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Key Product Details
Species Reactivity
Mouse
Applications
Immunohistochemistry, Western Blot, COMET
Label
Unconjugated
Antibody Source
Monoclonal Rat IgG2A Clone # 1123826
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Product Specifications
Immunogen
Chinese Hamster Ovary cell line, CHO-derived mouse EMR-1
Met1-Ser590
Accession # Q61549
Met1-Ser590
Accession # Q61549
Specificity
Detects recombinant mouse F4/80 protein in Direct ELISA.
Clonality
Monoclonal
Host
Rat
Isotype
IgG2A
Scientific Data Images for Mouse F4/80 Antibody (1123826)
Detection of EMR1 in Mouse Spleen via seqIF™ staining on COMET™
EMR-1 was detected in immersion fixed paraffin-embedded sections of mouse spleen using Rat Anti-Mouse EMR-1 Monoclonal Antibody (Catalog # MAB11811) at 3ug/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-Rat IgG Secondary Antibody at 1:200 at 37 ° Celsius for 2 minutes. (Yellow; Lunaphore Catalog # DR647RT) and counterstained with DAPI (blue; Lunaphore Catalog # DR100). Specific staining was localized to the membrane. Protocol available in COMET™ Panel Builder.Detection of EMR1 in Mouse Testis via seqIF™staining on COMET™
EMR-1 was detected in immersion fixed paraffin-embedded sections of mouse testis using Rat Anti-Mouse EMR-1 Monoclonal Antibody (Catalog # MAB11811) at 3ug/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-Rat IgG Secondary Antibody at 1:200 at 37 ° Celsius for 2 minutes. (Yellow; Lunaphore Catalog # DR647RT) and counterstained with DAPI (blue; Lunaphore Catalog # DR100). Specific staining was localized to the membrane. Protocol available in COMET™ Panel Builder.Detection of EMR1 in Mouse Liver via seqIF™staining on COMET™
EMR-1 was detected in immersion fixed paraffin-embedded sections of mouse liver using Rat Anti-Mouse EMR-1 Monoclonal Antibody (Catalog # MAB11811) at 3ug/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-Rat IgG Secondary Antibody at 1:200 at 37 ° Celsius for 2 minutes. (Yellow; Lunaphore Catalog # DR647RT) and counterstained with DAPI (blue; Lunaphore Catalog # DR100). Specific staining was localized to the membrane. Protocol available in COMET™ Panel Builder.Detection of EMR1 in Mouse Kidney viaseqIF™ staining on COMET™
EMR-1 was detected in immersion fixed paraffin-embedded sections of mouse kidney using Rat Anti-Mouse EMR-1 Monoclonal Antibody (Catalog # MAB11811) at 3ug/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-Rat IgG Secondary Antibody at 1:200 at 37 ° Celsius for 2 minutes. (Yellow; Lunaphore Catalog # DR647RT) and counterstained with DAPI (blue; Lunaphore Catalog # DR100). Specific staining was localized to the membrane. Protocol available in COMET™ Panel Builder.Detection of Mouse F4/80 by Western Blot.
Western Blot shows lysates of mouse spleen and J774A.1 mouse reticulum cell sarcoma macrophage cell line. PVDF membrane was probed with 2 µg/ml of Rat Anti-Mouse F4/80 Monoclonal Antibody (Catalog # MAB11811) followed by HRP-conjugated Anti-Rat IgG Secondary Antibody (HAF005). A specific band was detected for F4/80 at approximately 130-300 kDa (as indicated). This experiment was conducted under reducing conditions and using Western Blot Buffer Group 1.Perfusion fixed paraffin-embedded sections of mouse liver
F4/80 was detected in perfusion fixed paraffin-embedded sections of mouse liver using Rat Anti-Mouse F4/80 Monoclonal Antibody (Catalog # MAB11811) at 5 µg/ml overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using VisUCyte Antigen Retrieval Reagent-Basic (VCTS021). Tissue was stained using the HRP-conjugated Anti-Rat IgG Secondary Antibody (HAF005) and counterstained with hematoxylin (blue). Specific staining was localized to the membrane. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Perfusion fixed paraffin-embedded sections of mouse spleen
F4/80 was detected in perfusion fixed paraffin-embedded sections of mouse spleen using Rat Anti-Mouse F4/80 Monoclonal Antibody (Catalog # MAB11811) at 5 µg/ml overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using VisUCyte Antigen Retrieval Reagent-Basic (VCTS021). Tissue was stained using the HRP-conjugated Anti-Rat IgG Secondary Antibody and counterstained with hematoxylin (blue). Specific staining was localized to the membrane. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Applications for Mouse F4/80 Antibody (1123826)
Application
Recommended Usage
COMET
3 µg/mL
Sample: Immersion fixed paraffin-embedded sections of mouse spleen, mouse testis, mouse liver and mouse kidney.
Sample: Immersion fixed paraffin-embedded sections of mouse spleen, mouse testis, mouse liver and mouse kidney.
Immunohistochemistry
0.25-25 µg/mL
Sample: Perfusion fixed paraffin-embedded sections of mouse spleen and sections of mouse liver
Sample: Perfusion fixed paraffin-embedded sections of mouse spleen and sections of mouse liver
Western Blot
2 µg/mL
Sample: Mouse spleen and J774A.1 mouse reticulum cell sarcoma macrophage cell line
Sample: Mouse spleen and J774A.1 mouse reticulum cell sarcoma macrophage cell line
Formulation, Preparation, and Storage
Purification
Protein A or G purified from hybridoma culture supernatant
Reconstitution
Reconstitute lyophilized material at 0.2 mg/ml in sterile PBS. For liquid material, refer to CoA for concentration.
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Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose.
Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 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: F4/80
Alternate Names
DD7A5-7, Gpf480, Ly71
Gene Symbol
ADGRE1
UniProt
Additional F4/80 Products
Product Documents for Mouse F4/80 Antibody (1123826)
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Mouse F4/80 Antibody (1123826)
For research use only
Related Research Areas
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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
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