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Anti-CSNK2A1 Antibody EP1963Y
Also for CSNK2A1 (NM_177560)
|A synthetic peptide corresponding to residues near the N-terminal of human CKII protein was used as an immunogen.|
|Mouse, Rat, Human
||Lot dependent; please refer to CoA along with shipment
|WB, IHC, FC
||WB: 1:500 - 1:1000; FC: 1:20 - 1:50; IHC-P: Use at an assay dependent concentration
|PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%|
|Tissue culture supernatant
|Is unsuitable for ICC or IP.
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Western blot - CKII alpha antibody [EP1963Y]; Anti-CKII alpha antibody [EP1963Y] at 1/1000 dilution + HeLa cell lysate at 10 ug.Secondary.HRP labelled goat anti-rabbit at 1/2000 dilution.Predicted band size : 45 kDa.Observed band size : 45 kDa.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - CKII alpha antibody [EP1963Y]; Immunohistochemical analysis of CKII alpha in paraffin embedded human breast carcinoma tissue using TA303470 at a 1/50 dilution.
Flow Cytometry - Anti-CKII alpha antibody [EP1963Y]; Overlay histogram showing Jurkat cells stained with TA303470 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody for 30 min at 22°C. The secondary antibody used was Alexa Fluor 488 goat anti-rabbit IgG (H&L) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1ug/1x10^6 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.