| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26322-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-81571-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26116-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26521-50ul | |||
![Western Blot: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Positive Western Blot detected in: U251 whole cell lysate. All lanes: EAAT2/GLT1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 62 kDa Observed band size: 62 kDa](http://images.novusbio.com/fullsize/nbp3-26322_rabbit-eaat2-glt1-mab-28f9-28220241140946.jpg "Western Blot: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Positive Western Blot detected in: U251 whole cell lysate. All lanes: EAAT2/GLT1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 62 kDa Observed band size: 62 kDa")
![Flow Cytometry: EAAT2/GLT1 Antibody (28F9) [NBP3-26322] - Overlay Peak curve showing MCF-7 cells stained with EAAT2/GLT1 Antibody (28F9) (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/nbp3-26322_rabbit-eaat2-glt1-mab-28f9-282202414183678.jpg)
![Immunoprecipitation: NUMBL Antibody [NB100-88136] - Detection of Human NUMBL1 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-NUMBL1 antibody Nb100-88136 used for IP at 3 mcg/mg lysate. NUMBL1 was also immunoprecipitated by rabbit anti-NUMBL1 antibody NB100-88137, which recognizes a downstream epitope. Detection: Chemiluminescence with an exposure time of 3 seconds.](http://images.novusbio.com/fullsize/NUMBL-Antibody-Immunoprecipitation-NB100-88136-img0003.jpg "<b>Independent Antibodies Validation. </b>Immunoprecipitation: NUMBL Antibody [NB100-88136] - Detection of Human NUMBL1 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-NUMBL1 antibody Nb100-88136 used for IP at 3 mcg/mg lysate. NUMBL1 was also immunoprecipitated by rabbit anti-NUMBL1 antibody NB100-88137, which recognizes a downstream epitope. Detection: Chemiluminescence with an exposure time of 3 seconds.")
![Immunohistochemistry-Paraffin: KCNK10 Antibody [NBP1-81571] - Staining of human pancreas shows strong cytoplasmic positivity in exocrine glandular cells.](http://images.novusbio.com/fullsize/KCNK10-Antibody-Immunohistochemistry-Paraffin-NBP1-81571-img0002.jpg "Immunohistochemistry-Paraffin: KCNK10 Antibody [NBP1-81571] - Staining of human pancreas shows strong cytoplasmic positivity in exocrine glandular cells.")
![Western Blot: Stathmin-2/STMN2 Antibody [NBP3-42093] - Sample: Lane1: Porcine Cerebrum lysate; Lane2: Rat Cerebrum lysate Primary Ab: 0.1ug/ml NBP3-42093; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-42093_rabbit-stathmin-2-stmn2-pab-612202421373013.jpg "Western Blot: Stathmin-2/STMN2 Antibody [NBP3-42093] - Sample: Lane1: Porcine Cerebrum lysate; Lane2: Rat Cerebrum lysate Primary Ab: 0.1ug/ml NBP3-42093; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody")
![Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26116_rabbit-ndufs4-mab-9h1-27220248573312.jpg "Immunohistochemistry: Ndufs4 Antibody (9H1) [NBP3-26116] - Image of Ndufs4 Antibody (9H1) diluted at 1:100 and staining in paraffin-embedded human small intestine 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 0.05% DAB.")
![Flow Cytometry: Ndufs4 Antibody (9H1) [NBP3-26116] - Overlay Peak curve showing MCF7 cells stained with Ndufs4 Antibody (9H1) (red line) at 1:100. 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/nbp3-26116_rabbit-ndufs4-mab-9h1-282202414312761.jpg)
![Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253325.jpg "Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253314.jpg)