| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97729-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89490-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90037-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98678-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89884-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89366-50ul | |||
![Flow Cytometry: CD52 Antibody (HI186) [NB500-311] - Flow cytometry analysis of CD52 in patients suffering with Acute Lymphoblastic Leukemia (anti-human CD52 (HI186); detection by Goat anti-mouse IgG2b PE). Fig. 1A CD52 positive cALL (gate leukemic cells).](http://images.novusbio.com/fullsize/CD52-Antibody-HI186-Flow-Cytometry-NB500-311-img0004.jpg "Flow Cytometry: CD52 Antibody (HI186) [NB500-311] - Flow cytometry analysis of CD52 in patients suffering with Acute Lymphoblastic Leukemia (anti-human CD52 (HI186); detection by Goat anti-mouse IgG2b PE). Fig. 1A CD52 positive cALL (gate leukemic cells).")
![Flow Cytometry: CD52 Antibody (HI186) [NB500-311] - Fig.1B CD52 negative pro T ALL (gate leukemic cells)](http://images.novusbio.com/fullsize/CD52-Antibody-HI186-Flow-Cytometry-NB500-311-img0003.jpg)
![Immunohistochemistry-Paraffin: FKBP6 Antibody [NBP2-97729] - Immunochemical staining of human FKBP6 in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/FKBP6-Antibody-Immunohistochemistry-Paraffin-NBP2-97729-img0002.jpg "Immunohistochemistry-Paraffin: FKBP6 Antibody [NBP2-97729] - Immunochemical staining of human FKBP6 in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunocytochemistry/Immunofluorescence: FKBP6 Antibody [NBP2-97729] - Immunofluorescence staining of FKBP6 in A431 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-97729 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) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm.](http://images.novusbio.com/fullsize/nbp2-97729_rabbit-polyclonal-fkbp6-antibody-23520251628187.png)
![Flow Cytometry: Granzyme A Antibody (CB9) [NBP3-14619] - Flow cytometry intracellular staining pattern of human peripheral whole blood stained using anti-human Granzyme A (CB9) purified antibody (concentration in sample 5,0 ug/ml, GAM APC).](http://images.novusbio.com/fullsize/Granzyme-A-Antibody-CB9-Flow-Cytometry-NBP3-14619-img0002.jpg "Flow Cytometry: Granzyme A Antibody (CB9) [NBP3-14619] - Flow cytometry intracellular staining pattern of human peripheral whole blood stained using anti-human Granzyme A (CB9) purified antibody (concentration in sample 5,0 ug/ml, GAM APC).")
![Flow Cytometry: Granzyme A Antibody (CB9) [NBP3-14619] - Separation of human Granzyme A positive NK cells (red-filled) from Granzyme A negative lymphocytes (black-dashed) in flow cytometry analysis (intracellular staining) of human peripheral whole blood stained using anti-human Granzyme A (CB9) purified antibody (concentration in sample 5,0 ug/ml, GAM APC).](http://images.novusbio.com/fullsize/Granzyme-A-Antibody-CB9-Flow-Cytometry-NBP3-14619-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: BMP-2 Antibody (110) [NBP2-89490] - Staining of Human BMP2 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human BMP2 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/BMP-2-Antibody-110-Immunocytochemistry-Immunofluorescence-NBP2-89490-img0001.jpg "Immunocytochemistry/Immunofluorescence: BMP-2 Antibody (110) [NBP2-89490] - Staining of Human BMP2 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human BMP2 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.")
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human breast cancer with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0003.jpg "Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human breast cancer with rabbit monoclonal antibody (1:300).")
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human melanoma with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0001.jpg)
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human skin with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0002.jpg)
![Western Blot: IL-12 p70/IL-12A Antibody [NBP2-98678] - Lane A: MOLT4 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:26 kDa Observed band size:38 kDa (We are unsure as to the identity of these extra bands.)](http://images.novusbio.com/fullsize/IL-12-p70-IL-12A-Antibody-Western-Blot-NBP2-98678-img0003.jpg "Western Blot: IL-12 p70/IL-12A Antibody [NBP2-98678] - Lane A: MOLT4 Whole Cell Lysate Lysates/proteins at 30 ug per lane.Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution.Developed using the Odyssey technique. Performed under reducing conditions.Predicted band size:26 kDa Observed band size:38 kDa (We are unsure as to the identity of these extra bands.)")
![Immunohistochemistry-Paraffin: IL-12 p70/IL-12A Antibody [NBP2-98678] - Human breast carcinoma with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/IL-12-p70-IL-12A-Antibody-Immunohistochemistry-Paraffin-NBP2-98678-img0002.jpg)
![Immunohistochemistry: CD47 Antibody (PD00-33) [NBP3-32156] - Immunohistochemical analysis of paraffin-embedded human ovarian tumor tissue with Rabbit anti-CD47 antibody (NBP3-32156) 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 (NBP3-32156) 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/nbp3-32156_rabbit-cd47-mab-pd00-33-298202414161868.jpg "Immunohistochemistry: CD47 Antibody (PD00-33) [NBP3-32156] - Immunohistochemical analysis of paraffin-embedded human ovarian tumor tissue with Rabbit anti-CD47 antibody (NBP3-32156) 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 (NBP3-32156) 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.")
![Flow Cytometry: CD47 Antibody (PD00-33) [NBP3-32156] - Flow cytometric analysis of Jurkat cells labeling CD47. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32156, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32156_rabbit-cd47-mab-pd00-33-392024884610.jpg)
![Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/Clusterin-APOJ-Antibody-013-Flow-Cytometry-NBP2-89884-img0002.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Clusterin/APOJ Antibody (013) [NBP2-89884] - Staining of Human CLU in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89884 antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-89884_rabbit-monoclonal-clusterin-apoj-antibody-013-235202514371330.png)
![Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 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 (NBP3-32196) at 1/2,000 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/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-27820241521244.jpg "Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 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 (NBP3-32196) at 1/2,000 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: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/8,000 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 (NBP3-32196) at 1/8,000 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/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-29820241492623.jpg)
![Immunohistochemistry-Paraffin: CD23/Fc epsilon RII Antibody (160) [NBP2-89366] - Staining of human CD23 in human lymph node with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/CD23-Fc-epsilon-RII-Antibody-160-Immunohistochemistry-Paraffin-NBP2-89366-img0003.jpg "Immunohistochemistry-Paraffin: CD23/Fc epsilon RII Antibody (160) [NBP2-89366] - Staining of human CD23 in human lymph node with rabbit monoclonal antibody (1:200).")
![Immunohistochemistry-Paraffin: CD23/Fc epsilon RII Antibody (160) [NBP2-89366] - Staining of human CD23 in human tonsil with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/CD23-Fc-epsilon-RII-Antibody-160-Immunohistochemistry-Paraffin-NBP2-89366-img0001.jpg)
![Immunohistochemistry-Paraffin: CD23/Fc epsilon RII Antibody (160) [NBP2-89366] - Staining of human CD23 in human spleen with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/CD23-Fc-epsilon-RII-Antibody-160-Immunohistochemistry-Paraffin-NBP2-89366-img0002.jpg)
![Immunohistochemistry: CD117/c-kit Antibody (PD00-24) [NBP3-32188] - Immunohistochemical analysis of paraffin-embedded human seminoma tissue with Rabbit anti-CD117/c-kit antibody (NBP3-32188) 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 (NBP3-32188) 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/nbp3-32188_rabbit-cd117-c-kit-mab-pd00-24-29820241435262.jpg "Immunohistochemistry: CD117/c-kit Antibody (PD00-24) [NBP3-32188] - Immunohistochemical analysis of paraffin-embedded human seminoma tissue with Rabbit anti-CD117/c-kit antibody (NBP3-32188) 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 (NBP3-32188) 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: LAG-3 Antibody (PSH0-42) [NBP3-32513] - Western blot analysis of LAG-3 on different lysates with Rabbit anti-LAG-3 antibody (NBP3-32513) at 1/2,000 dilution. Lane 1: NIH/3T3 transfected with LAG3 expression vector, whole cell lysate Lane 2: NIH/3T3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 57.4 kDa Observed band size: 55/70 kDa (Glycosylation) Exposure time: 1 minute 10 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 (NBP3-32513) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32513_rabbit-lag-3-mab-psh0-42-278202416285213.jpg "Western Blot: LAG-3 Antibody (PSH0-42) [NBP3-32513] - Western blot analysis of LAG-3 on different lysates with Rabbit anti-LAG-3 antibody (NBP3-32513) at 1/2,000 dilution. Lane 1: NIH/3T3 transfected with LAG3 expression vector, whole cell lysate Lane 2: NIH/3T3 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 57.4 kDa Observed band size: 55/70 kDa (Glycosylation) Exposure time: 1 minute 10 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 (NBP3-32513) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: LAG-3 Antibody (PSH0-42) [NBP3-32513] - Immunocytochemistry analysis of NIH/3T3 cells transfected with or without LAG3 labeling LAG-3 with Rabbit anti-LAG-3 antibody (NBP3-32513) at 1/100 dilution. Cells were fixed in 100% methanol for 10 minutes, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes, and then blocked with 1% BSA for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-LAG-3 antibody (NBP3-32513) at 1/100 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. 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/nbp3-32513_rabbit-lag-3-mab-psh0-42-2920241192322.jpg)