| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-49463-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26154-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26195-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26319-50ul | |||
![Immunoprecipitation: PTRF Antibody [NB100-60634] - Detection of Human PTRF 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-PTRF antibody NB100-60634 used for IP at 3 mcg/mg lysate. PTRF was also immunoprecipitated by rabbit anti-PTRF antibodies NB100-60633 and NB100-60635, which recognize other epitopes. Detection: Chemiluminescence with exposure times of 3 seconds (A and B).](http://images.novusbio.com/fullsize/PTRF-Antibody-Immunoprecipitation-NB100-60634-img0003.jpg "<b>Independent Antibodies Validation. </b>Immunoprecipitation: PTRF Antibody [NB100-60634] - Detection of Human PTRF 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-PTRF antibody NB100-60634 used for IP at 3 mcg/mg lysate. PTRF was also immunoprecipitated by rabbit anti-PTRF antibodies NB100-60633 and NB100-60635, which recognize other epitopes. Detection: Chemiluminescence with exposure times of 3 seconds (A and B).")
![Cynomolgus Monkey C-Peptide ELISA Kit (Colorimetric) [NBP2-59957] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp2-59957_cynomolgus-monkey-c-peptide-elisa-kit-colorimetric-312024831591.png "Cynomolgus Monkey C-Peptide ELISA Kit (Colorimetric) [NBP2-59957] - Standard Curve Reference")
![Immunohistochemistry-Paraffin: INPP5E Antibody [NBP2-49463] - Staining of human gallbladder shows moderate cytoplasmic positivity in glandular cells.](http://images.novusbio.com/fullsize/INPP5E-Antibody-Immunohistochemistry-Paraffin-NBP2-49463-img0004.jpg "Immunohistochemistry-Paraffin: INPP5E Antibody [NBP2-49463] - Staining of human gallbladder shows moderate cytoplasmic positivity in glandular cells.")
![Western Blot: LC3B Antibody (7D11) [NBP3-26154] - Positive Western Blot detected in: HepG2 whole cell lysate, U87 whole cell lysate, RAW264.7 whole cell lysate, U251 whole cell lysate, Hela whole cell lysate. All lanes: LC3B Antibody at 1: 500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 kDa Observed band size: 15 kDa](http://images.novusbio.com/fullsize/nbp3-26154_rabbit-lc3b-mab-7d11-28220241144268.jpg "Western Blot: LC3B Antibody (7D11) [NBP3-26154] - Positive Western Blot detected in: HepG2 whole cell lysate, U87 whole cell lysate, RAW264.7 whole cell lysate, U251 whole cell lysate, Hela whole cell lysate. All lanes: LC3B Antibody at 1: 500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 kDa Observed band size: 15 kDa")
![Flow Cytometry: LC3B Antibody (7D11) [NBP3-26154] - Overlay Peak curve showing Hela cells stained with LC3B Antibody (7D11) (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/nbp3-26154_rabbit-lc3b-mab-7d11-282202414183621.jpg)
![Immunohistochemistry: Insulin Antibody (1F6) [NBP3-26195] - Image of Insulin Antibody (1F6) diluted at 1:100 and staining in paraffin-embedded human pancreatic 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/nbp3-26195_rabbit-insulin-mab-1f6-262202414225223.jpg "Immunohistochemistry: Insulin Antibody (1F6) [NBP3-26195] - Image of Insulin Antibody (1F6) diluted at 1:100 and staining in paraffin-embedded human pancreatic 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: Insulin Antibody (1F6) [NBP3-26195] - Image of Insulin Antibody (1F6) diluted at 1:100 and staining in paraffin-embedded human pancreatic 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/nbp3-26195_rabbit-insulin-mab-1f6-26220241447152.jpg)
![Immunohistochemistry: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical 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/nbp3-26319_rabbit-glut1-mab-2e1-262202414471578.jpg "Immunohistochemistry: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical 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: Glut1 Antibody (2E1) [NBP3-26319] - Image of Glut1 Antibody (2E1) diluted at 1:100 and staining in paraffin-embedded human cervical 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/nbp3-26319_rabbit-glut1-mab-2e1-262202415355735.jpg)