Lgr5/GPR49 Antibody - Azide and BSA Free
Novus Biologicals | Catalog # NLS1235
Key Product Details
Species Reactivity
Human
Applications
Immunohistochemistry, Immunohistochemistry-Paraffin
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
Format
Azide and BSA Free
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Product Specifications
Immunogen
Synthetic peptide [KLH conjugated] made to the 2nd cytoplasmic loop of human GPR49/LGR5. [UniProt# O75473]
Reactivity Notes
Immunogen sequence has 81% identity with mouse.
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Scientific Data Images for Lgr5/GPR49 Antibody - Azide and BSA Free
Immunohistochemistry-Paraffin: Lgr5/GPR49 Antibody - Azide and BSA Free [NLS1235]
Immunohistochemistry-Paraffin: Lgr5/GPR49 Antibody [NLS1235] - GPR49/LGR5 Antibody [NLS1235] - Staining of a FFPE section of human cortex.Immunohistochemistry: Lgr5/GPR49 Antibody - Azide and BSA Free [NLS1235]
Immunohistochemistry: Lgr5/GPR49 Antibody [NLS1235] - Stem cells, neutrophils and eosinophils in human bone marrow (1ug/ml).Applications for Lgr5/GPR49 Antibody - Azide and BSA Free
Application
Recommended Usage
Immunohistochemistry
5-8 ug/ml
Immunohistochemistry-Paraffin
5-8 ug/ml
Application Notes
This GPR49/LGR5 antibody is useful for Immunohistochemistry on paraffin sections.
Formulation, Preparation, and Storage
Purification
Immunogen affinity purified
Formulation
PBS
Format
Azide and BSA Free
Preservative
No Preservative
Concentration
1 mg/ml
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: Lgr5/GPR49
Long Name
Leucine-rich Repeat Containing G Protein-coupled Receptor 5
Alternate Names
FEX, GPR49, GPR67, HG38
Entrez Gene IDs
8549 (Human)
Gene Symbol
LGR5
UniProt
Additional Lgr5/GPR49 Products
Product Documents for Lgr5/GPR49 Antibody - Azide and BSA Free
Certificate of Analysis
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Product Specific Notices for Lgr5/GPR49 Antibody - Azide and 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.
Related Research Areas
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Protocols
View specific protocols for Lgr5/GPR49 Antibody - Azide and BSA Free (NLS1235):
Lgr5/GPR49 Antibody:
Immunohistochemistry
1. Prepare tissue with formalin fixation and by embedding it in paraffin wax.
2. Make 4-mm 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 5 minutes each @ RT.
5. Rehydrate the tissues by washing the slides in 3 changes of 100% alcohol 3 minutes each @ RT.
6. Wash the slides in 2 changes of 95% alcohol 3 minutes each @ RT.
7. Wash the slides in 1 change of 80% alcohol 3 minutes @ RT.
8. Rinse the slides in gentle running distilled water 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 20 minutes @ RT.
13. Drain protein block from the slides and apply the diluted primary antibody 45 minutes @ RT.
14. Rinse the slide in 1X TBS-T 1 minute @ RT.
15. Apply a biotinylated anti-rabbit IgG (H+L) secondary 30 minutes @ RT.
16. Rinse the slide in 1X TBS-T 1 minute @ RT.
17. Apply an alkaline phosphatase steptavidin 30 minutes @ RT.
18. Rinse the slide in 1X TBS-T 1 minute @ RT.
19. Apply an alkaline phosphatase chromagen substrate 30 minutes @ RT.
20. Rinse the slide in distilled water 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 1 minute each @ RT.
22. Wash the slides in 2 changes of 95% alcohol 1 minute each @ RT.
23. Wash the slides in 3 changes of 100% alcohol 1 minute each @ RT.
24. Wash the slides in 3 changes of xylene 1 minute each @ RT.
25. Apply cover slip.
Immunohistochemistry
1. Prepare tissue with formalin fixation and by embedding it in paraffin wax.
2. Make 4-mm 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 5 minutes each @ RT.
5. Rehydrate the tissues by washing the slides in 3 changes of 100% alcohol 3 minutes each @ RT.
6. Wash the slides in 2 changes of 95% alcohol 3 minutes each @ RT.
7. Wash the slides in 1 change of 80% alcohol 3 minutes @ RT.
8. Rinse the slides in gentle running distilled water 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 20 minutes @ RT.
13. Drain protein block from the slides and apply the diluted primary antibody 45 minutes @ RT.
14. Rinse the slide in 1X TBS-T 1 minute @ RT.
15. Apply a biotinylated anti-rabbit IgG (H+L) secondary 30 minutes @ RT.
16. Rinse the slide in 1X TBS-T 1 minute @ RT.
17. Apply an alkaline phosphatase steptavidin 30 minutes @ RT.
18. Rinse the slide in 1X TBS-T 1 minute @ RT.
19. Apply an alkaline phosphatase chromagen substrate 30 minutes @ RT.
20. Rinse the slide in distilled water 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 1 minute each @ RT.
22. Wash the slides in 2 changes of 95% alcohol 1 minute each @ RT.
23. Wash the slides in 3 changes of 100% alcohol 1 minute each @ RT.
24. Wash the slides in 3 changes of xylene 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