Neuromedin BR/NMBR Antibody - BSA Free
Novus Biologicals | Catalog # NLS825
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Scientific Data Images for Neuromedin BR/NMBR Antibody - BSA Free
Immunohistochemistry-Paraffin: Neuromedin BR/NMBR Antibody - BSA Free [NLS825]
Immunohistochemistry-Paraffin: Neuromedin B R/NMBR Antibody [NLS825] - Human lung, carcinoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval dilution 16 ug/ml.Immunohistochemistry-Paraffin: Neuromedin BR/NMBR Antibody - BSA Free [NLS825]
Immunohistochemistry-Paraffin: Neuromedin B R/NMBR Antibody [NLS825] - Analysis of anti-NMBR antibody with human brain olfactory bulb.Immunohistochemistry-Paraffin: Neuromedin BR/NMBR Antibody - BSA Free [NLS825]
Immunohistochemistry-Paraffin: Neuromedin B R/NMBR Antibody [NLS825] - Analysis of anti-NMBR antibody with human brain, glioblastoma.Immunohistochemistry-Paraffin: Neuromedin BR/NMBR Antibody - BSA Free [NLS825]
Immunohistochemistry-Paraffin: Neuromedin B R/NMBR Antibody [NLS825] - Human Skin, Melanoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.Immunohistochemistry-Paraffin: Neuromedin BR/NMBR Antibody - BSA Free [NLS825]
Immunohistochemistry-Paraffin: Neuromedin B R/NMBR Antibody [NLS825] - Human testis. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Dilution 16 ug/ml.Applications for Neuromedin BR/NMBR Antibody - BSA Free
Immunohistochemistry-Paraffin
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Background: Neuromedin BR/NMBR
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Product Specific Notices for Neuromedin BR/NMBR 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.
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Protocols
View specific protocols for Neuromedin BR/NMBR Antibody - BSA Free (NLS825):
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 at 60 degrees Celcius.
4. Deparaffinize the tissues by wash drying the slides in 3 changes of xylene approximately 5 minutes each @ RT.
5. Rehydrate the tissues by washing the slides in 3 changes of 100% alcohol approximately 3 minutes each @ RT.
6. Wash the slides in 2 changes of 95% alcohol approximately 3 minutes each @ RT.
7. Wash the slides in 1 change of 80% alcohol approximately 3 minutes @ RT.
8. Rinse the slides in gentle running distilled water approximately 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 approximately 20 minutes @ RT.
13. Drain protein block from the slides and apply the diluted primary antibody approximately 45 minutes @ RT.
14. Rinse the slide in 1X TBS-T approximately 1 minute @ RT.
15. Apply a biotinylated anti-rabbit IgG (H+L) secondary approximately 30 minutes @ RT.
16. Rinse the slide in 1X TBS-T approximately 1 minute at RT.
17. Apply an alkaline phosphatase steptavidin approximately 30 minutes at RT.
18. Rinse the slide in 1X TBS-T approximately 1 minute at RT.
19. Apply an alkaline phosphatase chromagen substrate approximately 30 minutes at RT.
20. Rinse the slide in distilled water approximately 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 approximately 1 minute each @ RT.
22. Wash the slides in 2 changes of 95% alcohol approximately 1 minute each @ RT.
23. Wash the slides in 3 changes of 100% alcohol approximately 1 minute each @ RT.
24. Wash the slides in 3 changes of xyleneapproximately 1 minute each @ RT.
25. Apply cover slip.
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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- IHC Sample Preparation (Frozen sections vs Paraffin)
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- Preparing Samples for IHC/ICC Experiments
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- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
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- 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
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
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- View all Protocols, Troubleshooting, Illustrated assays and Webinars