Anti-AP2 gamma/TFAP2C antibody [3B5] (ab110635)
Key features and details
- Mouse monoclonal [3B5] to AP2 gamma/TFAP2C
- Suitable for: IHC-P, WB, ICC/IF
- Reacts with: Mouse, Human
- Isotype: IgG2b
Overview
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Product name
Anti-AP2 gamma/TFAP2C antibody [3B5]
See all AP2 gamma/TFAP2C primary antibodies -
Description
Mouse monoclonal [3B5] to AP2 gamma/TFAP2C -
Host species
Mouse -
Tested Applications & Species
See all applications and species dataApplication Species ICC/IF HumanIHC-P HumanWB Human -
Immunogen
Synthetic peptide corresponding to Human AP2 gamma/TFAP2C (N terminal).
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Positive control
- Purchase matching WB positive control:Recombinant Human AP2 gamma/TFAP2C protein
- WB: PC-7, A431, mouse placenta, and RAW 264.7 cell lysates; ICC/IF: HeLa, MCF-7, and U251 cells; IHC-P: Human breast cancer;
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General notes
This product was previously labelled as AP2 gamma
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing the problem with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation.
One factor contributing to the crisis is the use of antibodies that are not suitable. This can lead to misleading results and the use of incorrect data informing project assumptions and direction. To help address this challenge, we have introduced an application and species grid on our primary antibody datasheets to make it easy to simplify identification of the right antibody for your needs.
Learn more here.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles. -
Storage buffer
Preservative: 0.05% Sodium azide
Constituents: 99.85% PBS, 0.1% BSA -
Concentration information loading...
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Purity
Protein G purified -
Clonality
Monoclonal -
Clone number
3B5 -
Isotype
IgG2b -
Research areas
Images
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Immunofluorescent analysis of AP2 gamma/TFAP2C using ab110635 shows staining in Hela Cells. AP2 gamma/TFAP2C staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab110635 at a dilution of 1:100 over night at 4°C, washed with PBS and incubated with a Goat Anti-Mouse DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
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All lanes : Anti-AP2 gamma/TFAP2C antibody [3B5] (ab110635) at 1/50 dilution
Lane 1 : PC-3 cell lysate
Lane 2 : A431 cell lysate
Lane 3 : Mouse placenta cell lysate
Lane 4 : RAW 264.7 cell lysate
Lysates/proteins at 30 µg per lane.
Secondary
All lanes : Goat anti-Mouse IgG (H+L), HRP conjugate at 1/4000 dilution
Predicted band size: 49 kDa
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Immunohistochemistry was performed on cancer biopsies of deparaffinized Human breast carcinoma tissue. To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1:50 with ab110635 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP, followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
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Immunofluorescent analysis of AP2 gamma/TFAP2C using ab110635 shows staining in U251 Cells. AP2 gamma/TFAP2C staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab110635 at a dilution of 1:100 over night at 4°C, washed with PBS and incubated with a Goat Anti-Mouse DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
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Immunofluorescent analysis of AP2 gamma/TFAP2C using ab110635 shows staining in MCF-7 Cells. AP2 gamma/TFAP2C staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab110635 at a dilution of 1:20 over night at 4°C, washed with PBS and incubated with a Goat Anti-Mouse DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.