| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-98877-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90488-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-98787-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-99593-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50171-0.025ml | |||
![Immunohistochemistry: Ki67/MKI67 Antibody (PSH0-02) [NBP3-32499] - Immunohistochemical analysis of paraffin-embedded human cervix carcinoma tissue with Rabbit anti-Ki67/MKI67 antibody (NBP3-32499) 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 (NBP3-32499) 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/nbp3-32499_rabbit-ki67-mki67-mab-psh0-02-298202414262672.jpg "Immunohistochemistry: Ki67/MKI67 Antibody (PSH0-02) [NBP3-32499] - Immunohistochemical analysis of paraffin-embedded human cervix carcinoma tissue with Rabbit anti-Ki67/MKI67 antibody (NBP3-32499) 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 (NBP3-32499) 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.")
![Flow Cytometry: Ki67/MKI67 Antibody (PSH0-02) [NBP3-32499] - Flow cytometric analysis of A431 cells labeling Ki67/MKI67. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32499, 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/nbp3-32499_rabbit-ki67-mki67-mab-psh0-02-29202416372190.jpg)
![Western Blot: Cyclin D3 Antibody [NBP2-98877] - Anti-Cyclin D3 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate. Lane B: Jurkat 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: 33 kDa](http://images.novusbio.com/fullsize/Cyclin-D3-Antibody-Western-Blot-NBP2-98877-img0002.jpg "Western Blot: Cyclin D3 Antibody [NBP2-98877] - Anti-Cyclin D3 rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate. Lane B: Jurkat 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: 33 kDa")
![Immunocytochemistry/Immunofluorescence: Cyclin D3 Antibody [NBP2-98877] - Immunofluorescence staining of Cyclin D3 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 NBP2-98877 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 and cytoplasm.](http://images.novusbio.com/fullsize/nbp2-98877_rabbit-polyclonal-cyclin-d3-antibody-23520251125446.png)
![Western Blot: ELF3/ESE-1 Antibody (JE33-30) [NBP3-32320] - Western blot analysis of ELF3/ESE-1 on different lysates with Rabbit anti-ELF3/ESE-1 antibody (NBP3-32320) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: SK-Br-3 cell lysate (10 ug/Lane) Lane 3: A431 cell lysate (10 ug/Lane) Lane 4: Mouse lung tissue lysate (20 ug/Lane) Lane 5: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 41.5 kDa Observed band size: 41.5 kDa Exposure time: 40 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 (NBP3-32320) 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/nbp3-32320_rabbit-elf3-ese-1-mab-je33-30-278202415212488.jpg "Western Blot: ELF3/ESE-1 Antibody (JE33-30) [NBP3-32320] - Western blot analysis of ELF3/ESE-1 on different lysates with Rabbit anti-ELF3/ESE-1 antibody (NBP3-32320) at 1/1,000 dilution. Lane 1: A549 cell lysate (10 ug/Lane) Lane 2: SK-Br-3 cell lysate (10 ug/Lane) Lane 3: A431 cell lysate (10 ug/Lane) Lane 4: Mouse lung tissue lysate (20 ug/Lane) Lane 5: Rat kidney tissue lysate (20 ug/Lane) Predicted band size: 41.5 kDa Observed band size: 41.5 kDa Exposure time: 40 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 (NBP3-32320) 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.")
![Flow Cytometry: ELF3/ESE-1 Antibody (JE33-30) [NBP3-32320] - Flow cytometric analysis of A431 cells labeling ELF3/ESE-1. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32320, 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/nbp3-32320_rabbit-elf3-ese-1-mab-je33-30-392024884669.jpg)
![Western Blot: MyoD Antibody (JE60-47) [NBP3-32630] - Western blot analysis of MyoD on different lysates with Rabbit anti-MyoD antibody (NBP3-32630) at 1/1,000 dilution. Lane 1: RD cell lysate Lane 2: HEK-293 cell lysate (negative) Lane 3: HeLa cell lysate (negative) Lane 4: RD cell lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 35 kDa Observed band size: 45 kDa Exposure time: 10 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 (NBP3-32630) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 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/nbp3-32630_rabbit-myod-mab-je60-47-278202416285250.jpg "Western Blot: MyoD Antibody (JE60-47) [NBP3-32630] - Western blot analysis of MyoD on different lysates with Rabbit anti-MyoD antibody (NBP3-32630) at 1/1,000 dilution. Lane 1: RD cell lysate Lane 2: HEK-293 cell lysate (negative) Lane 3: HeLa cell lysate (negative) Lane 4: RD cell lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 35 kDa Observed band size: 45 kDa Exposure time: 10 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 (NBP3-32630) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: MyoD Antibody (JE60-47) [NBP3-32630] - Immunocytochemistry analysis of RD (positive) and HEK-293 (negative) labeling MyoD with Rabbit anti-MyoD antibody (NBP3-32630) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS 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-MyoD antibody (NBP3-32630) 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/nbp3-32630_rabbit-myod-mab-je60-47-2920241192395.jpg)
![Immunohistochemistry-Paraffin: S100A6 Antibody (016) [NBP2-90488] - Immunochemical staining of mouse S100A6 in mouse spleen with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/S100A6-Antibody-016-Immunohistochemistry-Paraffin-NBP2-90488-img0002.jpg "Immunohistochemistry-Paraffin: S100A6 Antibody (016) [NBP2-90488] - Immunochemical staining of mouse S100A6 in mouse spleen with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: S100A6 Antibody (016) [NBP2-90488] - Immunochemical staining of mouse S100A6 in mouse kidney with rabbit monoclonal antibody (1:200, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/S100A6-Antibody-016-Immunohistochemistry-Paraffin-NBP2-90488-img0001.jpg)
![Western Blot: E2F-4 Antibody [NBP2-98787] - Lane A: K562 Whole Cell LysateLane B: Raji Whole Cell LysateLane C: HeLa Whole Cell LysateLane D: Jurkat Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:44 kDaObserved band size:53 kDa](http://images.novusbio.com/fullsize/E2F-4-Antibody-Western-Blot-NBP2-98787-img0002.jpg "Western Blot: E2F-4 Antibody [NBP2-98787] - Lane A: K562 Whole Cell LysateLane B: Raji Whole Cell LysateLane C: HeLa Whole Cell LysateLane D: Jurkat Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:44 kDaObserved band size:53 kDa")
![Immunocytochemistry/Immunofluorescence: E2F-4 Antibody [NBP2-98787] - Immunofluorescence staining of E2F-4 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 NBP2-98787 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/nbp2-98787_rabbit-polyclonal-e2f-4-antibody-235202511444414.png)
![Western Blot: IFRD1 Antibody [NBP2-99593] - Anti-IFRD1 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate Lane B: HeLa Whole Cell Lysate Lane C: MOLT4 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: 50 kDa. Observed band size: 50 kDa](http://images.novusbio.com/fullsize/IFRD1-Antibody-Western-Blot-NBP2-99593-img0003.jpg "Western Blot: IFRD1 Antibody [NBP2-99593] - Anti-IFRD1 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate Lane B: HeLa Whole Cell Lysate Lane C: MOLT4 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: 50 kDa. Observed band size: 50 kDa")
![Immunocytochemistry/Immunofluorescence: IFRD1 Antibody [NBP2-99593] - Immunofluorescence staining of IFRD1 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 NBP2-99593 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 .](http://images.novusbio.com/fullsize/nbp2-99593_rabbit-polyclonal-ifrd1-antibody-235202521525033.png)
![Western Blot: Cyclin G Antibody [NBP2-86608] - WB Suggested Anti-CCNG1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: MCF7 cell lysate](http://images.novusbio.com/fullsize/Cyclin-G-Antibody-Western-Blot-NBP2-86608-img0002.jpg "Western Blot: Cyclin G Antibody [NBP2-86608] - WB Suggested Anti-CCNG1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: MCF7 cell lysate")
![Immunohistochemistry-Paraffin: Cyclin G Antibody [NBP2-86608] - Rabbit Anti-CCNG1 Antibody. Formalin Fixed Paraffin Embedded Tissue: Human heart Tissue. Observed Staining: Nucleus. Primary Antibody Concentration: 1:100. Other Working Concentrations: N/A. Secondary Antibody: Donkey anti](http://images.novusbio.com/fullsize/Cyclin-G-Antibody-Immunohistochemistry-Paraffin-NBP2-86608-img0001.jpg)
![Western Blot: HGFR/c-MET Antibody (A9A4-R) [NBP3-32198] - Western blot analysis of HGFR/c-MET on different lysates with Mouse anti-HGFR/c-MET antibody (NBP3-32198) at 1/500 dilution. Lane 1: A549 cell lysate Lane 2: HepG2 cell lysate Lane 3: HT-29 cell lysate Lane 4: Hela cell lysate Lane 5: LO2 cell lysate Lane 6: SK-Br-3 cell lysate (Negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 156 kDa Observed band size: 145 kDa Exposure time: 1 minute; 6% 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 (NBP3-32198) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:150,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32198_mouse-hgfr-c-met-mab-a9a4-r-278202416331273.jpg "Western Blot: HGFR/c-MET Antibody (A9A4-R) [NBP3-32198] - Western blot analysis of HGFR/c-MET on different lysates with Mouse anti-HGFR/c-MET antibody (NBP3-32198) at 1/500 dilution. Lane 1: A549 cell lysate Lane 2: HepG2 cell lysate Lane 3: HT-29 cell lysate Lane 4: Hela cell lysate Lane 5: LO2 cell lysate Lane 6: SK-Br-3 cell lysate (Negative) Lysates/proteins at 30 ug/Lane. Predicted band size: 156 kDa Observed band size: 145 kDa Exposure time: 1 minute; 6% 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 (NBP3-32198) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:150,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: HGFR/c-MET Antibody (A9A4-R) [NBP3-32198] - Immunohistochemical analysis of paraffin-embedded human lung adenocarcinoma tissue with Mouse anti-HGFR/c-MET antibody (NBP3-32198) at 1/400 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 (NBP3-32198) at 1/400 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/nbp3-32198_mouse-hgfr-c-met-mab-a9a4-r-29820241416182.jpg)
![Immunoprecipitation: HGF R/c-MET Antibody (17) [NBP2-50171] - Immunoprecipitation of SNU-5 cell lysates using anti-c-Met [17]. Detection was performed by antibodies SC-10 and AF276.](http://images.novusbio.com/fullsize/HGF-R-c-MET-Antibody-17-Immunoprecipitation-NBP2-50171-img0001.jpg "Immunoprecipitation: HGF R/c-MET Antibody (17) [NBP2-50171] - Immunoprecipitation of SNU-5 cell lysates using anti-c-Met [17]. Detection was performed by antibodies SC-10 and AF276.")