| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-88839-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-37302-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99488-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97449-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-21438-25ul | |||
![Western Blot: Antibody (AT2G10) [NBP2-88839] - The cell lysate (40ug) was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human Rac1,2,3 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.Lane 1. Jurkat cell lysate](http://images.novusbio.com/fullsize/Antibody-AT2G10-Western-Blot-NBP2-88839-img0002.jpg "Western Blot: Antibody (AT2G10) [NBP2-88839] - The cell lysate (40ug) was resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human Rac1,2,3 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.Lane 1. Jurkat cell lysate")
![Flow Cytometry: Antibody (AT2G10) [NBP2-88839] - Flow cytometry analysis of Rac1,2,3 in Jurkat cells. The cell was stained with at 2-5ug for 1x10^6cells (red). A Goat anti mouse IgG (Alexa fluor 488) was used as the secondary antibody. Mouse monoclonal IgG was used as the isotype control (dark gray), cells without incubation with primary and secondary antibody was used as the negative control (light gray).](http://images.novusbio.com/fullsize/Antibody-AT2G10-Flow-Cytometry-NBP2-88839-img0003.jpg)
![Western Blot: Antibody (AT2G10) [NBP2-88839] - The recombinant proteins (50ng) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human Rac1,2,3 antibody (1:1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.Lane 1.: Recombinant human Rac 1 proteinLane 2.: Recombinant human Rac 2 proteinLane 3.: Recombinant human Rac 3 protein](http://images.novusbio.com/fullsize/Antibody-AT2G10-Western-Blot-NBP2-88839-img0001.jpg)
![Western Blot: CPI17 alpha Antibody (4H10) [NBP1-04336] - The Cell lysates of A549 (30ug) were resolved by SDS-PAGE, transferred to NC membrane and probed with anti-human PPP1R14A (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.](http://images.novusbio.com/fullsize/CPI17-alpha-Antibody-4H10-Western-Blot-NBP1-04336-img0001.jpg "Western Blot: CPI17 alpha Antibody (4H10) [NBP1-04336] - The Cell lysates of A549 (30ug) were resolved by SDS-PAGE, transferred to NC membrane and probed with anti-human PPP1R14A (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.")
![Western Blot: CPI17 alpha Antibody (4H10) [NBP1-04336] - The Cell lysates (40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human PPP1R14A antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.Lane 1. : A549 cell lysate Lane 2. : NIH-3T3 cell lysate](http://images.novusbio.com/fullsize/CPI17-alpha-Antibody-4H10-Adhesion-Activation-NBP1-04336-img0002.jpg)
![Western Blot: MKK3/MKK6 Antibody (8R1J5) [NBP3-15946] - Western blot analysis of extracts of various cell lines, using MKK3/MKK6 Rabbit mAb (NBP3-15946) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.](http://images.novusbio.com/fullsize/MKK3-MKK6-Antibody-8R1J5-Western-Blot-NBP3-15946-img0001.jpg "Western Blot: MKK3/MKK6 Antibody (8R1J5) [NBP3-15946] - Western blot analysis of extracts of various cell lines, using MKK3/MKK6 Rabbit mAb (NBP3-15946) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.")
![Western Blot: MKK3/MKK6 Antibody (8R1J5) [NBP3-15946] - Western blot analysis of extracts of various cell lines, using MKK3/MKK6 Rabbit mAb (NBP3-15946) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 30s.](http://images.novusbio.com/fullsize/MKK3-MKK6-Antibody-8R1J5-Western-Blot-NBP3-15946-img0002.jpg)
![Western Blot: DARPP-32 Antibody (2A4G9) [NBP2-37302] - Western blot analysis using PPP1R1B mAb against HEK293 (1) and PPP1R1B (AA: 95-204)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/DARPP-32-Antibody-2A4G9-Western-Blot-NBP2-37302-img0003.jpg "Western Blot: DARPP-32 Antibody (2A4G9) [NBP2-37302] - Western blot analysis using PPP1R1B mAb against HEK293 (1) and PPP1R1B (AA: 95-204)-hIgGFc transfected HEK293 (2) cell lysate.")
![Western Blot: DARPP-32 Antibody (2A4G9) [NBP2-37302] - Western blot analysis using PPP1R1B mAb against human PPP1R1B (AA: 95-204) recombinant protein. (Expected MW is 38.3 kDa)](http://images.novusbio.com/fullsize/DARPP-32-Antibody-2A4G9-Western-Blot-NBP2-37302-img0002.jpg)
![ELISA: DARPP-32 Antibody (2A4G9) [NBP2-37302] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/DARPP-32-Antibody-2A4G9-ELISA-NBP2-37302-img0001.jpg)
![Flow Cytometry: DEP-1/CD148 Antibody (MEM-CD148/05) [NBP2-21790] - Surface staining of human peripheral blood leukocytes using anti-CD148 (MEM-CD148/05) PE.](http://images.novusbio.com/fullsize/DEP-1-CD148-Antibody-MEM-CD148-05-Flow-Cytometry-NBP2-21790-img0003.jpg "Flow Cytometry: DEP-1/CD148 Antibody (MEM-CD148/05) [NBP2-21790] - Surface staining of human peripheral blood leukocytes using anti-CD148 (MEM-CD148/05) PE.")
![Flow Cytometry: DEP-1/CD148 Antibody (MEM-CD148/05) [NBP2-21790] - Surface staining of human peripheral blood using anti-CD148 (MEM-CD148/05) APC.](http://images.novusbio.com/fullsize/DEP-1-CD148-Antibody-MEM-CD148-05-Flow-Cytometry-NBP2-21790-img0001.jpg)
![Flow Cytometry: DEP-1/CD148 Antibody (MEM-CD148/05) [NBP2-21790] - Surface staining of human peripheral blood leukocytes using anti-CD148 (MEM-CD148/05) biotin.](http://images.novusbio.com/fullsize/DEP-1-CD148-Antibody-MEM-CD148-05-Flow-Cytometry-NBP2-21790-img0002.jpg)
![Western Blot: Protein Phosphatase 1C gamma Antibody [NBP2-99488] - Anti-Protein Phosphatase 1C gamma rabbit polyclonal antibody at 1:500 dilution. Lane A: 293T Whole Cell Lysate Lane B: HepG2 Whole Cell Lysate Lane C: HeLa 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: 37 kDa. Observed band size: 37 kDa](http://images.novusbio.com/fullsize/Protein-Phosphatase-1C-gamma-Antibody-Western-Blot-NBP2-99488-img0003.jpg "Western Blot: Protein Phosphatase 1C gamma Antibody [NBP2-99488] - Anti-Protein Phosphatase 1C gamma rabbit polyclonal antibody at 1:500 dilution. Lane A: 293T Whole Cell Lysate Lane B: HepG2 Whole Cell Lysate Lane C: HeLa 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: 37 kDa. Observed band size: 37 kDa")
![Immunocytochemistry/Immunofluorescence: Protein Phosphatase 1C gamma Antibody [NBP2-99488] - Immunofluorescence staining of Protein Phosphatase 1C gamma 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 NBP2-99488 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) and counterstained with DAPI (blue).Positive staining was localized to Nucleus .](http://images.novusbio.com/fullsize/nbp2-99488_rabbit-polyclonal-protein-phosphatase-1c-gamma-antibody-235202514492337.png)
![Immunohistochemistry-Paraffin: PPP2R1B Antibody [NBP2-97449] - Immunochemical staining of human PPP2R1B in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/PPP2R1B-Antibody-Immunohistochemistry-Paraffin-NBP2-97449-img0002.jpg "Immunohistochemistry-Paraffin: PPP2R1B Antibody [NBP2-97449] - Immunochemical staining of human PPP2R1B in human testis with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunocytochemistry/Immunofluorescence: PPP2R1B Antibody [NBP2-97449] - Immunofluorescence staining of PPP2R1B 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 NBP2-97449 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/nbp2-97449_rabbit-polyclonal-ppp2r1b-antibody-23520251664710.png)
![Western Blot: Kv10.2 Antibody [NBP2-83132] - WB Suggested Anti-KCNH5 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:312500. Positive Control: HepG2 cell lysate](http://images.novusbio.com/fullsize/Kv10.2-Antibody-Western-Blot-NBP2-83132-img0002.jpg "Western Blot: Kv10.2 Antibody [NBP2-83132] - WB Suggested Anti-KCNH5 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:312500. Positive Control: HepG2 cell lysate")
![Immunohistochemistry: Kv10.2 Antibody [NBP2-83132] - Human Brain](http://images.novusbio.com/fullsize/Kv10.2-Antibody-Immunohistochemistry-NBP2-83132-img0001.jpg)
![Western Blot: ATAD2 Antibody (JE34-52) [NBP3-32052] - Western blot analysis of ATAD2 on different lysates with Rabbit anti-ATAD2 antibody (NBP3-32052) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: MCF7 cell lysate Lane 3: T-47D cell lysate Lane 4: HT-29 cell lysate Lane 5: Saos- 2 cell lysate Lane 6: HepG2 cell lysate Lane 7: Jurkat cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 158 kDa Observed band size: 180 kDa Exposure time: 4 minutes 41 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 (NBP3-32052) 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/nbp3-32052_rabbit-atad2-mab-je34-52-278202415295524.jpg "Western Blot: ATAD2 Antibody (JE34-52) [NBP3-32052] - Western blot analysis of ATAD2 on different lysates with Rabbit anti-ATAD2 antibody (NBP3-32052) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: MCF7 cell lysate Lane 3: T-47D cell lysate Lane 4: HT-29 cell lysate Lane 5: Saos- 2 cell lysate Lane 6: HepG2 cell lysate Lane 7: Jurkat cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 158 kDa Observed band size: 180 kDa Exposure time: 4 minutes 41 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 (NBP3-32052) 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: ATAD2 Antibody (JE34-52) [NBP3-32052] - Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-ATAD2 antibody (NBP3-32052) 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 (NBP3-32052) 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/nbp3-32052_rabbit-atad2-mab-je34-52-298202414333676.jpg)
![Immunocytochemistry/ Immunofluorescence: DUSP23 Antibody [NBP3-21438] - Immunofluorescence staining of DUSP23 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP3-21438 (dilution ratio 1:100) 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). Positive staining was localized to Nucleus and Cytoplasm.](http://images.novusbio.com/fullsize/nbp3-21438_rabbit-dusp23-pab-23520251664746.png)
![Immunohistochemistry: LMW-PTP/ACP1 Antibody (PSH04-57) [NBP3-31992] - Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-LMW-PTP/ACP1 antibody (NBP3-31992) 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 (NBP3-31992) 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/nbp3-31992_rabbit-lmw-ptp-acp1-mab-psh04-57-298202414333658.jpg "Immunohistochemistry: LMW-PTP/ACP1 Antibody (PSH04-57) [NBP3-31992] - Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-LMW-PTP/ACP1 antibody (NBP3-31992) 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 (NBP3-31992) 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: LMW-PTP/ACP1 Antibody (PSH04-57) [NBP3-31992] - Western blot analysis of LMW-PTP/ACP1 on different lysates with Rabbit anti-LMW-PTP/ACP1 antibody (NBP3-31992) at 1/2,000 dilution. Lane 1: HepG2 cell lysate Lane 2: HeLa cell lysate Lane 3: Jurkat cell lysate Lane 4: COS-1 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 18 kDa Observed band size: 18 kDa Exposure time: 1 minute 33 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 (NBP3-31992) at 1/2,000 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/nbp3-31992_rabbit-lmw-ptp-acp1-mab-psh04-57-3920248453523.jpg)
![Immunocytochemistry/ Immunofluorescence: PTEN [p Ser380] Antibody (JJ08-81) [NBP3-32791] - ICC staining of PTEN in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP3-32791, 1/100) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32791_rabbit-pten-p-ser380-mab-jj08-81-2920241192374.jpg "Immunocytochemistry/ Immunofluorescence: PTEN [p Ser380] Antibody (JJ08-81) [NBP3-32791] - ICC staining of PTEN in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (NBP3-32791, 1/100) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).")