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
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Val162-Gly253
Accession # Q8BJ56
Specificity
Clonality
Host
Isotype
Scientific Data Images for PEDFR/PNPLA2 Antibody
Detection of Human and Mouse PEDF R/PNPLA2 by Western Blot.
Western blot shows lysates of human adipose tissue and mouse adipose tissue. PVDF membrane was probed with 1 µg/mL of Sheep Anti-Human/Mouse/Rat PEDF R/PNPLA2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5365) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for PEDF R/PNPLA2 at approximately 55 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.PEDF R/PNPLA2 in Mouse Kidney.
PEDF R/PNPLA2 was detected in perfusion fixed frozen sections of mouse kidney using 15 µg/mL Sheep Anti-Human/Mouse/Rat PEDF R/PNPLA2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5365) 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 the plasma membrane of epithelial cells in tubules. View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections.Detection of Mouse PEDF R/PNPLA2 by Simple WesternTM.
Simple Western lane view shows lysates of mouse adipose tissue, loaded at 0.2 mg/mL. A specific band was detected for PEDF R/PNPLA2 at approximately 59 kDa (as indicated) using 10 µg/mL of Sheep Anti-Human/Mouse/Rat PEDF R/PNPLA2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5365) followed by 1:50 dilution of HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.Detection of Human PEDFR/PNPLA2/ATGL by Western Blot
Loss-of-function analyses of PEDF in Bkid cells. (A) PEDF micro RNA (miR) expressing vector was transfected into Bkid cells. Immunoblot by anti-PEDF antibody showed the reduction of PEDF proteins by miRs. (B) The renal and the hepatic lesions of the results of the intracardiac injections of Bkid cells or Bkid+PEDFmiR cells. The adrenal metastasis was observed. Also, by Bkid cell injections, the renal metastasis was observed frequently (left, 12-positive/12), while no renal nodule was observed in Bkid+PEDFmiR injected mouse (right, 17-negative/18). The ruler is 1mm square. (C) The hepatic metastases of both cells were not inhibited with or without PEDF. (D) The section Hematoxylin/Eosin (H&E) staining of the similar samples to (B). The adrenal hypertrophy was observed both in Bkid- and Bkid+PEDFmiR-injected mouse organs. The renal metastatic lesion (met) was seen as the lighter color. The scale is 2 mm. (E) The hepatic metastasis. Both tumors had the cavity. (F) PEDF-immunohistochemistry (IHC) of the section (D). PEDF staining was observed inside of the adrenal gland cystic vesicle of Bkid tumors. The overall staining level of PEDF in Bkid tumor was higher than Bkid+PEDFmiR cells. The scale is 1 mm. (G) IHC for PEDF on paraffin sections of collagen gel-embedded 143B and 143B+PEDF cells. (H-L) The renal section IHC by various antibodies. (H) Anti-SPARC (osteonectin)-IHC indicates that the lesions are derived from the injected osteosarcoma. In the section of kidney from Bkid-injected mouse, there is SPARC-positive tumor both in kidney and adrenal gland sides. On the right, the kidney from Bkid+PEDFmiR-injected mouse had SPARC-positive cells only in adrenal gland. The scale indicates 100 µm. (I–L) The scale indicates 20 µm. (I) The higher magnified picture of the tissue surrounded glomerulus. There is SPARC-positive cells were seen around the glomerulus of Bkid-injected mouse (arrow), while no signal was seen in Bkid+PEDFmiR-injected mouse, (J) PEDF-IHC. PEDF was accumuDetection of PEDFR/PNPLA2 by Western Blot
Effect of the 29-mer on the expression of MMP-9 in EDE. The schedule of induction of EDE is described in Fig. 2. (A) Representative immunofluorescence images showing MMP-9 in corneal and conjunctival epithelia after 14 days of EDE induction (n = 6 per group). (B) qPCR evaluates the levels of MMP-9 in the ocular surface epithelia (n = 6 per group). (C and D) Representative Western blots and densitometric analyses of MMP-9 and PEDF-R of ocular surface epithelia are shown from three independent experiments. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36201200), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of PEDFR/PNPLA2 by Western Blot
Effect of the 29-mer on the expression of MMP-9 in EDE. The schedule of induction of EDE is described in Fig. 2. (A) Representative immunofluorescence images showing MMP-9 in corneal and conjunctival epithelia after 14 days of EDE induction (n = 6 per group). (B) qPCR evaluates the levels of MMP-9 in the ocular surface epithelia (n = 6 per group). (C and D) Representative Western blots and densitometric analyses of MMP-9 and PEDF-R of ocular surface epithelia are shown from three independent experiments. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36201200), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for PEDFR/PNPLA2 Antibody
Immunohistochemistry
Sample: Perfusion fixed frozen sections of mouse kidney
Simple Western
Sample: Mouse adipose tissue
Western Blot
Sample: Human adipose tissue and mouse adipose tissue
Reviewed Applications
Read 1 review rated 3 using AF5365 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: PEDFR/PNPLA2
Long Name
Alternate Names
Gene Symbol
UniProt
Additional PEDFR/PNPLA2 Products
Product Documents for PEDFR/PNPLA2 Antibody
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 PEDFR/PNPLA2 Antibody
For research use only
Related Research Areas
Citations for PEDFR/PNPLA2 Antibody
Customer Reviews for PEDFR/PNPLA2 Antibody (1)
Have you used PEDFR/PNPLA2 Antibody?
Submit a review and receive an Amazon gift card!
$25/€18/£15/$25CAN/¥2500 for a review with an image
$10/€7/£6/$10CAN/¥1110 for a review without an image
Submit a review
Customer Images
-
Application: Immunocytochemistry/ImmunofluorescenceSample Tested: Skin tissueSpecies: MouseVerified Customer | Posted 01/17/2018
There are no reviews that match your criteria.
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