| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99524-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90404-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90685-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90585-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98729-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89590-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90060-50ul | |||
![Western Blot: FAT10 Antibody [NBP2-99524] - Anti-FAT10 rabbit polyclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 25 kDa](http://images.novusbio.com/fullsize/FAT10-Antibody-Western-Blot-NBP2-99524-img0003.jpg "Western Blot: FAT10 Antibody [NBP2-99524] - Anti-FAT10 rabbit polyclonal antibody at 1:500 dilution. Lane A: HepG2 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 25 kDa")
![Immunocytochemistry/Immunofluorescence: FAT10 Antibody [NBP2-99524] - Immunofluorescence staining of FAT10 in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99524 antibody (dilution ratio 1:1000) 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/nbp2-99524_rabbit-polyclonal-fat10-antibody-23520251628192.png)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse spleen with rabbit monoclonal antibody (1:200). Positive staining was localized to Kupffer cell.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0003.jpg "Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse spleen with rabbit monoclonal antibody (1:200). Positive staining was localized to Kupffer cell.")
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse brain with rabbit monoclonal antibody (1:200). Positive staining was localized to microglia.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0001.jpg)
![Immunohistochemistry-Paraffin: Fc gamma RI/CD64 Antibody (008) [NBP2-90404] - Staining of mouse Fc gamma RI/CD64 in mouse liver with rabbit monoclonal antibody (1:100). Positive staining was localized to Kupffer cell.](http://images.novusbio.com/fullsize/Fc-gamma-RI-CD64-Antibody-008-Immunohistochemistry-Paraffin-NBP2-90404-img0002.jpg)
![Flow Cytometry: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] - Flow cytometric analysis of Mouse IFNGR1(CD119) expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse IFNGR1(CD119), then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/IFN-gamma-R1-CD119-Antibody-062-Flow-Cytometry-NBP2-90685-img0002.jpg "Flow Cytometry: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] - Flow cytometric analysis of Mouse IFNGR1(CD119) expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse IFNGR1(CD119), then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![Immunocytochemistry/ Immunofluorescence: IFN-gamma R1/CD119 Antibody (062) [NBP2-90685] -staining of mouse IFN-gamma R1/CD119 in mouse splenocytes. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90685 (1:60) at 4C overnight. Then cells were stained with the Alexa Fluor 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp2-90685_rabbit-monoclonal-ifn-gamma-r1-cd119-antibody-062-235202521451779.png)
![Western Blot: LAIR1 Antibody (PSH04-50) [NBP3-32517] - Western blot analysis of LAIR1 on different lysates with Mouse anti-LAIR1 antibody (NBP3-32517) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HL-60 cell lysate Lane 3: HeLa cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 32 kDa Observed band size: 40-45 kDa Exposure time: 30 seconds; ECL; 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 (NBP3-32517) at 1/2,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32517_mouse-lair1-mab-psh04-50-278202415242678.jpg "Western Blot: LAIR1 Antibody (PSH04-50) [NBP3-32517] - Western blot analysis of LAIR1 on different lysates with Mouse anti-LAIR1 antibody (NBP3-32517) at 1/2,000 dilution. Lane 1: THP-1 cell lysate Lane 2: HL-60 cell lysate Lane 3: HeLa cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 32 kDa Observed band size: 40-45 kDa Exposure time: 30 seconds; ECL; 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 (NBP3-32517) at 1/2,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: LAIR1 Antibody (PSH04-50) [NBP3-32517] - Immunohistochemical analysis of paraffin-embedded human lymph node tissue with Mouse anti-LAIR1 antibody (NBP3-32517) 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 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32517) at 1/200 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/nbp3-32517_mouse-lair1-mab-psh04-50-29820241492641.jpg)
![Flow Cytometry: ICAM-1/CD54 Antibody (009) [NBP2-90585] - Flow cytometric analysis of Mouse ICAM-1/CD54 expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse ICAM-1/CD54, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/ICAM-1-CD54-Antibody-009-Flow-Cytometry-NBP2-90585-img0001.jpg "Flow Cytometry: ICAM-1/CD54 Antibody (009) [NBP2-90585] - Flow cytometric analysis of Mouse ICAM-1/CD54 expression on BABL/c splenocytes. Cells were stained with purified anti-Mouse ICAM-1/CD54, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![Immunocytochemistry/Immunofluorescence: ICAM-1/CD54 Antibody (009) [NBP2-90585] - Immunofluorescence staining of Mouse ICAM-1/CD54 in Raw264.7 cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90585 antibody (dilution ratio 1:60) 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 Cytoplasm and Cell membrane.](http://images.novusbio.com/fullsize/nbp2-90585_rabbit-monoclonal-icam-1-cd54-antibody-009-23520252135170.png)
![Western Blot: CD48/SLAMF2 Antibody (JE37-98) [NBP3-32157] - Western blot analysis of CD48/SLAMF2 on different lysates with Rabbit anti-CD48/SLAMF2 antibody (NBP3-32157) at 1/1,000 dilution. Lane 1: Raji cell lysate Lane 2: Jurkat cell lysate Lysates/proteins at 15 ug/Lane. Predicted band size: 27.7 kDa Observed band size: 40 kDa Exposure time: 80 seconds; 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 (NBP3-32157) 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/nbp3-32157_rabbit-cd48-slamf2-mab-je37-98-2782024163160.jpg "Western Blot: CD48/SLAMF2 Antibody (JE37-98) [NBP3-32157] - Western blot analysis of CD48/SLAMF2 on different lysates with Rabbit anti-CD48/SLAMF2 antibody (NBP3-32157) at 1/1,000 dilution. Lane 1: Raji cell lysate Lane 2: Jurkat cell lysate Lysates/proteins at 15 ug/Lane. Predicted band size: 27.7 kDa Observed band size: 40 kDa Exposure time: 80 seconds; 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 (NBP3-32157) 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.")
![Immunohistochemistry: CD48/SLAMF2 Antibody (JE37-98) [NBP3-32157] - Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-CD48/SLAMF2 antibody (NBP3-32157) 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 (NBP3-32157) 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/nbp3-32157_rabbit-cd48-slamf2-mab-je37-98-29820241435245.jpg)
![Immunohistochemistry-Paraffin: IRF6 Antibody [NBP2-98729] - Staining of mouse IRF6 in mouse small intestine with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/IRF6-Antibody-Immunohistochemistry-Paraffin-NBP2-98729-img0002.jpg "Immunohistochemistry-Paraffin: IRF6 Antibody [NBP2-98729] - Staining of mouse IRF6 in mouse small intestine with rabbit polyclonal antibody (1:1000).")
![Immunocytochemistry/Immunofluorescence: IRF6 Antibody [NBP2-98729] - Immunofluorescence staining of IRF6 in COS7 cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98729 antibody (1:1000) 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 cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98729_rabbit-polyclonal-irf6-antibody-235202521451760.png)
![Western Blot: CD133 Antibody (A8C3-R) [NBP3-32124] - Western blot analysis of CD133 on different lysates with Mouse anti-CD133 antibody (NBP3-32124) at 1/5,000 dilution. Lane 1: HT-29 cell lysate Lane 2: SW480 cell lysate Lane 3: NCCIT cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 97 kDa Observed band size: 120 kDa Exposure time: 2 minutes; 10% 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 (NBP3-32124) at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32124_mouse-cd133-mab-a8c3-r-27820241631670.jpg "Western Blot: CD133 Antibody (A8C3-R) [NBP3-32124] - Western blot analysis of CD133 on different lysates with Mouse anti-CD133 antibody (NBP3-32124) at 1/5,000 dilution. Lane 1: HT-29 cell lysate Lane 2: SW480 cell lysate Lane 3: NCCIT cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 97 kDa Observed band size: 120 kDa Exposure time: 2 minutes; 10% 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 (NBP3-32124) at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD133 Antibody (A8C3-R) [NBP3-32124] - Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue with Mouse anti-CD133 antibody (NBP3-32124) 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 (NBP3-32124) 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/nbp3-32124_mouse-cd133-mab-a8c3-r-298202414161867.jpg)
![Immunohistochemistry-Paraffin: CX3CL1/Fractalkine Antibody (409) [NBP2-89590] - Staining of human CX3CL1 in human kidney with rabbit monoclonal antibody (1:100).](http://images.novusbio.com/fullsize/CX3CL1-Fractalkine-Antibody-409-Immunohistochemistry-Paraffin-NBP2-89590-img0002.jpg "Immunohistochemistry-Paraffin: CX3CL1/Fractalkine Antibody (409) [NBP2-89590] - Staining of human CX3CL1 in human kidney with rabbit monoclonal antibody (1:100).")
![Immunohistochemistry-Paraffin: CX3CL1/Fractalkine Antibody (409) [NBP2-89590] - Staining of human CX3CL1 in human pancreas with rabbit monoclonal antibody (1:100).](http://images.novusbio.com/fullsize/CX3CL1-Fractalkine-Antibody-409-Immunohistochemistry-Paraffin-NBP2-89590-img0001.jpg)
![Immunohistochemistry-Paraffin: ULBP-2 Antibody (022) [NBP2-90060] - Staining of human ULBP2 in human renal carcinoma with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/ULBP-2-Antibody-022-Immunohistochemistry-Paraffin-NBP2-90060-img0003.jpg "Immunohistochemistry-Paraffin: ULBP-2 Antibody (022) [NBP2-90060] - Staining of human ULBP2 in human renal carcinoma with rabbit monoclonal antibody (1:200).")
![Immunohistochemistry-Paraffin: ULBP-2 Antibody (022) [NBP2-90060] - Staining of human ULBP2 in human gastric cancer with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/ULBP-2-Antibody-022-Immunohistochemistry-Paraffin-NBP2-90060-img0004.jpg)
![Immunohistochemistry-Paraffin: ULBP-2 Antibody (022) [NBP2-90060] - Staining of human ULBP2 in human hepatoma with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/ULBP-2-Antibody-022-Immunohistochemistry-Paraffin-NBP2-90060-img0002.jpg)
![Flow Cytometry: Nectin-2/CD112 Antibody (R2.525) [NBP3-09163] - Separation of human CD112 positive thrombocytes(red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using anti-human CD112 (R2.525) purified antibody (concentration in sample 9 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/Nectin-2-CD112-Antibody-R2-525-Flow-Cytometry-NBP3-09163-img0002.jpg "Flow Cytometry: Nectin-2/CD112 Antibody (R2.525) [NBP3-09163] - Separation of human CD112 positive thrombocytes(red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using anti-human CD112 (R2.525) purified antibody (concentration in sample 9 ug/ml) GAM APC.")
![Flow Cytometry: Nectin-2/CD112 Antibody (R2.525) [NBP3-09163] - surface staining pattern of human peripheral whole blood stained using anti-human CD112 (R2.525) purified antibody (concentration in sample 9 ug/ml) GAM APC](http://images.novusbio.com/fullsize/Nectin-2-CD112-Antibody-R2-525-Flow-Cytometry-NBP3-09163-img0001.jpg)
![Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Separation of human neutrophil granulocytes (red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (intracellular staining) of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-MPO421-8B2-Flow-Intracellular-NBP2-41406-img0002.jpg "Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Separation of human neutrophil granulocytes (red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (intracellular staining) of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).")
![Flow (Intracellular): Myeloperoxidase/MPO Antibody (MPO421-8B2) [NBP2-41406] - Intracellular staining pattern of human peripheral whole blood stained using anti-human Myeloperoxidase (MPO421-8B2) purified antibody (concentration in sample 1 ug/ml).](http://images.novusbio.com/fullsize/Myeloperoxidase-MPO-Antibody-MPO421-8B2-Flow-Intracellular-NBP2-41406-img0001.jpg)