Mouse Intelectin‑1/Omentin Antibody
R&D Systems | Catalog # MAB8074
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Ala20-Ser298
Accession # O88310
Specificity
Clonality
Host
Isotype
Scientific Data Images for Mouse Intelectin‑1/Omentin Antibody
Detection of Mouse Intelectin‑1/Omentin by Western Blot.
Western blot shows lysates of mouse small intestine tissue. PVDF membrane was probed with 2 µg/mL of Rat Anti-Mouse Intelectin-1/Omentin Monoclonal Antibody (Catalog # MAB8074) followed by HRP-conjugated Anti-Rat IgG Secondary Antibody (Catalog # HAF005). A specific band was detected for Intelectin-1/Omentin at approximately 35 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Intelectin‑1/Omentin in Mouse Intestine.
Intelectin-1/Omentin was detected in perfusion fixed frozen sections of mouse intestine using Rat Anti-Mouse Intelectin-1/Omentin Monoclonal Antibody (Catalog # MAB8074) at 25 µg/mL overnight at 4 °C. Tissue was stained using the NorthernLights™ 557-conjugated Anti-Rat IgG Secondary Antibody (red; Catalog # NL013) and counterstained with DAPI (blue). Specific staining was localized to Paneth cells in intestinal glands. View our protocol for Fluorescent IHC Staining of Frozen Tissue Sections.
Detection of Intelectin-1/Omentin by Immunohistochemistry
Microbiota suppresses transcriptional nutrient stress response and activates mTOR signaling. A) Overlay of nutrient starvation stress response transcription factor genes upon gene expression volcano plot of all GF and SPF epithelial cells. B) Violin plot of Atf3 and Jun expression across GF and SPF epithelial cells. C) Violin plot of Fos expression across GF and SPF epithelial cells and quantification and representative image of Fos in situ hybridization within GF and SPF jejunal/ileal small intestinal crypts. D) Violin plots and E) UMAP visualization of Rps6kb1 and Rps6 epithelial subsets in GF and SPF epithelial cells. *, p < .01 comparing GF and SPF clusters by Wilcoxon rank sum test and >0.75 Log2 fold change. F) pS6 staining and quantification of jejunal/ileal small intestinal crypts from GF and SPF mice. G) Immunofluorescence co-staining of BrdU, pS6, and Itln1 in GF and SPF jejunal/ileal small intestinal crypts. Arrows indicate co-expression of Itln1 and pS6. Representative images shown (n = 4–6). Each point represents the mean quantification 20 crypts from one mouse (n = 4–6). Stains were quantified using CellProfiler. Bars represent mean ± SEM. **, p < .005 by two-tailed Student’s t-test. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35939622), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Intelectin-1/Omentin by Immunohistochemistry
Microbiota suppresses transcriptional nutrient stress response and activates mTOR signaling. A) Overlay of nutrient starvation stress response transcription factor genes upon gene expression volcano plot of all GF and SPF epithelial cells. B) Violin plot of Atf3 and Jun expression across GF and SPF epithelial cells. C) Violin plot of Fos expression across GF and SPF epithelial cells and quantification and representative image of Fos in situ hybridization within GF and SPF jejunal/ileal small intestinal crypts. D) Violin plots and E) UMAP visualization of Rps6kb1 and Rps6 epithelial subsets in GF and SPF epithelial cells. *, p < .01 comparing GF and SPF clusters by Wilcoxon rank sum test and >0.75 Log2 fold change. F) pS6 staining and quantification of jejunal/ileal small intestinal crypts from GF and SPF mice. G) Immunofluorescence co-staining of BrdU, pS6, and Itln1 in GF and SPF jejunal/ileal small intestinal crypts. Arrows indicate co-expression of Itln1 and pS6. Representative images shown (n = 4–6). Each point represents the mean quantification 20 crypts from one mouse (n = 4–6). Stains were quantified using CellProfiler. Bars represent mean ± SEM. **, p < .005 by two-tailed Student’s t-test. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35939622), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse Intelectin‑1/Omentin Antibody
Immunohistochemistry
Sample: Perfusion fixed frozen sections of mouse intestine
Western Blot
Sample: Mouse small intestine tissue
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: Intelectin-1/Omentin
Alternate Names
Gene Symbol
UniProt
Additional Intelectin-1/Omentin Products
Product Documents for Mouse Intelectin‑1/Omentin Antibody
Product Specific Notices for Mouse Intelectin‑1/Omentin Antibody
For research use only
Citations for Mouse Intelectin‑1/Omentin 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
- 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