Anti-CXCR7 antibody(DMC443); IgG1 Chimeric mAb
Figure 1. Flow cytometry analysis with Anti-CXCR7 (DMC443) on Expi293 cells transfected with human CXCR7 (Blue histogram) or Expi293 transfected with irrelevant protein (Red histogram).
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| Amount : | 100 µg |
| Isotype : | Rabbit/Human Fc chimeric IgG1 |
| Purification : | Purified from cell culture supernatant by affinity chromatography |
| Content : | Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8% trehalose is added as protectants before lyophilization. Please see Certificate of Analysis for specific instructions of reconstitution. |
| Storage condition : | Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature. |
| Uniprot ID : | P25106 |
| Alternative Name : | Atypical chemokine receptor 3;CXC-R7;CXCR-7;Chemokine orphan receptor 1;G-protein coupled receptor 159;RDC-1 |
Description :Anti-CXCR7 antibody(DMC443); IgG1 Chimeric mAb
This gene encodes a member of the G-protein coupled receptor family. Although this protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP); it is now considered to be an orphan receptor; in that its endogenous ligand has not been identified. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas.
This gene encodes a member of the G-protein coupled receptor family. Although this protein was earlier thought to be a receptor for vasoactive intestinal peptide (VIP); it is now considered to be an orphan receptor; in that its endogenous ligand has not been identified. The protein is also a coreceptor for human immunodeficiency viruses (HIV). Translocations involving this gene and HMGA2 on chromosome 12 have been observed in lipomas.
FACS 1:100
For Research Use Only. Not for use in diagnostic/therapeutics procedures.
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