Human CXCR4 PE‑conjugated Antibody
R&D Systems | Catalog # FAB173P
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Scientific Data Images for Human CXCR4 PE‑conjugated Antibody
Detection of CXCR4 in Human Blood Lymphocytes by Flow Cytometry.
Human peripheral blood lymphocytes were stained with Mouse Anti-Human CXCR4 PE-conjugated Monoclonal Antibody (Catalog # FAB173P) and Mouse Anti-Human CD19 APC-conjugated Monoclonal Antibody (FAB4867A) for 15 minutes at 37°C followed by 15 minutes at room temperature. View our protocol for Staining Membrane-associated Proteins.Detection of CXCR4 by Flow Cytometry
Representative example of flow cytometry quantification of complexes neutrophil–CD41a+ (NPAs, neutrophil–platelet aggregates) and lymphocyte markers’ expression. (A) Neutrophil cluster identification (region R1) based on its low CD14 expression (FL3) and side-scattering (SSC) morphological characteristics. (B) The R1-based histogram’s subtraction analysis (positive events (continuous line) minus isotype control (dotted line)) was used to quantify both the percentage of complexes CD41a+ (grey events in M1) and their RFI (median of M1 histogram minus median of the isotype control). (C) Lymphocyte cluster identification based on its forward- (FSC) and side-scattering characteristics (region R1). (D) Representative quantification of lymphocyte CXCR4 expression following the overlay histogram’s subtraction analysis (see above). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36836785), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of CXCR4 by Flow Cytometry
Representative example of flow cytometry quantification of complexes neutrophil–CD41a+ (NPAs, neutrophil–platelet aggregates) and lymphocyte markers’ expression. (A) Neutrophil cluster identification (region R1) based on its low CD14 expression (FL3) and side-scattering (SSC) morphological characteristics. (B) The R1-based histogram’s subtraction analysis (positive events (continuous line) minus isotype control (dotted line)) was used to quantify both the percentage of complexes CD41a+ (grey events in M1) and their RFI (median of M1 histogram minus median of the isotype control). (C) Lymphocyte cluster identification based on its forward- (FSC) and side-scattering characteristics (region R1). (D) Representative quantification of lymphocyte CXCR4 expression following the overlay histogram’s subtraction analysis (see above). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36836785), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human CXCR4 PE‑conjugated Antibody
Flow Cytometry
Sample: Human peripheral blood lymphocytes
Reviewed Applications
Read 1 review rated 5 using FAB173P in the following applications:
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Formulation, Preparation, and Storage
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Stability & Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: CXCR4
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Additional CXCR4 Products
Product Documents for Human CXCR4 PE‑conjugated Antibody
Certificate of Analysis
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Product Specific Notices for Human CXCR4 PE‑conjugated Antibody
For research use only
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Citations for Human CXCR4 PE‑conjugated Antibody
Customer Reviews for Human CXCR4 PE‑conjugated Antibody (1)
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Application: Flow CytometrySample Tested: induced pluripotent stem cells and endodermSpecies: HumanVerified Customer | Posted 12/15/2016We use CXCR4 to test the % positive definitive endoderm made from human induced pluripotent stem cells.
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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- Flow Cytometry Troubleshooting Guide
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- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- View all Protocols, Troubleshooting, Illustrated assays and Webinars