Latrophilin 3/LPHN3 Antibody - BSA Free
Novus Biologicals | Catalog # NLS1138
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.
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Description
Scientific Data Images for Latrophilin 3/LPHN3 Antibody - BSA Free
Immunohistochemistry-Paraffin: Latrophilin 3/LPHN3 Antibody - BSA Free [NLS1138]
Immunohistochemistry-Paraffin: Latrophilin 3/LPHN3 Antibody [NLS1138] - Analysis of anti-LPHN3 / Latrophilin-3 antibody with human brain, glioblastoma.Immunohistochemistry-Paraffin: Latrophilin 3/LPHN3 Antibody - BSA Free [NLS1138]
Immunohistochemistry-Paraffin: Latrophilin 3/LPHN3 Antibody [NLS1138] - Analysis of anti-LPHN3 / Latrophilin-3 antibody with brain neurons at 2 ug/ml.Western Blot: Latrophilin 3/LPHN3 Antibody - BSA Free [NLS1138] -
Confirmation of possible FLOT1-/FLOT2-positive early endosome cargo proteins.a Co-IP of FLOT1 with possible cargo proteins detected by DIA-LC-MS/MS analysis of FLOT1-/FLOT2-positive early endosomes (n = 1). b Average DIA protein abundance for LPHN1, LPHN2, LPHN3, CLTA, EEA1, and RAB5C. Data are presented as mean values + SD (n = 3, biologically independent samples over three independent experiments). Significance based on Student’s unpaired two-sided t test; range: ∗P < 0.05, ∗∗P < 0.01; exact P values: LPHN1 (0.022), LPHN2 (0.004), LPHN3 (0.044), CLTA (0.047), EEA1 (0.035), RAB5C (0.008). c Co-IP of FLOT1 and FLOT2 with LPHN1, LPHN2, and LPHN3. LDLR serves as marker for plasma membrane and clathrin-mediated endocytosis. d Immunostaining of HeLa cells for FLOT1 and FLOT2 in combination with LPHN1, LPHN2, and LPHN3 (n = 3). Lower panels show a zoom-in for regions indicated in full-size images. Mander’s coefficients were determined to assess signal overlap between individual populations. Data are presented as mean values + SD (n = 3, cells examined over one experiment). Profile plots indicate the degree of colocalization for individual vesicles. Scale bars = 5 uM; Cntrl. control, IN input, WA wash, EL eluate. Source data are provided as a Source Data file. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36266287), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Latrophilin 3/LPHN3 Antibody - BSA Free
Immunohistochemistry-Paraffin
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Background: Latrophilin 3/LPHN3
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Additional Latrophilin 3/LPHN3 Products
Product Documents for Latrophilin 3/LPHN3 Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for Latrophilin 3/LPHN3 Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for Latrophilin 3/LPHN3 Antibody - BSA Free
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Protocols
View specific protocols for Latrophilin 3/LPHN3 Antibody - BSA Free (NLS1138):
Immunohistochemistry
1. Prepare tissue with formalin fixation and by embedding it in paraffin wax.
2. Make 4 um sections and place on pre-cleaned and charged microscope slides.
3. Heat in a tissue-drying oven for 45 minutes @ 60 degrees Celcius.
4. Deparaffinize the tissues by wash drying the slides in 3 changes of xylene for 5 minutes each @ RT.
5. Rehydrate the tissues by washing the slides in 3 changes of 100% alcohol for 3 minutes each @ RT.
6. Wash the slides in 2 changes of 95% alcohol for 3 minutes each @ RT.
7. Wash the slides in 1 change of 80% alcohol for 3 minutes @ RT.
8. Rinse the slides in gentle running distilled water for 5 minutes @ RT.
9. Perform antigen retrieval by steaming the slides in 0.01M sodium citrate buffer (pH 6.0) @ 99-100 degrees Celcius
for 20 minutes.
10. Remove the slides from the heat and let stand in buffer @ RT for 20 minutes.
11. Rinse the slides in 1X TBS-T for 1 minute @ RT.
**Do not allow the tissues to dry at any time during the staining procedure**
12. Begin the immunostaining by applying a universal protein block for 20 minutes @ RT.
13. Drain protein block from the slides and apply the diluted primary antibody for 45 minutes @ RT.
14. Rinse the slide in 1X TBS-T for 1 minute @ RT.
15. Apply a biotinylated anti-rabbit IgG (H+L) secondary for 30 minutes @ RT.
16. Rinse the slide in 1X TBS-T for 1 minute @ RT.
17. Apply an alkaline phosphatase steptavidin for 30 minutes @ RT.
18. Rinse the slide in 1X TBS-T for 1 minute @ RT.
19. Apply an alkaline phosphatase chromagen substrate for 30 minutes @ RT.
20. Rinse the slide in distilled water for 1 minute @ RT.
**This method should only be used if the chromagen substrate is alcohol insoluble (ie: Vector Red, DAB)**
21. Dehydrate the tissue by washing the slides in 2 changes of 80% alcohol for 1 minute each @ RT.
22. Wash the slides in 2 changes of 95% alcohol for 1 minute each @ RT.
23. Wash the slides in 3 changes of 100% alcohol for 1 minute each @ RT.
24. Wash the slides in 3 changes of xylene for 1 minute each @ RT.
25. Apply cover slip.
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
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars