| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-03477-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-04201-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-37734-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26314-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21849-50ul | |||
![Western Blot: Protein Kinase A Regulatory Subunit II alpha Antibody [NBP3-03477] - Analysis of extracts from normal (control) and PRKAR2A knockout (KO) HeLa cells, using Protein Kinase A Regulatory Subunit II alpha antibody 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.](http://images.novusbio.com/fullsize/Protein-Kinase-A-Regulatory-Subunit-II-alpha-Antibody-Western-Blot-NBP3-03477-img0002.jpg "<b>Genetic Strategies Validation. </b>Western Blot: Protein Kinase A Regulatory Subunit II alpha Antibody [NBP3-03477] - Analysis of extracts from normal (control) and PRKAR2A knockout (KO) HeLa cells, using Protein Kinase A Regulatory Subunit II alpha antibody 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.")
![<b>Genetic Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Protein Kinase A Regulatory Subunit II alpha Antibody [NBP3-03477] - Analysis of L929 cells using [KO Validated] PRKAR2A Rabbit pAb at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining. Protein Kinase A Regulatory Subunit II alpha antibody](http://images.novusbio.com/fullsize/Protein-Kinase-A-Regulatory-Subunit-II-alpha-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-03477-img0001.jpg)
![Western Blot: Protein Kinase A Regulatory Subunit II alpha Antibody [NBP3-03477] - Analysis of extracts of various cell lines, using Protein Kinase A Regulatory Subunit II alpha antibody 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.](http://images.novusbio.com/fullsize/Protein-Kinase-A-Regulatory-Subunit-II-alpha-Antibody-Western-Blot-NBP3-03477-img0003.jpg)
![Western Blot: Synapsin II Antibody (7J6L0) [NBP3-15765] - Western blot analysis of extracts of 293T cells, using Synapsin II Rabbit mAb (NBP3-15765) 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: 90s.](http://images.novusbio.com/fullsize/Synapsin-II-Antibody-7J6L0-Western-Blot-NBP3-15765-img0001.jpg "Western Blot: Synapsin II Antibody (7J6L0) [NBP3-15765] - Western blot analysis of extracts of 293T cells, using Synapsin II Rabbit mAb (NBP3-15765) 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: 90s.")
![Immunocytochemistry/ Immunofluorescence: Synapsin II Antibody (7J6L0) [Synapsin II] - Confocal imaging of paraffin-embedded Mouse brain using Synapsin II Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). Objective: 40x. Perform microwave antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining.](http://images.novusbio.com/fullsize/nbp3-15765_rabbit-synapsin-ii-mab-7j6l0-52202517344258.jpg)
![Immunocytochemistry/ Immunofluorescence: Synapsin II Antibody (7J6L0) [Synapsin II] - Confocal imaging of paraffin-embedded Rat brain using Synapsin II Rabbit mAb followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) . DAPI was used for nuclear staining (Blue). Objective: 40x. Perform microwave antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining.](http://images.novusbio.com/fullsize/nbp3-15765_rabbit-synapsin-ii-mab-7j6l0-5220251733593.jpg)
![Western Blot: PAK1 Antibody [NBP3-04201] - Analysis of extracts of mouse kidney, using PAK1 antibody at 1:700 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.](http://images.novusbio.com/fullsize/PAK1-Antibody-Western-Blot-NBP3-04201-img0003.jpg "Western Blot: PAK1 Antibody [NBP3-04201] - Analysis of extracts of mouse kidney, using PAK1 antibody at 1:700 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.")
![Immunohistochemistry-Paraffin: PAK1 Antibody [NBP3-04201] - Paraffin-embedded human lung cancer using PAK1 antibody at dilution of 1:100 (40x lens).](http://images.novusbio.com/fullsize/PAK1-Antibody-Immunohistochemistry-Paraffin-NBP3-04201-img0002.jpg)
![Immunohistochemistry-Paraffin: PAK1 Antibody [NBP3-04201] - Paraffin-embedded rat spleen using PAK1 antibody at dilution of 1:100 (40x lens).](http://images.novusbio.com/fullsize/PAK1-Antibody-Immunohistochemistry-Paraffin-NBP3-04201-img0001.jpg)
![Western Blot: MAP2 Antibody (5B7) [NBP2-37734] - Western blot analysis using MAP2 mAb against human MAP2 recombinant protein. (Observed MW is 36.1 kDa)](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-Western-Blot-NBP2-37734-img0002.jpg "Western Blot: MAP2 Antibody (5B7) [NBP2-37734] - Western blot analysis using MAP2 mAb against human MAP2 recombinant protein. (Observed MW is 36.1 kDa)")
![Flow Cytometry: MAP2 Antibody (5B7) [NBP2-37734] - Flow cytometric analysis of HeLa cells using MAP2 Antibody (5B7) (green) and negative control (red).](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-Flow-Cytometry-NBP2-37734-img0003.jpg)
![ELISA: MAP2 Antibody (5B7) [NBP2-37734] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/MAP2-Antibody-5B7-ELISA-NBP2-37734-img0001.jpg)
![Western Blot: CRMP4 Antibody [NBP2-87213] - WB Suggested Anti-DPYSL3 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Transfected 293T](http://images.novusbio.com/fullsize/CRMP4-Antibody-Western-Blot-NBP2-87213-img0003.jpg "Western Blot: CRMP4 Antibody [NBP2-87213] - WB Suggested Anti-DPYSL3 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Transfected 293T")
![Immunohistochemistry: CRMP4 Antibody [NBP2-87213] - Immunohistochemistry with Small intestine, submucosal plexus tissue. Antibody concentration: 10ug/ml](http://images.novusbio.com/fullsize/CRMP4-Antibody-Immunohistochemistry-NBP2-87213-img0001.jpg)
![Immunoprecipitation: CRMP4 Antibody [NBP2-87213] - DRYSL3 was immunoprecipitated from 1 mg HEK293 Whole Cell Lysate with NBP2-87213 with 1:200 dilution. Western blot was performed using NBP2-87213 at 1/1000 dilution. Lane 1: Control IP in HEK293 Whole Cell Lysate. Lane 2: DRYSL3 IP with NBP2-87213](http://images.novusbio.com/fullsize/CRMP4-Antibody-Immunoprecipitation-NBP2-87213-img0004.jpg)
![Flow Cytometry: HDAC6 Antibody (159) [NBP3-09113] - Separation of K562 cells stained using anti-HDAC6 (159) purified antibody (concentration in sample 4,0 ug/ml, GAM APC, red-filled) from K562 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).](http://images.novusbio.com/fullsize/HDAC6-Antibody-159-Flow-Cytometry-NBP3-09113-img0001.jpg "Flow Cytometry: HDAC6 Antibody (159) [NBP3-09113] - Separation of K562 cells stained using anti-HDAC6 (159) purified antibody (concentration in sample 4,0 ug/ml, GAM APC, red-filled) from K562 cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).")
![Western Blot: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32811) at 1/1,000 dilution. Lane 1: Human brain tissue lysate Lane 2: Rat brain tissue lysate Lysates/proteins at 50 ug/Lane. Predicted band size: 46 kDa Observed band size: 35-100 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 (NBP3-32811) 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/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-288202412461627.jpg "Western Blot: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Western blot analysis of Tau on different lysates with Rabbit anti-Tau antibody (NBP3-32811) at 1/1,000 dilution. Lane 1: Human brain tissue lysate Lane 2: Rat brain tissue lysate Lysates/proteins at 50 ug/Lane. Predicted band size: 46 kDa Observed band size: 35-100 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 (NBP3-32811) 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: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Immunofluorescence analysis of paraffin-embedded mouse hippocampus tissue labeling Tau with Rabbit anti-Tau antibody (NBP3-32811) 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 (NBP3-32811, 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/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-29820241492636.jpg)
![Immunohistochemistry: Tau [p Thr231] Antibody (PSH01-04) [NBP3-32811] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Tau antibody (NBP3-32811) 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 (NBP3-32811) 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/nbp3-32811_rabbit-tau-p-thr231-mab-psh01-04-29820241420935.jpg)
![Immunohistochemistry: Brg1 Antibody (22F3) [NBP3-26314] - Image of Brg1 Antibody (22F3) diluted at 1:50 and staining in paraffin-embedded human stomach tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.44% DAB.](http://images.novusbio.com/fullsize/nbp3-26314_rabbit-brg1-mab-22f3-262202414471597.jpg "Immunohistochemistry: Brg1 Antibody (22F3) [NBP3-26314] - Image of Brg1 Antibody (22F3) diluted at 1:50 and staining in paraffin-embedded human stomach tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.44% DAB.")
![Immunohistochemistry: Brg1 Antibody (22F3) [NBP3-26314] - Image of Brg1 Antibody (22F3) diluted at 1:50 and staining in paraffin-embedded human stomach tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.44% DAB.](http://images.novusbio.com/fullsize/nbp3-26314_rabbit-brg1-mab-22f3-2722024831379.jpg)
![Immunocytochemistry/Immunofluorescence: Brg1 Antibody (22F3) [NBP3-26314] - Staining of Hela with Brg1 Antibody (22F3) at 1:20, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 511-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26314_rabbit-brg1-mab-22f3-2822024131225.jpg)
![Flow Cytometry: Brg1 Antibody (22F3) [NBP3-26314] - Overlay Peak curve showing Hela cells stained with Brg1 Antibody (22F3) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26314_rabbit-brg1-mab-22f3-282202414183640.jpg)
![Western Blot: PAK1 Antibody (SR2113) [NBP3-21849] - Western blot analysis using NBP3-21849 in A431 cell lysate.](http://images.novusbio.com/fullsize/nbp3-21849_rabbit-pak1-mab-sr2113-57202316582145.jpg "Western Blot: PAK1 Antibody (SR2113) [NBP3-21849] - Western blot analysis using NBP3-21849 in A431 cell lysate.")
![Immunohistochemistry: CLN3 Antibody - BSA Free [NBP3-47582] - Immunohistochemistry of paraffin-embedded human brain using (CLN3 antibody) at dilution of 1:50](http://images.novusbio.com/fullsize/nbp3-47582_rabbit-cln3-pab-bsa-free-284202511414829.jpg "Immunohistochemistry: CLN3 Antibody - BSA Free [NBP3-47582] - Immunohistochemistry of paraffin-embedded human brain using (CLN3 antibody) at dilution of 1:50")
![Western Blot: CLN3 Antibody - BSA Free [NBP3-47582] - SH-SY5Y cells were subjected to SDS PAGE followed by western blot with (CLN3 antibody) at dilution of 1:800](http://images.novusbio.com/fullsize/nbp3-47582_rabbit-cln3-pab-bsa-free-284202511352234.jpg)
![Western Blot: Inversin Antibody - BSA Free [NBP3-46466] - MCF7 cells were subjected to SDS PAGE followed by western blot with (Inversin antibody) at dilution of 1:100](http://images.novusbio.com/fullsize/nbp3-46466_rabbit-inversin-pab-bsa-free-28420251155440.jpg "Western Blot: Inversin Antibody - BSA Free [NBP3-46466] - MCF7 cells were subjected to SDS PAGE followed by western blot with (Inversin antibody) at dilution of 1:100")
![Immunohistochemistry: Inversin Antibody - BSA Free [NBP3-46466] - Immunohistochemistry of paraffin-embedded human breast cancer using (Inversin antibody) at dilution of 1:100](http://images.novusbio.com/fullsize/nbp3-46466_rabbit-inversin-pab-bsa-free-284202511553134.jpg)