- Flow Cyt
Supplier Data
Flow Cytometry - Anti-IL17A antibody [EPR19941-88R] (AB323803)
Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized Isotype (Left) / 293T (human embryonic kidney epithelial cell) cells transfected with a human IL17A expression vector containing a Myc tag (Middle) / 293T cells transfected with an empty expression vector containing a Myc tag (Right) cells labelling IL17A with ab323803 at 1/5000 dilution (0.01 ug) / Middle and Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-IL17A antibody [EPR19941-88R] (AB323803)
Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized Untreated human PBMC (Human peripheral blood mononuclear cell) (upper left and upper right) / Human PBMC treated with cell stimulation cocktail for 6 hours (down left and down right) cells labelling IL17A with ab323803 at 1/500 dilution (0.1 ug) / upper right and down right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Human PBMC were co-stained with anti human CD19 conjugated to Alexa Fluor®647.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-IL17A antibody [EPR19941-88R] (AB323803)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Human PBMC (Human primary peripheral blood mononuclear cell) cells labelling IL17A with ab323803 at 1/100 (4.96 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green).
Confocal image showing cytoplasmic staining in subsets of human PBMC treated with cell stimulation cocktail for 6 hours (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-human CD4 mouse monoclonal antibody (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-IL17A antibody [EPR19941-88R] (AB323803)
Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized Untreated human PBMC (Human peripheral blood mononuclear cell) (upper left and upper right) / Human PBMC treated with cell stimulation cocktail for 6 hours (down left and down right) cells labelling IL17A with ab323803 at 1/500 dilution (0.1 ug) / upper right and down right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Human PBMC were co-stained with anti human CD4 conjugated to BV421.
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제품 세부 정보
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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