whole cell lysates. (Predicted band size: 93 kD; Observed band size: 80 kD)

Anti-Caldesmon (Phospho-S789) Antibody

Immunohistochemical analysis of Caldesmon (Phospho-S789) staining in human brain formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (Phospho-H 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-Caldesmon (Phospho-S789) Antibody

Immunofluorescent analysis of Caldesmon (Phospho-S789) 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. DAPI was used to stain the cell nuclei (blue).