This product is an antibody that recognizes HER2. The antibody 2D9 can be used for immunoassay techniques such as: ELISA, FC.
Figure 1 Epitope mapping of anti-HER2 antibodies using indirect immunofluorescence assay.
Trastuzumab, CB11: a monoclonal antibody recognizing an epitope at intracellular domain of HER2 that was used as a positive control for expression of transfected plasmids.
Ceran, C., Cokol, M., Cingoz, S., Tasan, I., Ozturk, M., & Yagci, T. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC cancer, 12(1), 450.
Figure 2 In vitro molecular responses of SK-BR-3 cell to anti-HER2 antibody.
Untreated cells were incubated in a parallel experiment in the absence of any treatment.
Ceran, C., Cokol, M., Cingoz, S., Tasan, I., Ozturk, M., & Yagci, T. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC cancer, 12(1), 450.
Figure 3 Binding affinities of anti-HER2 antibodies.
HER2 ECD ELISA assay showing the binding strengths of five monoclonal antibodies. HER2 ECD-coated plates were incubated with increasing concentrations of anti-HER2 antibodies, followed by alkaline phosphatase-conjugated anti-mouse IgG antibodies.
Ceran, C., Cokol, M., Cingoz, S., Tasan, I., Ozturk, M., & Yagci, T. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC cancer, 12(1), 450.
Figure 4 Flow cytometric analysis of antibody binding to high HER2-expressing BT-474.
Fixed single-cell suspensions were incubated with anti-HER2 antibodies, followed by Alexa-488-conjugated secondary antibodies and fluorescence intensities were measured using flow cytometry.
Ceran, C., Cokol, M., Cingoz, S., Tasan, I., Ozturk, M., & Yagci, T. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC cancer, 12(1), 450.
Figure 5 Anti-HER2 antibodies exhibit enhanced anti-growth effect in the presence of tumor necrosis factor-α in SK-BR-3 cells.
SK-BR-3 cells were plated onto 96-well plates and incubated at 37°C with 5% CO2. After 2 h of incubation, antibodies (0–10 μg/ml) were added, and cells were incubated for 6 days.
Ceran, C., Cokol, M., Cingoz, S., Tasan, I., Ozturk, M., & Yagci, T. (2012). Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α. BMC cancer, 12(1), 450.
This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:
• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production
See more details about Hi-Affi™ recombinant antibody benefits.
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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.
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