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Key Product Details
Species Reactivity
Validated:
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Applications
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Cited:
Label
Antibody Source
Product Specifications
Immunogen
Cys2-Ala132
Accession # P15090
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human FABP4/A-FABP Antibody
Detection of Human, Mouse, and Rat FABP4/A‑FABP by Western Blot.
Western blot shows lysates of human heart tissue, rat heart tissue, mouse heart tissue, human adipose tissue, rat adipose tissue, and mouse adipose tissue. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human FABP4/A-FABP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3150) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF019). A specific band was detected for FABP4/A-FABP at approximately 14 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.FABP4/A‑FABP in Human Bladder Cancer Tissue.
FABP4/A-FABP was detected in immersion fixed paraffin-embedded sections of human bladder cancer tissue using Goat Anti-Human FABP4/A-FABP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3150) at 3 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Detection of Human and Mouse FABP4/A‑FABP by Simple WesternTM.
Simple Western lane view shows lysates of human heart tissue and mouse heart tissue, loaded at 0.2 mg/mL. A specific band was detected for FABP4/A-FABP at approximately 19 kDa (as indicated) using 10 µg/mL of Goat Anti-Human FABP4/A-FABP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3150) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.Human/Mouse FABP4/A‑FABP ELISA Standard Curve.
Recombinant Human/Mouse FABP4/A‑FABP protein was serially diluted 2-fold and captured by Rat Anti-Human/Mouse FABP4/A‑FABP Monoclonal Antibody (MAB3150) coated on a Clear Polystyrene Microplate (DY990). Goat Anti-Human FABP4/A‑FABP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3150) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (DY998) followed by Substrate Solution (DY999) and stopping the enzymatic reaction with Stop Solution (DY994).Detection of FABP4 by Immunohistochemistry
Expression profiles of FABP4 and FABP5 in normal breast tissue. A–D Representative hematoxylin and eosin (H&E) staining of normal breast tissue, showing lobules (A), ducts (B), adipocytes (C), and blood vessels (D). Scale bar: 100 μm. E–H Representative immunostaining for FABP4 (red) in normal breast tissue, including lobules (E), ducts (F), adipocytes (G), and blood vessels (H). Scale bar: 100 μm. I, J Analysis of colocalization of vWF (brown) (I) and FABP4 (red) (J) expression in normal breast tissue. Scale bar: 100 μm. K, L Analysis of colocalization of CD163 (brown) (K) and FABP4 (red) (L) expression in normal breast tissue. Scale bar: 100 μm. M–O Representative immunostaining for FABP5 (red) and vWF (brown) in normal breast tissue, showing adipocytes (M), blood vessels (N), and epithelium (O). Scale bar: 100 μm. P Comparison of FABP4 and FABP5 expression levels across different cell types in normal breast tissue, including epithelium, myoepithelium, adipocytes, endothelium, and macrophages (n = 9 for each group). The scoring on a 1-to-5 scale was performed for all cells. Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s12672-025-02117-x), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of FABP4 by Immunohistochemistry
FABP4 expression pattern in breast cancer tissue. A–D Representative H&E staining of ductal carcinoma in situ (DCIS), including DCIS regions (A), surrounding immune cells (B), adipocytes (C), and stromal vessel (D). Scale bars: 100 μm. E–J Representative immunostaining for FABP4 (red), CD163 (brown) and VWF (brown) in DCIS breast tissue, including DCIS regions (E), immune cells (F), adipocytes (G), and stromal vessels (H). Scale bars: 100 μm. I–M Representative immunostaining for FABP4 in invasive frontline tumor cells and adjacent adipose tissue. Most tumor cells were negative for FABP4 (J). Tumor cells close to adipocytes were positive for FABP4 (black arrow) (K). Adipocytes adjacent to tumor cells were small (L). Adipocytes away from tumor were large (M). Scale bar for I: 200 μm, scale bar for panel J-M: 100 μm, (N) Comparison of adipocyte sizes at varying distances from tumor cells (p < 0.0001, n = 40 cells). Image collected and cropped by CiteAb from the following open publication (https://link.springer.com/10.1007/s12672-025-02117-x), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human FABP4/A-FABP Antibody
ELISA
This antibody functions as an ELISA detection antibody when paired with Rat Anti-Human/Mouse FABP4/A‑FABP Monoclonal Antibody (Catalog # MAB3150).
This product is intended for assay development on various assay platforms requiring antibody pairs. We recommend the Human FABP4/A-FABP DuoSet ELISA Kit (Catalog # DY3150-05) for convenient development of a sandwich ELISA or the Human FABP4 Quantikine ELISA Kit (Catalog # DFBP40) for a complete optimized ELISA.
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human normal adipose, normal heart, and bladder cancer tissue
Simple Western
Sample: Human heart tissue and mouse heart tissue
Western Blot
Sample: Human heart tissue, rat heart tissue, mouse heart tissue, human adipose tissue, rat adipose tissue, and mouse adipose tissue
Reviewed Applications
Read 1 review rated 4 using AF3150 in the following applications:
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: FABP4/A-FABP
Long Name
Alternate Names
Gene Symbol
UniProt
Additional FABP4/A-FABP Products
Product Documents for Human FABP4/A-FABP Antibody
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Human FABP4/A-FABP Antibody
For research use only
Related Research Areas
Citations for Human FABP4/A-FABP Antibody
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Application: ImmunofluorescenceSample Tested: See PMID 23423575Species: HumanVerified Customer | Posted 01/07/2015
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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
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- 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
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- 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
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- 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