Flow Cytometry, Extracellular: HEK-293F cells transiently transfected with human CXCR7 were stained with CXCR7 Monoclonal Antibody (CSB0095) (green) or isotype control antibody (gray), followed by AlexaFluor 647- conjugated anti-Mouse IgG secondary antibody. HEK-293F cells transiently transfected with an empty control vector were also stained with CXCR7 Monoclonal Antibody (CSB0095) (blue).

Flow Cytometry, Extracellular: HEK-293F cells transiently transfected with human CXCR7 were stained with CXCR7 Monoclonal Antibody (CSB0095) (green) or isotype control antibody (gray), followed by AlexaFluor 647- conjugated anti-Mouse IgG secondary antibody. HEK-293F cells transiently transfected with an empty control vector were also stained with CXCR7 Monoclonal Antibody (CSB0095) (blue).

CXCR7 MAb - CSB0095

Catalog #: CSB0095
Applications: FC   IF   ICC   ELISA   WB  
Isotype: IgG2a
Reactivity: Human (Others untested)
Extracellular epitope: Yes
Concentration: 1 mg/ml
Size: 100 µg
Fixative Compatibility: Paraformaldehyde (4%)
Detergent Compatibility: Triton X-100 (0.1%)
Technical Data Sheet
Safety Data Sheet
$475.00
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  • Description
Description

CSB VeRSaMAbs:
We produce and validate all our monoclonal antibodies in-house so that you can confidently choose the right antibody for your assay. All antibodies are VALIDATED for common applications, RECOMBINANT for batch-to-batch consistency, and SPECIFIC in binding to only your target.

Target CXCR7
Target Aliases ACKR3, GPR159, RDC1, CMKOR1, CXC-R7, CXCR-7, RDC-1
Isotype IgG2a
Species Reactivity Human (Others untested)
Concentration 1 mg/ml

Stable for 12 months from date of receipt when stored at 4°C. Avoid repeated freeze-thaw cycles.

CXCR7 is a multi-pass transmembrane protein, atypical chemokine receptor, and member of the G-protein coupled receptor family. CXCR7 is a receptor for CXCL11 and CXCL12/SDF1 and a coreceptor for HIV. CXCR7 is involved in chemokine responsiveness in migrating interneurons, resistance to apoptosis in glioma cells, cell adhesion and migration in malignant hematopoietic cells, axon guidance in the oculomotor system, and heart valve development.

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