Mouse WISP-1 (Wnt-induced secreted protein-1; also named CNN4) is a 40 kDa, secreted, heparin-binding glycoprotein that is a member of the CCN (or CTGF/Cyr61/Nov) cysteine-rich protein family (1‑6). It is synthesized as a 367 amino acid (aa) precursor that contains a series of structural homology modules. Following a 22 aa signal sequence, there is a 68 aa IGFBP-like domain (aa 53‑120), a 66 aa von Willebrand factor type C (VWC) module (aa 121‑186), a 41 aa TSP type I domain (aa 220‑260) and a 75 aa, C-terminal cysteine knot motif (aa 273‑347) (1, 6). The VWC module is associated with protein-protein interaction, the TSP domain binds sulfated glycoconjugates, and the cysteine knot mediates dimerization and receptor binding (4). It is likely that WISP-1 normally circulates as an 80 kDa homodimer (2). Multiple splice forms are reported for human WISP-1, but none for rodent (7‑9). Mature mouse WISP-1 is 98%, 84% and 85% aa identical to rat, canine and human WISP-1, respectively. WISP-1 is expressed by fibroblasts and osteoblasts, and may contribute to fracture healing by promoting bone cell formation (1, 10, 11).
Mouse WISP-1/CCN4 Antibody
R&D Systems | Catalog # AF1680
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
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Cited:
Label
Antibody Source
Product Specifications
Immunogen
Thr23-Asn367
Accession # O54775
Specificity
Clonality
Host
Isotype
Scientific Data Images for Mouse WISP-1/CCN4 Antibody
WISP‑1/CCN4 in Mouse Embryo.
WISP-1/CCN4 was detected in immersion fixed frozen sections of mouse embryo (13 d.p.c.) using 15 µg/mL Sheep Anti-Mouse WISP-1/CCN4 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1680) overnight at 4 °C. Tissue was stained with the Anti-Sheep HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS019) and counterstained with hematoxylin (blue). Specific labeling was localized to developing epithelial cells in duodenum. View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections.Detection of WISP-1/CCN4 by Immunohistochemistry
CCN4 deletion reduced AAA formation. Aneurysm grade score—representative images of aortic sections stained with EVG and identified as grade 0–4. ApoE−/−CCN4−/− and ApoE−/−CCN4+/+ mice were exposed to AngII for 28 days and aortic sections stained with EVG (a). The mean aneurysm grade score was calculated from the aortic segment exhibiting the highest degree of aneurysm (most dilated/diseased section per aorta graded) (b). The presence (grey/black bars) and absence (white bars) of vessel wall remodelling on the aorta (presence of fibrous adventitial thickening, as seen in grade 3 example, in any of the sections along the aorta) was noted (c). The number of elastin breaks was quantified from the average of 4 thoracic or 4 abdominal aortic segments (d). Representative images of EVG stained aortae to illustrate vessel wall remodelling (e) and elastin breaks (f), indicated by arrowheads at both low and high power. g Physical parameters of the average thoracic and abdominal aortic sections. CCN4+/+ApoE−/− n = 13 and CCN4−/−ApoE−/− n = 12, * indicates p < 0.05 compared to CCN4 + / + controls. Mann–Whitney test for aneurysm score, elastin breaks and physical parameters, data is presented as mean ± sem (B and D); Fisher’s Exact test for adventitial thickening (C) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/34080128), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse WISP-1/CCN4 Antibody
Immunohistochemistry
Sample: Immersion fixed frozen sections of mouse embryo (13 d.p.c.)
Western Blot
Sample: Recombinant Mouse WISP‑1/CCN4 (Catalog # 1680-WS)
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 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: WISP-1/CCN4
References
- Pennica, D. et al. (1998) Proc. Natl. Acad. Sci. USA 95:14717.
- Tanada, S. et al. (2001) Oncogene 20:5525.
- Brigstock, D.R. et al. (2003) J. Clin. Pathol. Mol. Pathol. 56:127.
- Desnoyers, L. (2004) Curr. Pharm. Des. 10:3913.
- Brigstock, D.R. (2003) J. Endocrinol. 178:169.
- Hashimoto, Y. et al. (1998) J. Exp. Med. 187:289.
- SwissProt Accession # O54775.
- SwissProt Accession # Q99PP0.
- SwissProt Accession # O95388
- French, D.M. et al. (2004) Am. J. Pathol. 165:855.
- Parisi, M.S. et al. (2006) Bone 38:671.
Long Name
Alternate Names
Gene Symbol
UniProt
Additional WISP-1/CCN4 Products
Product Documents for Mouse WISP-1/CCN4 Antibody
Certificate of Analysis
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Product Specific Notices for Mouse WISP-1/CCN4 Antibody
For research use only
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Citations for Mouse WISP-1/CCN4 Antibody
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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