| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-90227-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-34075-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-87531-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-48635-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47908-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-48364 | |||
![Immunohistochemistry-Paraffin: beta-2 Adrenergic R/ADRB2 Antibody [NBP1-90227] - Staining of human skeletal muscle shows very weak membranous positivity in myocytes.](http://images.novusbio.com/fullsize/beta-2-Adrenergic-R-ADRB2-Antibody-Immunohistochemistry-Paraffin-NBP1-90227-img0006.jpg "Immunohistochemistry-Paraffin: beta-2 Adrenergic R/ADRB2 Antibody [NBP1-90227] - Staining of human skeletal muscle shows very weak membranous positivity in myocytes.")
![CD11 Antibody [NBP3-14697] - : Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from MUTZ-3 cellsprepared using NETN lysis buffer. Antibodies: Rabbit antiCD11b recombinant monoclonal antibody used for IP at 20 ul/mg lysate. CD11bwas also immunoprecipitated by rabbit anti-CD11bantibody. For blotting immunoprecipitatedCD11b, was used at 1:1000.Chemiluminescence with an exposure time of 10 seconds.](http://images.novusbio.com/fullsize/CD11-Antibody-NBP3-14697-img0001.jpg "CD11 Antibody [NBP3-14697] - : Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from MUTZ-3 cellsprepared using NETN lysis buffer. Antibodies: Rabbit antiCD11b recombinant monoclonal antibody used for IP at 20 ul/mg lysate. CD11bwas also immunoprecipitated by rabbit anti-CD11bantibody. For blotting immunoprecipitatedCD11b, was used at 1:1000.Chemiluminescence with an exposure time of 10 seconds.")
![Immunocytochemistry/Immunofluorescence: Peptidylglycine alpha-Amidating Monooxygenase/PAM Antibody [NBP2-34075] - Staining of human cell line U-2 OS shows localization to cytosol. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/Peptidylglycine-alpha-Amidating-Monooxygenase-PAM-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-34075-img0004.jpg "Immunocytochemistry/Immunofluorescence: Peptidylglycine alpha-Amidating Monooxygenase/PAM Antibody [NBP2-34075] - Staining of human cell line U-2 OS shows localization to cytosol. Antibody staining is shown in green.")
![Immunohistochemistry-Paraffin: Peptidylglycine alpha-Amidating Monooxygenase/PAM Antibody [NBP2-34075] - Staining of human lymph node shows low expression as expected.](http://images.novusbio.com/fullsize/Peptidylglycine-alpha-Amidating-Monooxygenase-PAM-Antibody-Immunohistochemistry-Paraffin-NBP2-34075-img0010.jpg)
![Immunohistochemistry-Paraffin: GPR17 Antibody [NBP1-87531] - Staining in human cerebral cortex and liver tissues . Corresponding GPR17 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/GPR17-Antibody-Immunohistochemistry-Paraffin-NBP1-87531-img0007.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: GPR17 Antibody [NBP1-87531] - Staining in human cerebral cortex and liver tissues . Corresponding GPR17 RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: GPR17 Antibody [NBP1-87531] - Staining of human liver shows no positivity in hepatocytes as expected.](http://images.novusbio.com/fullsize/GPR17-Antibody-Immunohistochemistry-Paraffin-NBP1-87531-img0006.jpg)
![Immunohistochemistry-Paraffin: GPR17 Antibody [NBP1-87531] - Staining of human cerebellum shows moderate positivity in oligodendrocytes.](http://images.novusbio.com/fullsize/GPR17-Antibody-Immunohistochemistry-Paraffin-NBP1-87531-img0004.jpg)
![Immunohistochemistry-Paraffin: GPR17 Antibody [NBP1-87531] - Staining of human cerebral cortex shows moderate positivity in oligodendrocytes.](http://images.novusbio.com/fullsize/GPR17-Antibody-Immunohistochemistry-Paraffin-NBP1-87531-img0005.jpg)
![Immunohistochemistry-Paraffin: TRPM2 Antibody [NBP2-48635] - Staining of human lymph node shows high expression.](http://images.novusbio.com/fullsize/TRPM2-Antibody-Immunohistochemistry-Paraffin-NBP2-48635-img0003.jpg "Immunohistochemistry-Paraffin: TRPM2 Antibody [NBP2-48635] - Staining of human lymph node shows high expression.")
![Immunohistochemistry: TRPM2 Antibody [NBP2-48635] - Staining of human cerebellum shows strong cytoplasmic positivity in Purkinje cells.](http://images.novusbio.com/fullsize/TRPM2-Antibody-Immunohistochemistry-NBP2-48635-img0001.jpg)
![Immunohistochemistry-Paraffin: TRPM2 Antibody [NBP2-48635] - Staining of human kidney shows low expression as expected.](http://images.novusbio.com/fullsize/TRPM2-Antibody-Immunohistochemistry-Paraffin-NBP2-48635-img0002.jpg)
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: TRPM2 Antibody [NBP2-48635] - Staining in human lymph node and kidney tissues using anti-TRPM2 antibody. Corresponding TRPM2 RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/TRPM2-Antibody-Immunohistochemistry-Paraffin-NBP2-48635-img0004.jpg)
![Immunoprecipitation: CD38 Antibody [NBP3-14707] - Whole cell lysate (0.5 or 1.0mg per IP reaction; 20% of IP loaded) from 293T cellsprepared using NETN lysis buffer. Antibodies: Affinitypurified rabbit anti-CDC123 antibody used for IP at 6 ug per reaction. CDC123was also immunoprecipitated by rabbit anti-CDC123antibody BL19660. For blotting immunoprecipitatedCDC123, was used at 1 ug/ml. Detection:Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/CD38-Antibody-Immunoprecipitation-NBP3-14707-img0001.jpg "Immunoprecipitation: CD38 Antibody [NBP3-14707] - Whole cell lysate (0.5 or 1.0mg per IP reaction; 20% of IP loaded) from 293T cellsprepared using NETN lysis buffer. Antibodies: Affinitypurified rabbit anti-CDC123 antibody used for IP at 6 ug per reaction. CDC123was also immunoprecipitated by rabbit anti-CDC123antibody BL19660. For blotting immunoprecipitatedCDC123, was used at 1 ug/ml. Detection:Chemiluminescence with an exposure time of 30 seconds.")
![Immunocytochemistry/Immunofluorescence: Complement C3 Antibody (HL1643) - Azide and BSA Free [NBP3-25389] - C3 antibody [HL1643] detects C3 protein by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: C3 stained by C3 antibody [HL1643] (NBP3-25389) diluted at 1:500. Blue: Fluoroshield with DAPI .](http://images.novusbio.com/fullsize/nbp3-25389_rabbit-complement-c3-mab-hl1643-azide-and-bsa-free-2120249422664.jpg "Immunocytochemistry/Immunofluorescence: Complement C3 Antibody (HL1643) - Azide and BSA Free [NBP3-25389] - C3 antibody [HL1643] detects C3 protein by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: C3 stained by C3 antibody [HL1643] (NBP3-25389) diluted at 1:500. Blue: Fluoroshield with DAPI .")
![Western Blot: Complement C3 Antibody (HL1643) - Azide and BSA Free [NBP3-25389] - Human plasma (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with C3 antibody [HL1643] (NBP3-25389) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25389_rabbit-complement-c3-mab-hl1643-azide-and-bsa-free-2120249435517.jpg)
![Western Blot: Complement C3 Antibody (HL1643) - Azide and BSA Free [NBP3-25389] - Rat plasma (30 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with C3 antibody [HL1643] (NBP3-25389) diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25389_rabbit-complement-c3-mab-hl1643-azide-and-bsa-free-2120249362747.jpg)
![Western Blot: MEK5 Antibody [NBP1-97478] - Analysis of MEK5, pAb: Lane 1: Jurkat, Lane 2: Mouse Testes, Lane 3: Rat Brain](http://images.novusbio.com/fullsize/MEK5-Antibody-Western-Blot-NBP1-97478-img0001.jpg "Western Blot: MEK5 Antibody [NBP1-97478] - Analysis of MEK5, pAb: Lane 1: Jurkat, Lane 2: Mouse Testes, Lane 3: Rat Brain")
![Western Blot: VIPR1/VPAC1 Antibody (PD00-96) [NBP3-33097] - Western blot analysis of VIPR1/VPAC1 on different lysates with Rabbit anti-VIPR1/VPAC1 antibody (NBP3-33097) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: Jurkat cell lysate (20 ug/Lane) Lane 3: Raji cell lysate (20 ug/Lane) Lane 4: HT-29 cell lysate (20 ug/Lane) Lane 5: Caco-2 cell lysate (20 ug/Lane) Lane 6: MCF7 cell lysate (20 ug/Lane) Lane 7: MDA-MB-231 cell lysate (20 ug/Lane) Lane 8: PC-12 cell lysate (20 ug/Lane) Lane 9: LNCaP cell lysate (20 ug/Lane) Predicted band size: 52 kDa Observed band size: 55 kDa Exposure time: 2 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 (NBP3-33097) at 1/1,000 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/nbp3-33097_rabbit-vipr1-vpac1-mab-pd00-96-288202414191544.jpg "Western Blot: VIPR1/VPAC1 Antibody (PD00-96) [NBP3-33097] - Western blot analysis of VIPR1/VPAC1 on different lysates with Rabbit anti-VIPR1/VPAC1 antibody (NBP3-33097) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: Jurkat cell lysate (20 ug/Lane) Lane 3: Raji cell lysate (20 ug/Lane) Lane 4: HT-29 cell lysate (20 ug/Lane) Lane 5: Caco-2 cell lysate (20 ug/Lane) Lane 6: MCF7 cell lysate (20 ug/Lane) Lane 7: MDA-MB-231 cell lysate (20 ug/Lane) Lane 8: PC-12 cell lysate (20 ug/Lane) Lane 9: LNCaP cell lysate (20 ug/Lane) Predicted band size: 52 kDa Observed band size: 55 kDa Exposure time: 2 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 (NBP3-33097) at 1/1,000 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: VIPR1/VPAC1 Antibody (PD00-96) [NBP3-33097] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-VIPR1/VPAC1 antibody (NBP3-33097) at 1/4,000 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 (NBP3-33097) at 1/4,000 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/nbp3-33097_rabbit-vipr1-vpac1-mab-pd00-96-298202414304187.jpg)
![Sandwich ELISA: KAL1 Antibody (2E8) [H00003730-M01] - Detection limit for recombinant GST tagged KAL1 is approximately 1ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/KAL1-Antibody-2E8-Sandwich-ELISA-H00003730-M01-img0002.jpg "Sandwich ELISA: KAL1 Antibody (2E8) [H00003730-M01] - Detection limit for recombinant GST tagged KAL1 is approximately 1ng/ml as a capture antibody.")