NG2/MCSP Antibody (LHM 2) - Azide and BSA Free
Novus Biologicals | Catalog # NBP2-80873
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Scientific Data Images for NG2/MCSP Antibody (LHM 2) - Azide and BSA Free
Western Blot: NG2/MCSP Antibody (LHM 2)Azide and BSA Free [NBP2-80873]
Western Blot: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - Analysis of NG2 expression in HeLa whole cell lysate. Image from the standard format of this antibody.Immunohistochemistry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Immunohistochemistry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - Staining of NG2 in human brain using DAB with hematoxylin counterstain. Image from the standard format of this antibody.Flow Cytometry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Flow Cytometry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - Antibody was tested at 1:400 in MCF7 cells using an Alexa Fluor 488 secondary (shown in green) alongside unstained cells (shown in red). Image from the standard format of this antibody.Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - A cell surface stain was performed on U87MG cells with NG2/MCSP antibody (LHM 2) NB100-2688AF647 (blue) and a matched isotype control NBP2-27287AF647 (orange). Cells were incubated in an antibody dilution of 2 ug/mL for 20 minutes at room temperature. Both antibodies were directly conjugated to Alexa Fluor 647.Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - A cell surface stain was performed on U87MG cells with NG2/MCSP antibody (LHM 2) NB100-2688PCP (blue) and a matched isotype control NBP2-27287PCP (orange). Cells were incubated in an antibody dilution of 2.5 ug/mL for 20 minutes at room temperature. Both antibodies were directly conjugated to PerCP complex.Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Flow (Cell Surface): NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - A surface stain was performed on A375 Cells with NG2/MCSP (LHM2) antibody NB100-2688 (blue) and a matched isotype control NBP1-43319 (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems). Image from the standard format of this antibody.Flow Cytometry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Flow Cytometry: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - A cell surface stain was performed on SK-MEL-28 cells with NG2/MCSP antibody (LHM 2) NB100-2688AF700 (blue) and a matched isotype control (orange). Cells were incubated in an antibody dilution of 5 ug/mL for 20 minutes at room temperature. Both antibodies were directly conjugated to Alexa Fluor 700.Western Blot: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873]
Western Blot: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] - Western blot shows lysates of HeLa human cervical epithelial carcinoma parental cell line and NG2/MCSP (LHM2) knockout (KO) HeLa cell line. PVDF membrane was probed with 1.0 ug/ml of Mouse Anti-Human NG2/MCSP (LHM2) Polyclonal Antibody (Catalog # NB100-2688) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #HAF018). Specific band was detected for NG2/MCSP (LHM2) at approximately 300 kDa (as indicated) in the parental HeLa cell line, but is not detectable in the knockout HeLa cell line. This experiment was conducted under reducing conditions. Image from the standard format of this antibody.Western Blot: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] -
Differentiation of hASCs towards endothelial cells (ECs) in NFC hydrogel. (A) Differentiation of hASCs in 0.125% NFC hydrogel in endothelial growth medium for 21 days. Scale bars, 100 um (d1) and 50 um (d10, d21). (B) Differentiated cells in 0.125% NFC hydrogel on d7 showing branching of cellular structures (arrows). Scale bars, 25 um. (C) Western blot showing expression of endothelial specific marker CD31 and alpha-smooth muscle actin ( alpha -SMA) in hASCs vs. human umbilical vein endothelial cells (HUVEC) (n = 3, 1 technical replicate). (D) Western blot of pericyte marker NG2 in hASCs and HUVECs. (E) Quantification of NG2 expression (n = 3, 1 technical replicate). * p < 0.05. Ang-1, angiopoietin-1; diff., differentiated cells. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36289846), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: NG2/MCSP Antibody (LHM 2) - Azide and BSA Free [NBP2-80873] -
Differentiation of hASCs towards endothelial cells (ECs) in NFC hydrogel. (A) Differentiation of hASCs in 0.125% NFC hydrogel in endothelial growth medium for 21 days. Scale bars, 100 um (d1) and 50 um (d10, d21). (B) Differentiated cells in 0.125% NFC hydrogel on d7 showing branching of cellular structures (arrows). Scale bars, 25 um. (C) Western blot showing expression of endothelial specific marker CD31 and alpha-smooth muscle actin ( alpha -SMA) in hASCs vs. human umbilical vein endothelial cells (HUVEC) (n = 3, 1 technical replicate). (D) Western blot of pericyte marker NG2 in hASCs and HUVECs. (E) Quantification of NG2 expression (n = 3, 1 technical replicate). * p < 0.05. Ang-1, angiopoietin-1; diff., differentiated cells. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36289846), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for NG2/MCSP Antibody (LHM 2) - Azide and BSA Free
Flow (Cell Surface)
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Immunohistochemistry-Frozen
Immunohistochemistry-Paraffin
Immunoprecipitation
Western Blot
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Advanced Features
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- Antigen Density Selector - Match fluorochrome brightness with antigen density
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Background: NG2/MCSP
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Product Documents for NG2/MCSP Antibody (LHM 2) - Azide and BSA Free
Certificate of Analysis
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Product Specific Notices for NG2/MCSP Antibody (LHM 2) - 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.
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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
- 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
- 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
- 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
- Immunoprecipitation Protocol
- 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
- 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: 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