Ulex Europaeus Lectin 1 Antibody
Novus Biologicals | Catalog # NB110-13922
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Key Product Details
Species Reactivity
Validated:
Plant
Cited:
Mouse
Applications
Validated:
Immunohistochemistry, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen, Immunocytochemistry/ Immunofluorescence
Cited:
IF/IHC
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
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Product Specifications
Immunogen
Anti-Ulex Europaeus-I (UEA-I) Lectin is developed in rabbit using purified Ulex Europaeus-I lectin from gorse seeds as the immunogen.
Marker
Endothelial Cells
Specificity
The antibody may be used for studies of the vascular structures. It reacts specifically with UEA-I bound to human endothelial cells of normal and neoplastic blood and lymphatic vessels. Its uniform reaction with vessels enables differentation between vessels and artificial slits in the tissue.
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Scientific Data Images for Ulex Europaeus Lectin 1 Antibody
Immunohistochemistry: Ulex Europaeus Lectin 1 Antibody [NB110-13922]
Immunohistochemistry: Ulex Europaeus Lectin 1 Antibody [NB110-13922] - Formalin fixed, paraffin-embedded Human tonsil tissue sections were stained with 1:1000 Anti-Lectin, Ulex europaeus-I antibody produced in Rabbit followed by 1:30 Anti-Rabbit IgG (whole molecule)-FITC antibody produced in Goat.Applications for Ulex Europaeus Lectin 1 Antibody
Application
Recommended Usage
Immunocytochemistry/ Immunofluorescence
1:500
Immunohistochemistry-Frozen
1:500
Immunohistochemistry-Paraffin
1:500
Application Notes
Lectin isolated from Ulex europaeus I (NBP2-42700) is specific for alpha-L-fucose-containing glycocompounds which (in combination with NB110-13922) makes it a specific marker for vascular endothelial cells and tumors derived from them. For immunoassays on animal tissues, Ulex Europaeus Lectin 1 Protein (NBP2-42700) would be a required product alongwith NB110-13922. Technically, NBP2-42700 will bind the carbohydrate moiety on vascular endothelial cells as first primary reagent and then NB110-13922 will bind to Ulex Europaeus-1 lectin (NBP2-42700) in the primary antibody incubation step (See product specific IHC-P Protocol).
Formulation, Preparation, and Storage
Purification
Unpurified
Formulation
Whole antisera, delipidized
Preservative
0.09% Sodium Azide
Concentration
This product is unpurified. The exact concentration of antibody is not quantifiable.
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Background: Ulex Europaeus Lectin 1
Alternate Names
Gorse or Furze Lectin, UEA-1; H(O) lectin 1; Anti H(O) lectin I
Additional Ulex Europaeus Lectin 1 Products
Product Documents for Ulex Europaeus Lectin 1 Antibody
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for Ulex Europaeus Lectin 1 Antibody
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 Ulex Europaeus Lectin 1 Antibody
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Protocols
View specific protocols for Ulex Europaeus Lectin 1 Antibody (NB110-13922):
Immunohistochemistry protocol for Ulex Europaeus Lectin 1 Antibody (NB110-13922):
IHC Staining Protocol
Materials:
1. Paraffin sections (4-6um) of animal or human tissue (material fixed with 10% phosphate buffered formalin)
2. Phosphate buffered saline (PBS) pH 7.5-7.6 (10-20 mM) containing 1% BSA
3. 0.1% Pronase in PBS
4. 0.1% Trypsin in PBS
5. 10 ug/ml Ulex Europaeus-1 lectin (NBP2-42700)
6. Anti Ulex Europaeus-1 lectin antibody (NB110-13922)
7. Secondary antiserum: FITC anti-rabbit IgG (H+L)
8. Mounting Medium
Method:
1. After deparaffinization treat with 0.1% Promase in PBS for 10 minutes at 37C. Alternatively, digest with 0.1% Trypsin in PBS for 25 minutes at 37C. Gently rinse in PBS for 5 minutes (2X).
2. Apply 2 drops of 10 ug/ml solution of UEA-1 (NBP2-42700)
3. Incubate for 30 minutes at 37C. Gently rinse in PBS for 5 minutes (X2)
4. Apply 2 drops Anti Ulex Europaeus-1 lectin antibody (NB110-13922) diluted 1:500 in PBS containing 1% BSA
5. Incubate for 1 hr. at 37C
6. Gently rinse in PBS for 5 minutes
7. Drain, carefully blot away excess moisture around the sections.
8. Quickly apply freshly prepared diluted FITC secondary antiserum (at previously determined appropriate dilution) in PBS containing 1% BSA.
9. Incubate for 30 minutes at 37C
10. Gently rinse in PBS for 5 minutes (x2). Blot away excess moisture from around the sections.
11. Add mounting medium and coverslip.
12. Read under the UV fluorescent microscope. Mounted preparations can be stored in a refrigerator.
Notes:
1. Do not allow tissue sections to dry out at any time during the aforementioned procedure.
2. In case of excessive background staining remove aggregates from antisera by centrifuging for 15 minutes immediately prior to use.
IHC Staining Protocol
Materials:
1. Paraffin sections (4-6um) of animal or human tissue (material fixed with 10% phosphate buffered formalin)
2. Phosphate buffered saline (PBS) pH 7.5-7.6 (10-20 mM) containing 1% BSA
3. 0.1% Pronase in PBS
4. 0.1% Trypsin in PBS
5. 10 ug/ml Ulex Europaeus-1 lectin (NBP2-42700)
6. Anti Ulex Europaeus-1 lectin antibody (NB110-13922)
7. Secondary antiserum: FITC anti-rabbit IgG (H+L)
8. Mounting Medium
Method:
1. After deparaffinization treat with 0.1% Promase in PBS for 10 minutes at 37C. Alternatively, digest with 0.1% Trypsin in PBS for 25 minutes at 37C. Gently rinse in PBS for 5 minutes (2X).
2. Apply 2 drops of 10 ug/ml solution of UEA-1 (NBP2-42700)
3. Incubate for 30 minutes at 37C. Gently rinse in PBS for 5 minutes (X2)
4. Apply 2 drops Anti Ulex Europaeus-1 lectin antibody (NB110-13922) diluted 1:500 in PBS containing 1% BSA
5. Incubate for 1 hr. at 37C
6. Gently rinse in PBS for 5 minutes
7. Drain, carefully blot away excess moisture around the sections.
8. Quickly apply freshly prepared diluted FITC secondary antiserum (at previously determined appropriate dilution) in PBS containing 1% BSA.
9. Incubate for 30 minutes at 37C
10. Gently rinse in PBS for 5 minutes (x2). Blot away excess moisture from around the sections.
11. Add mounting medium and coverslip.
12. Read under the UV fluorescent microscope. Mounted preparations can be stored in a refrigerator.
Notes:
1. Do not allow tissue sections to dry out at any time during the aforementioned procedure.
2. In case of excessive background staining remove aggregates from antisera by centrifuging for 15 minutes immediately prior to use.
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
- 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
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