Endothelial Lipase Antibody - BSA Free
Novus Biologicals | Catalog # NB400-111
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Scientific Data Images for Endothelial Lipase Antibody - BSA Free
Western Blot: Endothelial Lipase Antibody [NB400-111]
Western Blot: Endothelial Lipase Antibody [NB400-111] - Human endothelial lipase detected in transfected 293 lysates (MW 57 kDa)Immunocytochemistry/ Immunofluorescence: Endothelial Lipase Antibody [NB400-111]
Immunocytochemistry/Immunofluorescence: Endothelial Lipase Antibody [NB400-111] - Antibody was tested in HeLa cells with Dylight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and Dylight 550 (red).Western Blot: Endothelial Lipase Antibody [NB400-111]
Western Blot: Endothelial Lipase Antibody [NB400-111] - Cells were transfected with the pCMV6-ENTRY control or pCMV6-ENTRY LIPG cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-LIPG.Applications for Endothelial Lipase Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry-Frozen
Western Blot
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Background: Endothelial Lipase
Alternate Names
Gene Symbol
Additional Endothelial Lipase Products
Product Documents for Endothelial Lipase Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for Endothelial Lipase 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 Endothelial Lipase Antibody - BSA Free
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Protocols
View specific protocols for Endothelial Lipase Antibody - BSA Free (NB400-111):
Western Blot Procedure
1. Heat diluted samples at 70 degrees Celcius for 10 minutes.
2. Load samples onto a 10% Bis-Tris gel.
3. Run gel for ~45 minutes at 200V.
4. Transfer gel to PVDF membrane at 45V for ~90 minutes.
5. Block the membrane overnight at 4 degrees Celcius, in blocking buffer [PBS + 0.2% Tween-20 + 5% milk], gently shaking.
6. Rinse the membrane twice, quickly, in PBS-T.
7. Wash the membrane in PBS-T 3 times for 5 minutes, each.
8. Incubate the membrane with primary antibody [NB 400-111 or NB 400-118], diluted 1:500 in blocking buffer, for 1 hour at RT, gently shaking.
9. Rinse the membrane twice, quickly, in PBS-T.
10. Wash the membrane in PBS-T 3 times for 5 minutes, each.
11. Incubate the membrane with secondary antibody [NB 730-H], diluted 1:5,000 in blocking buffer, for 1 hour at RT, gently shaking.
12. Rinse the membrane twice, quickly, in PBS-T.
13. Wash the membrane in PBS-T 3 times for 5 minutes, each.
14. Detect protein using ECL, ~1 minute exposure.
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
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- 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 Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- 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 ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- 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
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- 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