TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
Novus Biologicals | Catalog # NB100-56512
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Key Product Details
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Product Specifications
Immunogen
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Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
Immunohistochemistry: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512]
TRANCE-TNFSF11-RANK-L-Antibody-12A668-Immunohistochemistry-NB100-56512-img0019.jpgWestern Blot: TRANCE/TNFSF11/RANK L Antibody (12A668)BSA Free [NB100-56512]
Western Blot: TRANCE/TNFSF11/RANK L Antibody (12A668) [NB100-56512] - Analysis using Azide Free version of NB100-56512. Human lymph node lysate (35ug per lane, RIPA buffer). Band detected at ~35kDa and ~28kDa. (Expected MW of 35.5kDa according to NP_003692.1 and of 27.7kDa according to NP_143026.1)Immunocytochemistry/ Immunofluorescence: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512]
Immunocytochemistry/Immunofluorescence: TRANCE/TNFSF11/RANK L Antibody (12A668) [NB100-56512] - TRANCE was detected in immersion fixed mouse splenocytes using anti-human/mouse/rat mouse monoclonal antibody (Catalog # NB100-56512) for 1 hour at room temperature. Cells were stained using NL557 (red) fluorescent anti-mouse secondary antibodies (Catalog # NL007) and counterstained with DAPI (blue).Immunohistochemistry: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512]
TRANCE-TNFSF11-RANK-L-Antibody-12A668-Immunohistochemistry-NB100-56512-img0020.jpgWestern Blot: TRANCE/TNFSF11/RANK L Antibody (12A668)BSA Free [NB100-56512]
Western Blot: TRANCE/TNFSF11/RANK L Antibody (12A668) [NB100-56512] - Analysis of transfected cell lysate was probed with TRANCE/TNFSF11/RANK L antibody.Immunohistochemistry-Paraffin: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512]
Immunohistochemistry-Paraffin: TRANCE/TNFSF11/RANK L Antibody (12A668) [NB100-56512] - Analysis using Azide Free version of NB100-56512. FFPE human liver stained with TRANCE/TNFSF11/RANK L antibody, peroxidase-conjugate and DAB chromogen. A 2 hr incubation at RT was used.Immunohistochemistry-Paraffin: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512]
Immunohistochemistry-Paraffin: TRANCE/TNFSF11/RANK L Antibody (12A668) [NB100-56512] - Analysis using Azide Free version of NB100-56512. FFPE human lymph node probed with TRANCE/TNFSF11/RANK L antibody.Immunohistochemistry: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512] -
MQDL detects EMT biomarkers in clinical bone tissue specimens.A representative specimen of human prostate cancer bone metastasis co-expressed high levels of epithelial EpCAM, and mesenchymal RANKL and vimentin proteins. ×400.Immunocytochemistry/ Immunofluorescence: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512] -
Immunocytochemistry/ Immunofluorescence: TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free [NB100-56512] - MQDL detects EMT biomarkers in clinical bone tissue specimens.A representative specimen of human prostate cancer bone metastasis co-expressed high levels of epithelial EpCAM, & mesenchymal RANKL & vimentin proteins. ×400. Image collected & cropped by CiteAb from the following publication (https://dx.plos.org/10.1371/journal.pone.0028670), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
Chromatin Immunoprecipitation (ChIP)
ELISA
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Immunohistochemistry-Paraffin
Western Blot
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
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Background: TRANCE/TNFSF11/RANK L
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Additional TRANCE/TNFSF11/RANK L Products
Product Documents for TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
Certificate of Analysis
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Product Specific Notices for TRANCE/TNFSF11/RANK L Antibody (12A668) - 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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Citations for TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ChIP Protocol Video
- Chromatin Immunoprecipitation (ChIP) Protocol
- Chromatin Immunoprecipitation Protocol
- 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
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- 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
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- 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
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- 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
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- 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
FAQs for TRANCE/TNFSF11/RANK L Antibody (12A668) - BSA Free
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Q: Does your RANKL antibody (NB100-56512, Clone 12A668) block the ligand binding site? (or what the epitope range is?) Furthermore, can this antibody use as agonistic?
A: This antibody was raised against a bacterially expressed fusion protein containing amino acid residues 1-317 / whole sequence of mouse TRANCE was used as immunogen (NP_003692; uniprot site). We have not epitope mapped this antibody and accordingly, we are not sure where on RANKL does this antibody bind. We are not aware of its use as agonist or antigonist but since this antibody worked really well in Flow, ICC/IF and IHC-P (applications wherein the antibody binds the antigen in more of native state), it is quite possible that it may work for functional application under in-vitro or in-vivo conditions.
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Q: I need a positive control in order to establish them for IHC-P. Do you have any further recommendations except the ones stated on the website. For example what kind of tissue could be used as a positive control?
A: RANK/TNFRSF11A demonstrates ubiquitous expression with high levels found in skeletal muscle, thymus, liver, colon, small intestine and adrenal gland. You may use any of these tissues as positive controls. For additional options, you may refer to the staining results posted at Human Protein atlas database and in some IHC-P related publications at online product sheet.
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Q: We have received a customer inquiry regarding your RANKL Antibody (12A668) 0.1mg, Cat # NB100-56512 (previously from Imgenex). Specifically, they would like to know if this product is suitable for use in immunoprecipitation, also, what is the level of cross reactivity to mouse compared to the target reactivity?
A: This product has been validated in mouse, so it is 100% guaranteed for use on mouse samples. It has never been directly tested by Novus or Imgenex for IP, but it works in ICC and for surface staining in Flow Cytometry. Because of this, I would expect that it would be suitable for use in IP as well.
-
Q: Does your RANKL antibody (NB100-56512, Clone 12A668) block the ligand binding site? (or what the epitope range is?) Furthermore, can this antibody use as agonistic?
A: This antibody was raised against a bacterially expressed fusion protein containing amino acid residues 1-317 / whole sequence of mouse TRANCE was used as immunogen (NP_003692; uniprot site). We have not epitope mapped this antibody and accordingly, we are not sure where on RANKL does this antibody bind. We are not aware of its use as agonist or antigonist but since this antibody worked really well in Flow, ICC/IF and IHC-P (applications wherein the antibody binds the antigen in more of native state), it is quite possible that it may work for functional application under in-vitro or in-vivo conditions.
-
Q: I need a positive control in order to establish them for IHC-P. Do you have any further recommendations except the ones stated on the website. For example what kind of tissue could be used as a positive control?
A: RANK/TNFRSF11A demonstrates ubiquitous expression with high levels found in skeletal muscle, thymus, liver, colon, small intestine and adrenal gland. You may use any of these tissues as positive controls. For additional options, you may refer to the staining results posted at Human Protein atlas database and in some IHC-P related publications at online product sheet.
-
Q: We have received a customer inquiry regarding your RANKL Antibody (12A668) 0.1mg, Cat # NB100-56512 (previously from Imgenex). Specifically, they would like to know if this product is suitable for use in immunoprecipitation, also, what is the level of cross reactivity to mouse compared to the target reactivity?
A: This product has been validated in mouse, so it is 100% guaranteed for use on mouse samples. It has never been directly tested by Novus or Imgenex for IP, but it works in ICC and for surface staining in Flow Cytometry. Because of this, I would expect that it would be suitable for use in IP as well.
-
Q: Does your RANKL antibody (NB100-56512, Clone 12A668) block the ligand binding site? (or what the epitope range is?) Furthermore, can this antibody use as agonistic?
A: This antibody was raised against a bacterially expressed fusion protein containing amino acid residues 1-317 / whole sequence of mouse TRANCE was used as immunogen (NP_003692; uniprot site). We have not epitope mapped this antibody and accordingly, we are not sure where on RANKL does this antibody bind. We are not aware of its use as agonist or antigonist but since this antibody worked really well in Flow, ICC/IF and IHC-P (applications wherein the antibody binds the antigen in more of native state), it is quite possible that it may work for functional application under in-vitro or in-vivo conditions.
-
Q: I need a positive control in order to establish them for IHC-P. Do you have any further recommendations except the ones stated on the website. For example what kind of tissue could be used as a positive control?
A: RANK/TNFRSF11A demonstrates ubiquitous expression with high levels found in skeletal muscle, thymus, liver, colon, small intestine and adrenal gland. You may use any of these tissues as positive controls. For additional options, you may refer to the staining results posted at Human Protein atlas database and in some IHC-P related publications at online product sheet.
-
Q: We have received a customer inquiry regarding your RANKL Antibody (12A668) 0.1mg, Cat # NB100-56512 (previously from Imgenex). Specifically, they would like to know if this product is suitable for use in immunoprecipitation, also, what is the level of cross reactivity to mouse compared to the target reactivity?
A: This product has been validated in mouse, so it is 100% guaranteed for use on mouse samples. It has never been directly tested by Novus or Imgenex for IP, but it works in ICC and for surface staining in Flow Cytometry. Because of this, I would expect that it would be suitable for use in IP as well.