Mouse Recombinant Monoclonal Fas antibody. Carrier free. Suitable for Flow Cyt and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ICC | IP | Flow Cyt | WB | |
---|---|---|---|---|
Human | Not recommended | Not recommended | Tested | Not recommended |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended |
Rat | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
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Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human | Dilution info - | Notes - |
Receptor for TNFSF6/FASLG. The adapter molecule FADD recruits caspase CASP8 to the activated receptor. The resulting death-inducing signaling complex (DISC) performs CASP8 proteolytic activation which initiates the subsequent cascade of caspases (aspartate-specific cysteine proteases) mediating apoptosis. FAS-mediated apoptosis may have a role in the induction of peripheral tolerance, in the antigen-stimulated suicide of mature T-cells, or both. The secreted isoforms 2 to 6 block apoptosis (in vitro).
CD95, APT1, FAS1, TNFRSF6, FAS, Tumor necrosis factor receptor superfamily member 6, Apo-1 antigen, Apoptosis-mediating surface antigen FAS, FASLG receptor
Mouse Recombinant Monoclonal Fas antibody. Carrier free. Suitable for Flow Cyt and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
This antibody is a carrier free version of Recombinant mouse CSF3 protein (Active) ab287913.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Fas antibody [LOB3/17] ab289713, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of K-562 (Human chronic myelogenous leukemia lymphoblast, Left) / Raji(Human Burkitt's lymphoma B lymphocyte, Right) cells labeling Fas with Anti-Fas antibody [LOB3/17] ab289713 at 1/1000 dilution (Red) compared with a Mouse monoclonal IgG (Black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Mouse IgG (Alexa Fluor® 647, Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119), at 1/2000 dilution was used as the secondary antibody.
Negative control: K-562.
Gated on viable cells.
This data was developed using Anti-Fas antibody [LOB3/17] ab289713, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of human peripheral blood mononuclear cell (PBMC) cells labeling Fas with Anti-Fas antibody [LOB3/17] ab289713 at 1/1000 dilution (right), compared with a Mouse monoclonal IgG (left). Secondary antibody details Goat Anti-Mouse IgG (Alexa Fluor® 488, Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113), at 1/2000 dilution was used as the secondary antibody.
Gated on viable cells.
This data was developed using Anti-Fas antibody [LOB3/17] ab289713, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Jurkat (Human T cell leukemia T lymphocyte) cells labeling Fas with Anti-Fas antibody [LOB3/17] ab289713 at 1/1000 dilution (Red) compared with a Mouse monoclonal IgG (Black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Secondary antibody details Goat Anti-Mouse IgG (Alexa Fluor® 647, Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) preadsorbed ab150119), at 1/2000 dilution was used as the secondary antibody.
Gated on viable cells.
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