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![Immunocytochemistry/Immunofluorescence: CLEC16A Antibody [NBP2-78807] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells, permeabilized with 0.15% Triton. Primary antibody incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing strong nuclear and weak cytoplasmic 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/CLEC16A-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-78807-img0001.jpg "Immunocytochemistry/Immunofluorescence: CLEC16A Antibody [NBP2-78807] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells, permeabilized with 0.15% Triton. Primary antibody incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing strong nuclear and weak cytoplasmic 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: CLEC16A Antibody [NBP2-78807] - Flow cytometric analysis of paraformaldehyde fixed A549 cells (blue line), permeabilized with 0.5% Triton. Primary antibody 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/CLEC16A-Antibody-Flow-Cytometry-NBP2-78807-img0002.jpg)
![Immunohistochemistry-Paraffin: CCR1 Antibody [NLS1242] - Anti-CCR1 antibody IHC of human lung. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/CCR1-Antibody-Immunohistochemistry-Paraffin-NLS1242-img0005.jpg "Immunohistochemistry-Paraffin: CCR1 Antibody [NLS1242] - Anti-CCR1 antibody IHC of human lung. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.")
![Immunohistochemistry-Paraffin: CCR1 Antibody [NLS1242] - Analysis of anti-CCR1 antibody with human spleen, lymphocytes.](http://images.novusbio.com/fullsize/CCR1-Antibody-Immunohistochemistry-Paraffin-NLS1242-img0001.jpg)
![Immunohistochemistry-Paraffin: CCR1 Antibody [NLS1242] - Analysis of anti-CCR1 antibody with human colon, carcinoma.](http://images.novusbio.com/fullsize/CCR1-Antibody-Immunohistochemistry-Paraffin-NLS1242-img0003.jpg)
![Immunohistochemistry-Paraffin: CCR1 Antibody [NLS1242] - Anti-CCR1 antibody IHC of human Lung, Adenocarcinoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/CCR1-Antibody-Immunohistochemistry-Paraffin-NLS1242-img0004.jpg)
![Immunohistochemistry: Adenosine A1R Antibody (JE31-35) [NBP3-32002] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Adenosine A1R antibody (NBP3-32002) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32002) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32002_rabbit-adenosine-a1r-mab-je31-35-298202413585567.jpg "Immunohistochemistry: Adenosine A1R Antibody (JE31-35) [NBP3-32002] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Adenosine A1R antibody (NBP3-32002) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32002) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.")
![Western Blot: Adenosine A1R Antibody (JE31-35) [NBP3-32002] - Western blot analysis of Adenosine A1R on different lysates with Rabbit anti-Adenosine A1R antibody (NBP3-32002) at 1/1,000 dilution. Lane 1: A549 cell lysate (15 ug/Lane) Lane 2: HEK-293 cell lysate (15 ug/Lane) Lane 3: U-87 MG cell lysate (15 ug/Lane) Lane 4: SH-SY5Y cell lysate (15 ug/Lane) Lane 5: HeLa cell lysate (15 ug/Lane) Lane 6: Raji cell lysate (15 ug/Lane) Lane 7: NIH/3T3 cell lysate (15 ug/Lane) Lane 8: Human brain tissue lysate (30 ug/Lane) Lane 9: Mouse brain tissue lysate (30 ug/Lane) Lane 10: Rat brain tissue lysate (30 ug/Lane) Lane 11: Human cerebellum tissue lysate (30 ug/Lane) Lane 12: Rat cerebellum tissue lysate (30 ug/Lane) Predicted band size: 36.5 kDa Observed band size: 36.5/40 kDa Exposure time: 5 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 (NBP3-32002) 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/nbp3-32002_rabbit-adenosine-a1r-mab-je31-35-392024845353.jpg)
![Western Blot: SP110 Antibody (PSH03-66) [NBP3-32973] - Western blot analysis of SP110 on different lysates with Rabbit anti-SP110 antibody (NBP3-32973) at 1/1,000 dilution. Lane 1: Jurkat cell lysate Lane 2: HeLa cell lysate Lane 3: HL-60 cell lysate Lane 4: SW480 cell lysate Lane 5: Daudi cell lysate Lane 6: K-562 cell lysate Lane 7: PC-3M cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 78 kDa Observed band size: 29-78 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 (NBP3-32973) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32973_rabbit-sp110-mab-psh03-66-288202412493449.jpg "Western Blot: SP110 Antibody (PSH03-66) [NBP3-32973] - Western blot analysis of SP110 on different lysates with Rabbit anti-SP110 antibody (NBP3-32973) at 1/1,000 dilution. Lane 1: Jurkat cell lysate Lane 2: HeLa cell lysate Lane 3: HL-60 cell lysate Lane 4: SW480 cell lysate Lane 5: Daudi cell lysate Lane 6: K-562 cell lysate Lane 7: PC-3M cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 78 kDa Observed band size: 29-78 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 (NBP3-32973) at 1/1,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: SP110 Antibody (PSH03-66) [NBP3-32973] - Immunohistochemical analysis of paraffin-embedded human lymph node tissue with Rabbit anti-SP110 antibody (NBP3-32973) at 1/2,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32973) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32973_rabbit-sp110-mab-psh03-66-29820241433360.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)
![Immunohistochemistry-Paraffin: Bradykinin RB1/BDKRB1 Antibody [NLS3580] - Human Vascular Smooth Muscle: Formalin-Fixed, paraffin-Embedded (FFPE)](http://images.novusbio.com/fullsize/Bradykinin-RB1-BDKRB1-Antibody-Immunohistochemistry-Paraffin-NLS3580-img0004.jpg "Immunohistochemistry-Paraffin: Bradykinin RB1/BDKRB1 Antibody [NLS3580] - Human Vascular Smooth Muscle: Formalin-Fixed, paraffin-Embedded (FFPE)")
![Immunohistochemistry-Paraffin: Bradykinin RB1/BDKRB1 Antibody [NLS3580] - Analysis of anti-BDKRB1 antibody with nasal mucosa at 24 ug/ml.](http://images.novusbio.com/fullsize/Bradykinin-RB1-BDKRB1-Antibody-Immunohistochemistry-Paraffin-NLS3580-img0002.jpg)
![Immunohistochemistry-Paraffin: Bradykinin RB1/BDKRB1 Antibody [NLS3580] - Analysis of anti-BDKRB1 antibody with human placenta.](http://images.novusbio.com/fullsize/Bradykinin-RB1-BDKRB1-Antibody-Immunohistochemistry-Paraffin-NLS3580-img0003.jpg)
![Immunohistochemistry-Paraffin: CXCR5 Antibody [NLS1385] - Human Small Intestine, B-Cell, Burkitt Lymphoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/CXCR5-Antibody-Immunohistochemistry-Paraffin-NLS1385-img0004.jpg "Immunohistochemistry-Paraffin: CXCR5 Antibody [NLS1385] - Human Small Intestine, B-Cell, Burkitt Lymphoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.")
![Immunohistochemistry-Paraffin: CXCR5 Antibody [NLS1385] - Analysis of anti-CXCR5 antibody with human spleen at 5 ug/ml.](http://images.novusbio.com/fullsize/CXCR5-Antibody-Immunohistochemistry-Paraffin-NLS1385-img0001.jpg)
![Immunohistochemistry-Paraffin: CXCR5 Antibody [NLS1385] - Analysis of anti-CXCR5 antibody with human lymph node, B-cell, mantle cell lymphoma.](http://images.novusbio.com/fullsize/CXCR5-Antibody-Immunohistochemistry-Paraffin-NLS1385-img0002.jpg)
![Immunohistochemistry-Paraffin: CXCR5 Antibody [NLS1385] - Human Lymph Node, Hodgkins Lymphoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/CXCR5-Antibody-Immunohistochemistry-Paraffin-NLS1385-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)
![Immunohistochemistry: Fc gamma RIII (CD16) Antibody (PD00-12) [NBP3-32127] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling Fc gamma RIII (CD16) with Rabbit anti-Fc gamma RIII (CD16) antibody (NBP3-32127) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32127, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32127_rabbit-fc-gamma-riii-cd16-mab-pd00-12-298202414333631.jpg "Immunohistochemistry: Fc gamma RIII (CD16) Antibody (PD00-12) [NBP3-32127] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling Fc gamma RIII (CD16) with Rabbit anti-Fc gamma RIII (CD16) antibody (NBP3-32127) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32127, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).")
![Immunohistochemistry: Fc gamma RIII (CD16) Antibody (PD00-12) [NBP3-32127] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-Fc gamma RIII (CD16) antibody (NBP3-32127) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32127) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32127_rabbit-fc-gamma-riii-cd16-mab-pd00-12-29820241435244.jpg)
![Immunocytochemistry/ Immunofluorescence: Fc gamma RIII (CD16) Antibody (PD00-12) [NBP3-32127] - Immunocytochemistry analysis of 293T cells labeling Fc gamma RIII (CD16) with Rabbit anti-Fc gamma RIII (CD16) antibody (NBP3-32127) at 1/100 dilution. Cells were fixed in 100% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Fc gamma RIII (CD16) antibody (NBP3-32127) at 1/100 dilution in 1% BSA in PBST 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. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32127_rabbit-fc-gamma-riii-cd16-mab-pd00-12-2920241192312.jpg)
![Flow Cytometry: Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) - Azide and BSA Free [NBP3-07899] - Separation of murine LPAM-1 positive cells (red-filled) from LPAM-1 negative cells (black-dashed) in flow cytometry analysis (surface staining) of murine splenocyte suspension stained using Rat Monoclonal Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) (concentration in sample 2 ug/ml) DAR APC.](http://images.novusbio.com/fullsize/Integrin-alpha-4-beta-7-LPAM-1-Antibody-DATK32-Azide-and-BSA-Free-Flow-Cytometry-NBP3-07899-img0002.jpg "Flow Cytometry: Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) - Azide and BSA Free [NBP3-07899] - Separation of murine LPAM-1 positive cells (red-filled) from LPAM-1 negative cells (black-dashed) in flow cytometry analysis (surface staining) of murine splenocyte suspension stained using Rat Monoclonal Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) (concentration in sample 2 ug/ml) DAR APC.")
![Flow Cytometry: Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) - Azide and BSA Free [NBP3-07899] - Flow cytometry surface staining pattern of murine splenocyte suspension stained usingRat Monoclonal Integrin alpha 4 beta 7/LPAM-1 Antibody (DATK32) (concentration in sample 2 ug/ml) DAR APC.](http://images.novusbio.com/fullsize/Integrin-alpha-4-beta-7-LPAM-1-Antibody-DATK32-Azide-and-BSA-Free-Flow-Cytometry-NBP3-07899-img0001.jpg)
![Immunohistochemistry: IKK alpha Antibody [NBP2-99049] - Immunochemical staining of human IKK in human colon carcinoma with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/IKK-alpha-Antibody-Immunohistochemistry-NBP2-99049-img0003.jpg "Immunohistochemistry: IKK alpha Antibody [NBP2-99049] - Immunochemical staining of human IKK in human colon carcinoma with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: IKK alpha Antibody [NBP2-99049] - Immunochemical staining of human IKK alpha in human breast carcinoma with rabbit polyclonal antibody at 1:300 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/IKK-alpha-Antibody-Immunohistochemistry-Paraffin-NBP2-99049-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: IKK alpha Antibody [NBP2-99049] - Immunofluorescence staining of IKK alpha in HCT116 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99049 antibody (dilution ratio 1:200) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus.](http://images.novusbio.com/fullsize/nbp2-99049_rabbit-polyclonal-ikk-alpha-antibody-2352025166478.png)
![Flow Cytometry: TRAIL R4/TNFRSF10D/DcR2 Antibody (TRAIL-R4-01) - Azide Free [NBP1-45027] - Staining of CD264-transfectants using anti-CD264 (TRAIL-R4-01) PE.](http://images.novusbio.com/fullsize/TRAIL-R4-TNFRSF10D-DcR2-Antibody-TRAIL-R4-01-Azide-Free-Flow-Cytometry-NBP1-45027-img0002.jpg "Flow Cytometry: TRAIL R4/TNFRSF10D/DcR2 Antibody (TRAIL-R4-01) - Azide Free [NBP1-45027] - Staining of CD264-transfectants using anti-CD264 (TRAIL-R4-01) PE.")
![Flow Cytometry: TRAIL R4/TNFRSF10D/DcR2 Antibody (TRAIL-R4-01) - Azide Free [NBP1-45027] - A surface stain was performed on HeLa cells with TRAIL R4/TNFRSF10D/DcR2 Antibody (TRAIL-R4-01) NBP1-45027PE and a matched isotype control (orange). Cells were incubated in an antibody dilution of 5 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to phycoerythrin.](http://images.novusbio.com/fullsize/TRAIL-R4-TNFRSF10D-DcR2-Antibody-TRAIL-R4-01-Azide-Free-Flow-Cytometry-NBP1-45027-img0001.jpg)
