PRKAA1 Recombinant Monoclonal Antibody, Cat#RAC08189
Western Blot, Positive WB detected in: HeLa whole cell lysate (30ug), PC-3 whole cell lysate (30ug), Hep-G2 whole cell lysate (30ug), SW620 whole cell lysate (30ug), U937 whole cell lysate (30ug), All lanes: AMPK alpha 1 antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 64 kDa, Observed band size: 64 kDa, Exposure time: 3min
Overlay Peak curve showing jurkat cells stained with RAC08189 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.
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PRKAA1 Recombinant Monoclonal Antibody, Cat#RAC08189 Western Blot, Positive WB detected in: HeLa whole cell lysate (30ug), PC-3 whole cell lysate (30ug), Hep-G2 whole cell lysate (30ug), SW620 whole cell lysate (30ug), U937 whole cell lysate (30ug), All lanes: AMPK alpha 1 antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 64 kDa, Observed band size: 64 kDa, Exposure time: 3min Overlay Peak curve showing jurkat cells stained with RAC08189 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.

PRKAA1 Recombinant Monoclonal Antibody

BiomatikSKU: RAC08189-100ul
Size: 100ul
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Western Blot, Positive WB detected in: HeLa whole cell lysate (30ug), PC-3 whole cell lysate (30ug), Hep-G2 whole cell lysate (30ug), SW620 whole cell lysate (30ug), U937 whole cell lysate (30ug), All lanes: AMPK alpha 1 antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/50000 dilution, Predicted band size: 64 kDa, Observed band size: 64 kDa, Exposure time: 3min
Overlay Peak curve showing jurkat cells stained with RAC08189 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.

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