| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12083-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26685-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21980-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48032 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-43338-0.5mg | |||
| BSA Free | NBP1-43338-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-66539-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-61697-0.025ml | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| FITC | NB500-622-100Tests | |||
| PE | NBP1-41282 | |||
![Immunohistochemistry-Paraffin: XCR1/CCXCR1 Antibody - BSA Free [NBP1-02343] - Human spleen tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/XCR1-CCXCR1-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NBP1-02343-img0002.jpg "Immunohistochemistry-Paraffin: XCR1/CCXCR1 Antibody - BSA Free [NBP1-02343] - Human spleen tissue after heat-induced antigen retrieval.")
![Immunocytochemistry/Immunofluorescence: Complement Component C5aR1 Antibody (S5/1) - Chimeric [NBP3-12083] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version S5/1 (NBP3-12083) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12083, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/Complement-Component-C5aR1-Antibody-S5-1-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12083-img0001.jpg "Immunocytochemistry/Immunofluorescence: Complement Component C5aR1 Antibody (S5/1) - Chimeric [NBP3-12083] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version S5/1 (NBP3-12083) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12083, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.")
![Immunoprecipitation: CCR9 Antibody (4G2) [NBP3-26685] - Immunoprecipitating CCR9 in HL-60 whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26685 in HL-60 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26685 (3ug) + HL-60 whole cell lysate (500ug). Lane 3: HL-60 whole cell lysate (20ug).](http://images.novusbio.com/fullsize/nbp3-26685_rabbit-ccr9-mab-4g2-262202413221517.jpg "Immunoprecipitation: CCR9 Antibody (4G2) [NBP3-26685] - Immunoprecipitating CCR9 in HL-60 whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26685 in HL-60 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26685 (3ug) + HL-60 whole cell lysate (500ug). Lane 3: HL-60 whole cell lysate (20ug).")
![Western Blot: CCR9 Antibody (4G2) [NBP3-26685] - Positive Western Blot detected in: SH-SY5Y whole cell lysate, HepG2 whole cell lysate, Jurkat whole cell lysate, HL-60 whole cell lysate, Hela whole cell lysate, U87 whole cell lysate, Mouse brain tissue. All lanes: CCR9 Antibody at 1ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 43, 41 KDa Observed band size: 43 KDa](http://images.novusbio.com/fullsize/nbp3-26685_rabbit-ccr9-mab-4g2-282202411472120.jpg)
![Immunocytochemistry/Immunofluorescence: CCR9 Antibody (4G2) [NBP3-26685] - Staining of HepG2 cells with CCR9 Antibody (4G2) at 1:33, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26685_rabbit-ccr9-mab-4g2-28220241312217.jpg)
![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: CXCR2/IL-8 RB Antibody (5E8-C7-F10) [NBP1-43338] - CXCR2positive breast cancer cells in the human brain. CXCR2-red fluorochrome, nucleus-DAPI. Antibody used at dilution of 1:100. This image was submitted via customer Review.](http://images.novusbio.com/fullsize/CXCR2-IL-8-RB-Antibody-5E8-C7-F10-Immunohistochemistry-Paraffin-NBP1-43338-img0005.jpg "Immunohistochemistry-Paraffin: CXCR2/IL-8 RB Antibody (5E8-C7-F10) [NBP1-43338] - CXCR2positive breast cancer cells in the human brain. CXCR2-red fluorochrome, nucleus-DAPI. Antibody used at dilution of 1:100. This image was submitted via customer Review.")
![Flow Cytometry: CXCR2/IL-8 RB Antibody (5E8-C7-F10) [NBP1-43338] - Analysis using the PE conjugate of NBP1-43338. Staining of normal human peripheral blood cells with Anti-Human CD4 APC (left) or Anti-Human CD56 (NCAM) APC (right) and Anti-Human CD182 (CXCR2) PE. Cells in the lymphocyte gate were used for analysis.](http://images.novusbio.com/fullsize/CXCR2-IL-8-RB-Antibody-5E8-C7-F10-Flow-Cytometry-NBP1-43338-img0004.jpg)
![Flow Cytometry: CXCR2/IL-8 RB Antibody (5E8-C7-F10) [NBP1-43338] - Staining of normal human peripheral blood cells with 0.25 ug of Mouse IgG1 kappa Isotype Control Purified (left) or 0.25 ug of Anti-Human CD182 (CXCR2) Purified (right) followed by F(ab')2 Anti-Mouse IgG PE . Cells in the large scatter population were used for analysis.](http://images.novusbio.com/fullsize/CXCR2-IL-8-RB-Antibody-5E8-C7-F10-Flow-Cytometry-NBP1-43338-img0002.jpg)
![Flow Cytometry: Complement Component C5a R1 Antibody (P12/1) [NB100-66539] - Staining of human peripheral blood granulocytes with MOUSE ANTI HUMAN CD88 (NB100-66539).](http://images.novusbio.com/fullsize/Complement-Component-C5a-R1-Antibody-P12-1-Flow-Cytometry-NB100-66539-img0001.jpg "Flow Cytometry: Complement Component C5a R1 Antibody (P12/1) [NB100-66539] - Staining of human peripheral blood granulocytes with MOUSE ANTI HUMAN CD88 (NB100-66539).")
![Flow Cytometry: Complement Component C5a R1 Antibody (P12/1) [NB100-66539] - Staining of human peripheral blood granulocytes with MOUSE ANTI HUMAN CD88: FITC.](http://images.novusbio.com/fullsize/Complement-Component-C5a-R1-Antibody-P12-1-Flow-Cytometry-NB100-66539-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: MEFV Antibody [NB600-809] - Immunofluorescence analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nuclear staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/MEFV-Antibody-Immunocytochemistry-Immunofluorescence-NB600-809-img0001.jpg "Immunocytochemistry/Immunofluorescence: MEFV Antibody [NB600-809] - Immunofluorescence analysis of paraformaldehyde fixed A431 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nuclear staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).")
![Flow Cytometry: MEFV Antibody [NB600-809] - Flow cytometric analysis of paraformaldehyde fixed A431 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (1 ug/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/MEFV-Antibody-Flow-Cytometry-NB600-809-img0002.jpg)
![Western Blot: CCR1 Antibody (8E10G6) [NBP2-61697] - Analysis using CD191 mAb against human CD191 (AA: extra mix) recombinant protein. (Expected MW is 37 kDa)](http://images.novusbio.com/fullsize/CCR1-Antibody-8E10G6-Western-Blot-NBP2-61697-img0003.jpg "Western Blot: CCR1 Antibody (8E10G6) [NBP2-61697] - Analysis using CD191 mAb against human CD191 (AA: extra mix) recombinant protein. (Expected MW is 37 kDa)")
![Flow Cytometry: CCR1 Antibody (8E10G6) [NBP2-61697] - Analysis of Ramos cells using CD191 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/CCR1-Antibody-8E10G6-Flow-Cytometry-NBP2-61697-img0002.jpg)
![Western Blot: CCR1 Antibody (8E10G6) [NBP2-61697] - Analysis using CD191 mAb against HEK293 (1) and CD191 (AA: extra mix)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/CCR1-Antibody-8E10G6-Western-Blot-NBP2-61697-img0004.jpg)
![ELISA: CCR1 Antibody (8E10G6) [NBP2-61697] - Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)](http://images.novusbio.com/fullsize/CCR1-Antibody-8E10G6-ELISA-NBP2-61697-img0001.jpg)
![Flow Cytometry: CD99 Antibody (MEM-131) [NB500-403] - Analysis using the FITC conjugate of NB500-403. Staining of Human peripheral blood lymphocytes with HCD99 FITC.](http://images.novusbio.com/fullsize/CD99-Antibody-MEM-131-Flow-Cytometry-NB500-403-img0004.jpg "Flow Cytometry: CD99 Antibody (MEM-131) [NB500-403] - Analysis using the FITC conjugate of NB500-403. Staining of Human peripheral blood lymphocytes with HCD99 FITC.")
![Flow Cytometry: CD99 Antibody (MEM-131) [NB500-403] - Analysis using the Biotin conjugate of NB500-403. Staining of Human peripheral blood lymphocytes biotinylated HCD99, followed by Sav-PE.](http://images.novusbio.com/fullsize/CD99-Antibody-MEM-131-Flow-Cytometry-NB500-403-img0003.jpg)
![Immunohistochemistry-Paraffin: CCR8 Antibody [NLS3847] - Brain Pituitary Pars Anterior](http://images.novusbio.com/fullsize/CCR8-Antibody-Immunohistochemistry-Paraffin-NLS3847-img0005.jpg "Immunohistochemistry-Paraffin: CCR8 Antibody [NLS3847] - Brain Pituitary Pars Anterior")
![Immunohistochemistry-Paraffin: CCR8 Antibody [NLS3847] - Analysis of anti-CCR8 antibody with tonsil, germinal center at 22 ug/ ml.](http://images.novusbio.com/fullsize/CCR8-Antibody-Immunohistochemistry-Paraffin-NLS3847-img0003.jpg)
![Immunohistochemistry-Paraffin: CCR8 Antibody [NLS3847] - Analysis of anti-CCR8 antibody with human lymph node, non-Hodgkins lymphoma.](http://images.novusbio.com/fullsize/CCR8-Antibody-Immunohistochemistry-Paraffin-NLS3847-img0004.jpg)
![Western Blot: CCR8 Antibody (JE31-99) [NBP3-32117] - Western blot analysis of CCR8 on mouse thymus tissue lysates with Rabbit anti-CCR8 antibody (NBP3-32117) at 1/1,000 dilution. Lysates/proteins at 30 ug/Lane. Predicted band size: 41 kDa Observed band size: 48 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32117) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32117_rabbit-ccr8-mab-je31-99-278202415295512.jpg "Western Blot: CCR8 Antibody (JE31-99) [NBP3-32117] - Western blot analysis of CCR8 on mouse thymus tissue lysates with Rabbit anti-CCR8 antibody (NBP3-32117) at 1/1,000 dilution. Lysates/proteins at 30 ug/Lane. Predicted band size: 41 kDa Observed band size: 48 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32117) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: CCR8 Antibody (JE31-99) [NBP3-32117] - Immunocytochemistry analysis of Raji cells labeling CCR8 with Rabbit anti-CCR8 antibody (NBP3-32117) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CCR8 antibody (NBP3-32117) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.](http://images.novusbio.com/fullsize/nbp3-32117_rabbit-ccr8-mab-je31-99-2920241192314.jpg)