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Key Product Details
Validated by
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Met1-Ala782
Accession # P06396
Specificity
Clonality
Host
Isotype
Scientific Data Images for Gelsolin/GSN Antibody (893205)
Detection of Gelsolin/GSN in Human Renal Cell Carcinoma via seqIF™ staining on COMET™
Gelsolin/GSN was detected in immersion fixed paraffin-embedded sections of human Renal Cell Carcinoma using Mouse Anti-Human Gelsolin/GSN, pan Monoclonal Antibody (Catalog # MAB8170) at 20ug/mL at 37 ° Celsius for 4 minutes. Before incubation with the primary antibody, tissue underwent an all-in-one dewaxing and antigen retrieval preprocessing using PreTreatment Module (PT Module) and Dewax and HIER Buffer H (pH 9; Epredia Catalog # TA-999-DHBH).Tissue was stained using the Alexa Fluor™ 647 Goat anti-Mouse IgG Secondary Antibody at 1:200 at 37 ° Celsius for 2 minutes. (Yellow; Lunaphore Catalog # DR647MS) and counterstained with DAPI (blue; Lunaphore Catalog # DR100). Specific staining was localized to the cytoplasm. Protocol available in COMET™ Panel Builder.Detection of Human, Mouse, and Rat Gelsolin/GSN by Western Blot.
Western blot shows lysates of SK-Mel-28 human malignant melanoma cell line, MEF mouse embryonic feeder cells, and NR8383 rat alveolar macrophage cell line. PVDF membrane was probed with 0.5 µg/mL of Mouse Anti-Human/Mouse/Rat Gelsolin/GSN Monoclonal Antibody (Catalog # MAB8170) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for Gelsolin/GSN at approximately 95 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.Detection of Human Gelsolin/GSN by Simple WesternTM.
Simple Western shows lysates of Exosome Standards (HT‑29) (NBP3-11685), Exosome Standards (U‑87 MG) (NBP2-49844) and SK‑Mel‑28 human malignant melanoma cell line, loaded at 0.5 mg/ml. A specific band was detected for Gelsolin/GSN at approximately 90 kDa (as indicated) using 20 µg/mL of Mouse Anti-Human/Mouse/Rat Gelsolin/GSN Monoclonal Antibody (Catalog # MAB8170). This experiment was conducted under reducing conditions and using the 12-230kDa separation system.Gelsolin/GSN in Human Kidney.
Gelsolin/GSN was detected in formalin fixed paraffin-embedded sections of human kidney using Mouse Anti-Human/Mouse/Rat Gelsolin/GSN Monoclonal Antibody (Catalog # MAB8170) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS002) and counterstained with hematoxylin (blue). Specific staining was localized to glomeruli and distal convoluted tubules. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Western Blot Shows Human Gelsolin/GSN Specificity Using Knockout Cell Line.
Western blot shows lysates of U2OS human osteosarcoma cell line and Gelsolin/GSN knockout U2OS cell line (KO). Nitrocellulose membrane was probed with 0.1 µg/mL of Mouse Anti-Human/Mouse/Rat Gelsolin/GSN Monoclonal Antibody (Catalog # MAB8170) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody. A specific band was detected for Gelsolin/GSN at approximately 80 kDa (as indicated) in the parental U2OS cell line, but is not detectable in knockout U2OS cell line. The Ponceau stained transfer of the blot is shown. This experiment was conducted under reducing conditions. Image, protocol, and testing courtesy of YCharOS Inc. See ycharos.com for additional details.Detection of hbahwou3etm9tvbh4pxm.jpg by Immunohistochemistry
GSN expression in muscle pericytes and fibroblasts. (A) Immunohistochemical analysis of GSN and CD13 (pericyte marker) expression in mouse TA muscle. (B) Quantification revealed GSN expression in approximately 90% of CD13+ pericytes in TA muscle. n = 4 mice. Data were shown as mean ± SD. (C) Immunohistochemical analysis of GSN and vimentin (fibroblast marker) expression in mouse TA muscle. (D) Quantification revealed GSN expression in approximately 14% of vimentin+ fibroblasts in TA muscle. n = 4 mice. Data were shown as mean ± SD. Image collected and cropped by CiteAb from the following open publication (https://www.nature.com/articles/s41598-025-14225-3), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Gelsolin/GSN by Immunohistochemistry
GSN expression in muscle pericytes and fibroblasts. (A) Immunohistochemical analysis of GSN and CD13 (pericyte marker) expression in mouse TA muscle. (B) Quantification revealed GSN expression in approximately 90% of CD13+ pericytes in TA muscle. n = 4 mice. Data were shown as mean ± SD. (C) Immunohistochemical analysis of GSN and vimentin (fibroblast marker) expression in mouse TA muscle. (D) Quantification revealed GSN expression in approximately 14% of vimentin+ fibroblasts in TA muscle. n = 4 mice. Data were shown as mean ± SD. Image collected and cropped by CiteAb from the following open publication (https://www.nature.com/articles/s41598-025-14225-3), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Gelsolin/GSN Antibody (893205)
COMET
Immunohistochemistry
Sample: Formalin fixed paraffin-embedded sections of human kidney
Knockout Validated
Multiplex Immunofluorescence
Sample: Immersion fixed paraffin-embedded sections of human Renal Cell Carcinoma
Simple Western
Sample: Exosome Standards (HT-29) (Catalog # NBP3-11685), Exosome Standards (U-87 MG) (Catalog # NBP2-49844) and SK‑Mel‑28 human malignant melanoma cell line
Western Blot
Sample: SK‑Mel‑28 human malignant melanoma cell line, MEF mouse embryonic feeder cells, and NR8383 rat alveolar macrophage cell line
Reviewed Applications
Read 1 review rated 5 using MAB8170 in the following 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: Gelsolin/GSN
Alternate Names
Gene Symbol
UniProt
Additional Gelsolin/GSN Products
Product Documents for Gelsolin/GSN Antibody (893205)
Certificate of Analysis
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Product Specific Notices for Gelsolin/GSN Antibody (893205)
For research use only
Related Research Areas
Citations for Gelsolin/GSN Antibody (893205)
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Application: ImmunohistochemistrySample Tested: Pancreas tissueSpecies: MouseVerified Customer | Posted 02/09/2022
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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