DARC Antibodies
We offer DARC Antibodies for use in common research applications: ELISA, Flow Cytometry, Immunocytochemistry, Immunohistochemistry, Immunohistochemistry-Paraffin, Peptide ELISA, Western Blot. Each DARC Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our DARC Antibodies can be used in a variety of model species: Human, Mouse, Rat. Use the list below to choose the DARC Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our DARC polyclonal antibodies and browse our DARC monoclonal antibody catalog.
Alternate Names for DARC Antibodies
anti-DARC antibody, anti-CCBP1 antibody, anti-CD234 antibody, anti-CD234 antigen antibody, anti-Dfy antibody, anti-Duffy antigen/chemokine receptor antibody, anti-Duffy blood group antigen antibody, anti-Duffy blood group, chemokine receptor antibody, anti-Fy glycoprotein antibody, anti-FYDuffy blood group antibody, anti-Glycoprotein D antibody, anti-GPDWBCQ1 antibody, anti-GpFy antibody, anti-Plasmodium vivax receptor antibody
11 Results for "darc" in Primary Antibodies
![Western Blot: DARC Antibody [NB100-2421] - DARC (0.3ug/ml) staining of Human Liver lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/DARC-Antibody-Western-Blot-NB100-2421-img0007.jpg "Western Blot: DARC Antibody [NB100-2421] - DARC (0.3ug/ml) staining of Human Liver lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: DARC Antibody [NB100-2421] - Staining of paraffin embedded Human Lung. Microwaved antigen retrieval with citrate buffer Ph 6, AP-staining.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NB100-2421-img0009.jpg)
![Flow Cytometry: DARC Antibody [NB100-2421] - analysis of paraformaldehyde fixed HEK293 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (0.4ug/ml). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/DARC-Antibody-Flow-Cytometry-NB100-2421-img0010.jpg)
![Immunohistochemistry-Paraffin: DARC Antibody [NB100-2421] - DARC (3ug/ml) staining of paraffin embedded human kidney. Microwaved antigen retrieval with citrate buffer pH 6, HRP-staining.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NB100-2421-img0008.jpg)
![Western Blot: DARC Antibody - BSA Free [NBP1-77278] - DARC Antibody [NBP1-77278] - DARC expression in monocytes is dependent on an IL-22/IL-22Ra1-STAT5b signaling axis. THP1 cells were incubated with 20 ng/mL IL-22 in the absence or presence of the indicated concentrations of the STAT5b inhibitor, CAS285989, for 24 h and DARC protein expression was determined by immunoblotting assay. Western blot was quantified and expressed as the ratio of DARC and beta-actin intensity. Data are representative of three independent experiments with similar results. Image collected and cropped by CiteAb from the following publication (www.mdpi.com/2073-4409/8/12/1587) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/DARC-Antibody-Western-Blot-NBP1-77278-img0005.jpg "<b>Biological Strategies Validation. </b>Western Blot: DARC Antibody - BSA Free [NBP1-77278] - DARC Antibody [NBP1-77278] - DARC expression in monocytes is dependent on an IL-22/IL-22Ra1-STAT5b signaling axis. THP1 cells were incubated with 20 ng/mL IL-22 in the absence or presence of the indicated concentrations of the STAT5b inhibitor, CAS285989, for 24 h and DARC protein expression was determined by immunoblotting assay. Western blot was quantified and expressed as the ratio of DARC and beta-actin intensity. Data are representative of three independent experiments with similar results. Image collected and cropped by CiteAb from the following publication (www.mdpi.com/2073-4409/8/12/1587) licensed under a CC-BY license.")
![<b>Biological Strategies Validation. </b>Western Blot: DARC Antibody - BSA Free [NBP1-77278] - DARC Antibody [NBP1-77278] - Analysis in human cerebellum tissue lysate with antibody at 1 ug/mL.](http://images.novusbio.com/fullsize/DARC-Antibody-Western-Blot-NBP1-77278-img0004.jpg)
![Immunohistochemistry: DARC Antibody - BSA Free [NBP1-77278] - Immunohistochemistry of DARC in mouse brain tissue with DARC antibody at 2.5 ug/mL.](http://images.novusbio.com/fullsize/nbp1-77278_rabbit-polyclonal-darc-antibody-2711202419553068.jpg)
![Western Blot: DARC Antibody (2C3) - Chimeric [NBP2-75197] - Western Blot using anti-DARC antibody 2C3 (Ab00893) Human liver lysate samples (35ug protein in RIPA buffer) were resolved on a 10% SDS PAGE gel and blots probed with the chimeric rabbit version of 2C3 (NBP2-75197) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence. The expected running size for DARC is 35.6kDa. NBP2-75197 successfully detected DARC in human liver lysate.](http://images.novusbio.com/fullsize/DARC-Antibody-2C3-Chimeric-Western-Blot-NBP2-75197-img0001.jpg "Western Blot: DARC Antibody (2C3) - Chimeric [NBP2-75197] - Western Blot using anti-DARC antibody 2C3 (Ab00893) Human liver lysate samples (35ug protein in RIPA buffer) were resolved on a 10% SDS PAGE gel and blots probed with the chimeric rabbit version of 2C3 (NBP2-75197) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence. The expected running size for DARC is 35.6kDa. NBP2-75197 successfully detected DARC in human liver lysate.")
![Immunocytochemistry /Immunofluorescence: DARC Antibody (2C3) - Chimeric - Azide and BSA Free [NBP2-75197] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on coverslips, permeabilized with 0.15% Triton and stained with NBP2-75197 at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing cytoplasmic staining, likely of endosomes, and some membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-75197, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp2-75197_rabbit-monoclonal-darc-antibody-2c3-chimeric-74202522113041.png)
![Western Blot: DARC Antibody (SR1582) [NBP3-21980] - Western blot analysis using NBP3-21980 in Human fetal liver lysate.](http://images.novusbio.com/fullsize/nbp3-21980_rabbit-darc-mab-sr1582-57202317215170.jpg "Western Blot: DARC Antibody (SR1582) [NBP3-21980] - Western blot analysis using NBP3-21980 in Human fetal liver lysate.")
![Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86587] - Staining in human smooth muscle and kidney tissues using anti-ACKR1 antibody. Corresponding ACKR1 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86587-img0006.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86587] - Staining in human smooth muscle and kidney tissues using anti-ACKR1 antibody. Corresponding ACKR1 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86587] - Staining of human smooth muscle shows high expression.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86587-img0005.jpg)
![Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86587] - Staining of human kidney shows low expression as expected.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86587-img0004.jpg)
![Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86586] - Staining in human smooth muscle and kidney tissues using anti-ACKR1 antibody. Corresponding ACKR1 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86586-img0006.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86586] - Staining in human smooth muscle and kidney tissues using anti-ACKR1 antibody. Corresponding ACKR1 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86586] - Staining of human smooth muscle shows high expression.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86586-img0005.jpg)
![Immunohistochemistry-Paraffin: DARC Antibody [NBP1-86586] - Staining of human kidney shows low expression as expected.](http://images.novusbio.com/fullsize/DARC-Antibody-Immunohistochemistry-Paraffin-NBP1-86586-img0004.jpg)
![Flow Cytometry: DARC Antibody (18B11) [NBP3-26634] - Overlay Peak curve showing 293 cells stained with DARC Antibody (18B11) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26634_rabbit-darc-mab-18b11-282202414183683.jpg "Flow Cytometry: DARC Antibody (18B11) [NBP3-26634] - Overlay Peak curve showing 293 cells stained with DARC Antibody (18B11) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.")