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Western Blot Positive WB detected in: 3 different overexpression lysates with HA tagged All lanes: HA-Tag antibody at 1:1000 Secondary Goat polyclonal to Mouse IgG at 1/10000 dilution Predicted band size: 35, 35, 48 kDa Observed band size: 35, 35, 48 kDa

Overlay histogram showing 293F transfected whole cell stained with CSB-MA000141M0m (red line) at 1:100. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.

Western Blot Positive WB detected in: HA-tagged fusion protein at 50ng, 25ng, 12.5ng, 6.25ng, 3.125ng, 1.5625ng All lanes: HA-Tag antibody at 1:1000 Secondary Goat polyclonal to Mouse IgG at 1/10000 dilution Predicted band size: 35 kDa Observed band size: 35 kDa

Western Blot Positive WB detected in: HA-tagged fusion protein All lanes: HA-Tag antibody at 1:5000, 1:10000, 1:20000, 1:40000, 1:80000, 1:160000 Secondary Goat polyclonal to Mouse IgG at 1/10000 dilution Predicted band size: 35 kDa Observed band size: 35 kDa

Western Blot Positive WB detected in: 6 different recombinant proteins with HA tagged, Hela whole cell lysate, 3T3 whole cell lysate All lanes: HA-Tag antibody at 1:1000 Secondary Goat polyclonal to Mouse IgG at 1/10000 dilution

Immunofluorescence staining of 293F cells with CSB-MA000141M0m at 1:100, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).

Immunofluorescence staining of 293F transfected cells with CSB-MA000141M0m at 1:100, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).

Immunofluorescence staining of 293F cells and 293F transfected cells with Company A, Company B, Company C, Company D, Company E, CSB-MA000141M0m at 1:100, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).

Immunoprecipitating HA-Tag in 293F transfected whole cell lysate Lane 1: Mouse control IgG (1microg) instead of CSB-MA000141M0m in 293F transfected whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000) Lane 2: CSB-MA009476A0m (5microg) + 293F transfected whole cell lysate (500microg) Lane 3: 293F transfected whole cell lysate (20microg)

Immunoprecipitating HA-Tag in 293F transfected whole cell lysate Lane 1: Mouse control IgG (1microg) instead of CSB-MA000141M0m in 293F transfected whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000) Lane 2: Company A (5microg), Company B (5microg),Company C (5microg),Company D (5microg),Company E (5microg),CSB-MA009476A0m (5microg) + 293F transfected whole cell lysate (500microg) Lane 3: 293F transfected whole cell lysate (20microg)

HA-Tag Monoclonal Antibody is validated for ELISA, FC, IF, IP, WB & tested in All Species. Cusabio is available at Bio-Connect

HA-Tag Monoclonal Antibody antibody | CSB-MA000141M0M | Cusabio

HA-Tag Monoclonal Antibody

Assembles with the antigen receptor of B-lymphocytes in order to decrease the threshold for antigen receptor-dependent stimulation.

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HA-Tag Monoclonal Antibody

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