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Anti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal Antibody

Catalog Number: orb548611

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Catalog Numberorb548611
CategoryAntibodies
DescriptionAnti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal Antibody
ClonalityMonoclonal
Species/HostRabbit
IsotypeRabbit IgG
ConjugationUnconjugated
ReactivityHuman
Form/AppearanceLiquid
ConcentrationActual concentration vary by lot. Use suggested dilution ratio to decide dilution procedure.
ImmunogenA synthesized peptide derived from human Phospho-DNA PKcs (S2056)
UniProt IDP78527
MW185 kDa
Tested applicationsICC, IF, IHC, WB
Application notesWB 1:500-1:2000IHC 1:50-1:200ICC/IF 1:50-1:200
Antibody TypePrimary Antibody
Clone NumberBOD-16
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 namesDNA-dependent protein kinase catalytic subunit; DN
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NoteFor research use only
Anti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal Antibody

Western blot analysis of Phospho-DNA PKcs (Ser2056) expression in alkaline treated Jurkat cell lysate.

Anti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal Antibody

Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-Phospho-DNA PKcs (S2056) antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Anti-Phospho-DNA PKcs (S2056) PRKDC Rabbit Monoclonal Antibody

Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue using anti-Phospho-DNA PKcs (S2056) antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.