| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54325-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26492-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26155-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54450-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26612-50ul | |||
![Immunohistochemistry-Paraffin: ACTH Antibody (SPM501) - C-terminus [NBP2-53160] - Formalin-fixed, paraffin-embedded Human Pituitary stained with ACTH Monoclonal Antibody (SPM501).](http://images.novusbio.com/fullsize/ACTH-Antibody-SPM501-C-terminus-Immunohistochemistry-Paraffin-NBP2-53160-img0001.jpg "Immunohistochemistry-Paraffin: ACTH Antibody (SPM501) - C-terminus [NBP2-53160] - Formalin-fixed, paraffin-embedded Human Pituitary stained with ACTH Monoclonal Antibody (SPM501).")
![Western Blot: FDFT1 Antibody (10H12) [NBP3-15199] - Positive WB detected in: THP-1 whole cell lysate, K562 whole cell lysate. All lanes: FDFT1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49, 41, 39, 36, 44 KDa. Observed band size: 50 KDa.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Western-Blot-NBP3-15199-img0003.jpg "Western Blot: FDFT1 Antibody (10H12) [NBP3-15199] - Positive WB detected in: THP-1 whole cell lysate, K562 whole cell lysate. All lanes: FDFT1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 49, 41, 39, 36, 44 KDa. Observed band size: 50 KDa.")
![Immunohistochemistry: FDFT1 Antibody (10H12) [NBP3-15199] - IHC image of FDFT1 antibody diluted at 1:100 and staining in paraffin-embedded human lung cancer. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Immunohistochemistry-NBP3-15199-img0002.jpg)
![Immunohistochemistry: FDFT1 Antibody (10H12) [NBP3-15199] - IHC image of FDFT1 antibody diluted at 1:100 and staining in paraffin-embedded human testis tissue. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/FDFT1-Antibody-10H12-Immunohistochemistry-NBP3-15199-img0001.jpg)
![Immunohistochemistry: SERCA2 ATPase Antibody (20D1) [NBP3-26492] - Image of SERCA2 ATPase Antibody (20D1) diluted at 1:50 and staining in paraffin-embedded human heart 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 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.41% DAB.](http://images.novusbio.com/fullsize/nbp3-26492_rabbit-serca2-atpase-mab-20d1-2722024820398.jpg "Immunohistochemistry: SERCA2 ATPase Antibody (20D1) [NBP3-26492] - Image of SERCA2 ATPase Antibody (20D1) diluted at 1:50 and staining in paraffin-embedded human heart 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 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.41% DAB.")
![Immunocytochemistry/Immunofluorescence: SERCA2 ATPase Antibody (20D1) [NBP3-26492] - Staining of MCF7 with SERCA2 ATPase Antibody (20D1) at 1:25, 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 509-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26492_rabbit-serca2-atpase-mab-20d1-28220241247516.jpg)
![Flow Cytometry: SERCA2 ATPase Antibody (20D1) [NBP3-26492] - Overlay Peak curve showing Hela cells stained with SERCA2 ATPase Antibody (20D1) (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/nbp3-26492_rabbit-serca2-atpase-mab-20d1-282202414312788.jpg)
![LINGO1 antibody [C1C3] detects LINGO1 protein by immunofluorescent analysis.Sample: DIV9 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: LINGO1 stained by LINGO1 antibody [C1C3] (NBP2-19359) diluted at 1:500.Red: beta Tubulin 3/ Tuj1, stained by beta Tubulin 3/ Tuj1 antibody [GT1338] diluted at 1:500.Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp2-19359_rabbit-polyclonal-lingo-1-antibody-immunocytochemistry-immunofluorescence-2611202518482321.jpg "LINGO1 antibody [C1C3] detects LINGO1 protein by immunofluorescent analysis.Sample: DIV9 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: LINGO1 stained by LINGO1 antibody [C1C3] (NBP2-19359) diluted at 1:500.Red: beta Tubulin 3/ Tuj1, stained by beta Tubulin 3/ Tuj1 antibody [GT1338] diluted at 1:500.Blue: Fluoroshield with DAPI .")
![Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with LINGO1 antibody [C1C3] (NBP2-19359) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-19359_rabbit-polyclonal-lingo-1-antibody-western-blot-2611202518191322.jpg)
![Immunohistochemistry-Paraffin: IRS2 Antibody [NB100-68244] - Human ovarian carcinoma. Antibody used at a dilution of 1:1,000.](http://images.novusbio.com/fullsize/IRS2-Antibody-Immunohistochemistry-Paraffin-NB100-68244-img0002.jpg "Immunohistochemistry-Paraffin: IRS2 Antibody [NB100-68244] - Human ovarian carcinoma. Antibody used at a dilution of 1:1,000.")
![<b>Independent Antibodies Validation. </b>Immunoprecipitation: IRS2 Antibody [NB100-68244] - Detection of Human IRS2 by Western Blot of Immunoprecipitates. Samples: Whole cell lysate (1 mg for IP, 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-IRS2 antibody NB100-68244 used for IP at 3 mcg/mg lysate. IRS2 was also immunoprecipitated by rabbit anti-IRS2 antibodies NB100-68242 and NB100-68243, which recognize upstream epitopes. Detection: Chemiluminescence with exposure times of 3 seconds (A) and 10 seconds (B).](http://images.novusbio.com/fullsize/IRS2-Antibody-Immunoprecipitation-NB100-68244-img0003.jpg)
![Western Blot: TRPC3 Antibody [NBP2-32258] - Samples: Whole cell lysate (50 ug) prepared using NETN or RIPA buffer from HeLa, 293T, and Jurkat cells. Antibodies: Affinity purified rabbit anti-TRPC3 antibody NBP2-32258 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/TRPC3-Antibody-Western-Blot-NBP2-32258-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: TRPC3 Antibody [NBP2-32258] - Samples: Whole cell lysate (50 ug) prepared using NETN or RIPA buffer from HeLa, 293T, and Jurkat cells. Antibodies: Affinity purified rabbit anti-TRPC3 antibody NBP2-32258 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![<b>Biological Strategies Validation. </b>Immunoprecipitation: TRPC3 Antibody [NBP2-32258] - Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) prepared using NETN buffer from 293T cells. Antibodies: Affinity purified rabbit anti-TRPC3 antibody NBP2-32258 used for IP at 6 ug per reaction. TRPC3 was also immunoprecipitated by rabbit anti-TRPC3 antibody BL16089. For blotting immunoprecipitated TRPC3, NBP2-32258 was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/TRPC3-Antibody-Immunoprecipitation-NBP2-32258-img0002.jpg)
![Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-262202414471525.jpg "Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Image of Monoamine Oxidase B Antibody (9B6) diluted at 1:100 and staining in paraffin-embedded human liver 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-26220241522417.jpg)
![Western Blot: Monoamine Oxidase B Antibody (9B6) [NBP3-26155] - Positive Western Blot detected in: L02 whole cell lysate, HepG2 whole cell lysate. All lanes: Monoamine Oxidase B Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 59, 47 kDa Observed band size: 59 kDa](http://images.novusbio.com/fullsize/nbp3-26155_rabbit-monoamine-oxidase-b-mab-9b6-282202411485834.jpg)
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Uterus stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0003.jpg "Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Uterus stained with ASRGL1 Monoclonal Antibody (CRASH/1289).")
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Fallopian Tube stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0001.jpg)
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Endometrium stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0002.jpg)
![Immunohistochemistry: CRMP2 Antibody (20D8) [NBP3-26612] - Image of CRMP2 Antibody (20D8) diluted at 1:50 and staining in paraffin-embedded human breast cancer 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 0.35% DAB.](http://images.novusbio.com/fullsize/nbp3-26612_rabbit-crmp2-mab-20d8-262202414471542.jpg "Immunohistochemistry: CRMP2 Antibody (20D8) [NBP3-26612] - Image of CRMP2 Antibody (20D8) diluted at 1:50 and staining in paraffin-embedded human breast cancer 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 0.35% DAB.")
![Immunocytochemistry/Immunofluorescence: CRMP2 Antibody (20D8) [NBP3-26612] - Staining of SH-SY5Y with CRMP2 Antibody (20D8) at 1:25, 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 506-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26612_rabbit-crmp2-mab-20d8-282202412493633.jpg)
![Flow Cytometry: CRMP2 Antibody (20D8) [NBP3-26612] - Overlay Peak curve showing SH-SY5Y cells stained with CRMP2 Antibody (20D8) (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/nbp3-26612_rabbit-crmp2-mab-20d8-282202414183684.jpg)
![Western Blot: OTP Antibody [NBP2-19642] - Sample (30 ug of whole cell lysate) A: NT2D1 12% SDS PAGE gel, diluted at 1:500.](http://images.novusbio.com/fullsize/OTP-Antibody-Western-Blot-NBP2-19642-img0001.jpg "Western Blot: OTP Antibody [NBP2-19642] - Sample (30 ug of whole cell lysate) A: NT2D1 12% SDS PAGE gel, diluted at 1:500.")
![Immunohistochemistry-Paraffin: OTP Antibody [NBP2-19642] - Sample: Paraffin-embedded mouse hind brain. OTP antibody dilution: 1:500.](http://images.novusbio.com/fullsize/OTP-Antibody-Immunohistochemistry-Paraffin-NBP2-19642-img0002.jpg)