Progranulin, also known as acrogranin, PC cell-derived growth factor (PCDGF) and epithelin/granulin precursor, is a ubiquitously expressed, 88 kDa, secreted glycoprotein (1‑3). Structurally, it belongs to none of the well-established growth factor families (4). Mouse Progranulin is 589 amino acids (aa) in length and contains a 17 aa signal sequence and a 572 aa mature region that has four potential sites for N-linked glycosylation. It has a highly repetitive organization, containing seven tandem copies of a 55‑57 aa consensus motif that contains 12 conserved cysteine residues: VXCX5-6CX5CCX8CCX6CCXDX2HCCPX4CX5-6CX2 (1). Progranulin is secreted in an intact form (2, 4) or undergoes proteolysis leading to the release of multiple peptides made from the seven tandem repeats, the granulins (5‑7). Mouse Progranulin shares 87% and 75% aa sequence identity with rat and human Progranulin, respectively. Progranulin is involved in the regulation of cellular proliferation, as well as differentiation, development, and pathological processes (4). It has been isolated as a differentially expressed gene during mesothelial differentiation (8), macrophage development (9), development synovium of rheumatoid arthritis and osteoarthritis (10), sexual differentiation of the brain (11), and has also been shown to be a mediator of cartilage proliferation plus of wound response and tissue repair (4, 12‑13). High levels of Progranulin expression have been found to be associated with several human cancers, and are believed to contribute to tumorigenesis in breast cancer, clear cell renal carcinoma, invasive ovarian carcinoma, glioblastoma, adipocyte teratoma, and multiple myeloma (4, 5, 12, 14‑20).
Mouse Progranulin/PGRN Antibody (333731)
R&D Systems | Catalog # MAB25571
Scientific images may be resized, cropped, or adjusted for brightness or contrast for presentation purposes. These updates are limited to presentation and do not affect the underlying scientific interpretation of the data. Where available, additional source data may be provided upon request.
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Thr18-Leu589
Accession # P28798
Specificity
Clonality
Host
Isotype
Scientific Data Images for Mouse Progranulin/PGRN Antibody (333731)
Progranulin in Mouse Kidney.
Progranulin was detected in perfusion fixed frozen sections of mouse kidney using Rat Anti-Mouse Progranulin Monoclonal Antibody (Catalog # MAB25571) at 25 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Rat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS017) and counterstained with hematoxylin (blue). View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections.Detection of Progranulin by Flow Cytometry
PGRN promoted immunosuppressive M2-like TAMs accumulate and induces CD8+T cells exclusion. A, B Percentage of M1 macrophages (F4/80+CD86+), M2 macrophages (F4/80+CD206+) overtime were assessed by flow cytometry analysis (A), quantification of M1 and M2 macrophages (B). C Immunofluorescent images of M1-like TAM markers and M2-like TAM markers; scale bar, 100um and 50um respectively. D–F TAMs isolated from breast cancer tissues were tested for their ability to suppress CD28/CD3 stimulated splenic CD8+T cell proliferation (CFSE dilution and Ki67.+ cells; D, E) and activation (IFN gamma level; F) Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s00262-024-03655-z), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Progranulin by Flow Cytometry
PGRN promoted tumor growth by inducing CD8+T cell exclusion in BCa tissue. A IHC images of PGRN level in human breast cancer and paracancerous tissue sections (n = 68); scale bar, 50um. B Quantification of PGRN level in human breast cancer and paracancerous tissue sections (n = 68). C Breast cancer PY8119 cells were injected in situ into the fat pads of C57 wild-type mice and PGRN knock-out mice (n = 6 per group) and tumor volume curve; scale bar,10mm. D Percentage of CD8+ T cells over time assessed by flow cytometry analysis. E Representative images of MxIHC staining in tumors from WT and PGRN−/−mice; scale bar, 100um. F Percentage of CD69+CD8+T cells and PD-1+CD8+T cells over time assessed by flow cytometry analysis Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s00262-024-03655-z), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Progranulin by Flow Cytometry
PGRN promoted CD8+T cells exclusion by up-regulating ICAM-1 of TAMs. A Mouse-specific chemokine protein array was performed with wild-type (WT) PMs CM and PGRN−/− PMs CM. B Western blot was performed to analyze ICAM-1 expression and quantification. C Percentage of ICAM-1+ macrophages isolated from WT and PGRN−/− BCa tissues was analyzed by flow cytometry and quantification. D–F TAMs isolated from WT tumor were tested for their ability to suppress CD28/CD3 stimulated splenic CD8+T cell proliferation (Ki67+ cells; D), activation (IFN gamma ; E and CD69 levels; F) with the presence or absence of ICAM-1 neutralizing antibody Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s00262-024-03655-z), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Progranulin by Flow Cytometry
PGRN promoted tumor growth by inducing CD8+T cell exclusion in BCa tissue. A IHC images of PGRN level in human breast cancer and paracancerous tissue sections (n = 68); scale bar, 50um. B Quantification of PGRN level in human breast cancer and paracancerous tissue sections (n = 68). C Breast cancer PY8119 cells were injected in situ into the fat pads of C57 wild-type mice and PGRN knock-out mice (n = 6 per group) and tumor volume curve; scale bar,10mm. D Percentage of CD8+ T cells over time assessed by flow cytometry analysis. E Representative images of MxIHC staining in tumors from WT and PGRN−/−mice; scale bar, 100um. F Percentage of CD69+CD8+T cells and PD-1+CD8+T cells over time assessed by flow cytometry analysis Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s00262-024-03655-z), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse Progranulin/PGRN Antibody (333731)
Immunohistochemistry
Sample: Perfusion fixed frozen sections of mouse testis and kidney
Western Blot
Sample: Recombinant Mouse Progranulin (Catalog # 2557-PG) under non-reducing conditions only. We recommend (Catalog # AF2557) for Western blot applications.
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: Progranulin/PGRN
References
- Plowman, G.D. et al. (1992) J. Biol. Chem. 267:13073.
- Zhou, J. et al. (1993) J. Biol. Chem. 268:10863.
- Liu, Y. et al. (2007) BMC Cancer 7:22.
- Xu, K. et al. (2007) J. Biol. Chem. 282:11347.
- Davidson, B. et al. (2004) Cancer 100:2139.
- Zanocco-Marani, T. et al. (1999) Cancer Res. 59:5331.
- Lu, R. and G. Serrero (2000) Proc. Natl. Acad. Sci. U.S.A. 97:3993.
- Sun, X. et al. (2004) Am. J. Respir. Cell Mol. Biol. 30:510.
- Barreda, D.R. et al. (2004) Dev. Comp. Immunol. 28:727
- Justen, H.P. et al. (2000) Mol. Cell Biol. Res. Commun. 3:165.
- Suzuki, M. and M. Nishiahara (2002) Mol. Genet. Metab. 75:31.
- He, Z. et al. (2003) Nat. Med. 9:225.
- Zhu, J. et al. (2002) Cell 111:867.
- He, Z. and A. Bateman (2003) J. Mol. Med. 81:600.
- Bateman, A. et al. (1990) Biochem. Biophys. Res. Commun. 173:1161.
- Gonzalez, E.M. et al. (2003) J. Biol. Chem. 278:38113.
- Jones, M.B. et al. (2003) Gynecol. Oncol. 88:S136.
- Wang, W. et al. (2003) Clin. Cancer Res. 9:2221.
- Zhang, H. and G. Serrero (1998) Proc. Natl. Acad. Sci. U.S.A. 95:14202.
Alternate Names
Gene Symbol
UniProt
Additional Progranulin/PGRN Products
Product Documents for Mouse Progranulin/PGRN Antibody (333731)
Certificate of Analysis
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Product Specific Notices for Mouse Progranulin/PGRN Antibody (333731)
For research use only
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Citations for Mouse Progranulin/PGRN Antibody (333731)
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars