Mouse Fibroblast Activation Protein alpha /FAP Antibody
R&D Systems | Catalog # MAB9727
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Leu26-Asp761
Accession # P97321
Specificity
Clonality
Host
Isotype
Scientific Data Images for Mouse Fibroblast Activation Protein alpha /FAP Antibody
Detection of Fibroblast Activation Protein alpha/FAP in C2C12 Mouse Cell Line by Flow Cytometry.
C2C12 mouse myoblast cell line was stained with Rat Anti-Mouse Fibroblast Activation Protein alpha/FAP Monoclonal Antibody (Catalog # MAB9727, filled histogram) or isotype control antibody (Catalog # MAB005, open histogram), followed by Phycoerythrin-conjugated Anti-Rat IgG Secondary Antibody (Catalog # F0105B). View our protocol for Staining Membrane-associated Proteins.Fibroblast Activation Protein alpha /FAP in C2C12 Mouse Cell Line.
Fibroblast Activation Protein a/FAP was detected in immersion fixed C2C12 mouse myoblast cell line using Rat Anti-Mouse Fibroblast Activation Protein a/FAP Monoclonal Antibody (Catalog # MAB9727) at 8 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Rat IgG Secondary Antibody (red; Catalog # NL013) and counterstained with DAPI (blue). Specific staining was localized to plasma membrane and cytoplasm. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.Detection of Fibroblast Activation Protein alpha/FAP in NIH-3T3 Mouse Embryonic Fibroblast Cell Line by Flow Cytometry.
Used 3uL for 15mins at 4°C on 3T3 cells transduced to over express murine FAP. Image from a verified customer review.Detection of Fibroblast Activation Protein alpha /FAP by Western Blot
FAP expression is up-regulated in the myocardium of isoproterenol (ISO) mice and in cardiac fibroblasts upon TGF-beta 1 stimulation. (A) Quantitative polymerase chain reaction (qPCR) analysis showing messenger RNA (mRNA) expression levels of Col1 alpha 1, Acta2, and FAP in heart tissue from ISO-treated mice. n = 6. Data are presented as mean ± SEM. **P < 0.01; ****P < 0.0001. (B) Western blotting analysis of Col1 alpha 1, alpha -smooth muscle actin ( alpha -SMA), and FAP protein expressions in the hearts of mice treated with ISO or saline. (C) Sirius Red staining and immunohistochemical staining for FAP in hearts from ISO-treated mice. (D) mRNA expression levels of Col1 alpha 1, Acta2, and FAP in neonatal rat cardiac fibroblasts (NRCFs) treated with TGF-beta 1 (10 ng/ml) for 24 h, assessed by qPCR. (E) Western blotting analysis of FAP protein expression in NRCFs after TGF-beta 1 treatment. (F) Flow cytometry analysis of FAP protein expression in NRCFs following TGF-beta 1 treatment. (G) Immunofluorescence (IF) analysis of FAP protein expression in NRCFs post-TGF-beta 1 treatment. IHC, immunohistochemical; Col I, type I collagen; PBS, phosphate-buffered saline; Ctrl, control; GAPDH, glyceraldehyde-3-phosphate; DAPI, 4′,6-diamidino-2-phenylindole. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/40225952), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Fibroblast Activation Protein alpha /FAP by Western Blot
FAP expression is up-regulated in the myocardium of isoproterenol (ISO) mice and in cardiac fibroblasts upon TGF-beta 1 stimulation. (A) Quantitative polymerase chain reaction (qPCR) analysis showing messenger RNA (mRNA) expression levels of Col1 alpha 1, Acta2, and FAP in heart tissue from ISO-treated mice. n = 6. Data are presented as mean ± SEM. **P < 0.01; ****P < 0.0001. (B) Western blotting analysis of Col1 alpha 1, alpha -smooth muscle actin ( alpha -SMA), and FAP protein expressions in the hearts of mice treated with ISO or saline. (C) Sirius Red staining and immunohistochemical staining for FAP in hearts from ISO-treated mice. (D) mRNA expression levels of Col1 alpha 1, Acta2, and FAP in neonatal rat cardiac fibroblasts (NRCFs) treated with TGF-beta 1 (10 ng/ml) for 24 h, assessed by qPCR. (E) Western blotting analysis of FAP protein expression in NRCFs after TGF-beta 1 treatment. (F) Flow cytometry analysis of FAP protein expression in NRCFs following TGF-beta 1 treatment. (G) Immunofluorescence (IF) analysis of FAP protein expression in NRCFs post-TGF-beta 1 treatment. IHC, immunohistochemical; Col I, type I collagen; PBS, phosphate-buffered saline; Ctrl, control; GAPDH, glyceraldehyde-3-phosphate; DAPI, 4′,6-diamidino-2-phenylindole. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/40225952), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse Fibroblast Activation Protein alpha /FAP Antibody
ELISA
This antibody functions as an ELISA capture antibody when paired with Rat Anti-Mouse Fibroblast Activation Protein alpha /FAP Monoclonal Antibody (Catalog # MAB97271).
This product is intended for assay development on various assay platforms requiring antibody pairs.
Flow Cytometry
Sample: C2C12 mouse myoblast cell line
Immunocytochemistry
Sample: Immersion fixed C2C12 mouse myoblast cell line
Reviewed Applications
Read 1 review rated 5 using MAB9727 in the following applications:
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: Fibroblast Activation Protein alpha/FAP
References
- Zi, F. et al. (2015) Mol. Med. Rep. 11:3203.
- Pineiro-Sanchez, M.L. et al. (1997) J. Biol. Chem. 272:7595.
- Niedermeyer, J. et al. (1997) Int. J. Cancer 71:383.
- Scanlan, M.J. et al. (1994) Proc. Natl. Acad. Sci. USA 91:5657.
- Park, J.E. et al. (1999) J. Biol. Chem. 274:36505.
- Rettig, W.J. et al. (1988) Proc. Natl. Acad. Sci. USA 85:3110.
- Bauer, S. et al. (2006) Arthritis Res. 8:R171.
- Aertgeerts, K. et al. (2005) J. Biol. Chem. 280:19441.
- Keane, F.M. et al. (2011) FEBS J. 278:1316.
- Ghersi, G. et al. (2006) Cancer Res. 66:4652.
- Ghersi, G. et al. (2002) J. Biol. Chem. 277:29231.
- Cheng, J.D. et al. (2005) Mol. Cancer Ther. 4:351.
- Cheng, J.D. et al. (2002) Cancer Res. 62:4767.
- Kraman, M. et al. (2010) Science 330:827.
Alternate Names
Gene Symbol
UniProt
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Product Documents for Mouse Fibroblast Activation Protein alpha /FAP Antibody
Certificate of Analysis
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Product Specific Notices for Mouse Fibroblast Activation Protein alpha /FAP Antibody
For research use only
Related Research Areas
Citations for Mouse Fibroblast Activation Protein alpha /FAP Antibody
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Customer Images
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Application: Flow CytometrySample Tested: NIH-3T3 mouse embryonic fibroblast cell lineSpecies: MouseVerified Customer | Posted 08/26/2025Used 3uL for 15mins at 4°C on 3T3 cells transduced to over express murine FAP. Other murine FAP antibodies give minimal shift but this AF647-conjugated antibodies gave a really terrific shift
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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