| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11430 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47960-0.1mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26195-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11534 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26525-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26606-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11438 | |||
![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)
![Western Blot: ABP1/AOC1 Antibody (C12) [NBP3-41560] - 293T cell lysate Primary Ab: 3ug/ml NBP3-41560; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41560_mouse-abp1-aoc1-mab-c12-141202515123717.jpg "Western Blot: ABP1/AOC1 Antibody (C12) [NBP3-41560] - 293T cell lysate Primary Ab: 3ug/ml NBP3-41560; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody")
![Flow Cytometry: ABP1/AOC1 Antibody (C12) [NBP3-41560] - Human THP1 cell line was fixed with 2% paraformaldehyde (10 min), permeabilised with 0.1% BSA-Triton X-100, then stained with 10ug/ml NBP3-41560 (red histogram) or Isotype control antibody (green histogram), followed by 1ug/ml FITC-conjugated Anti-mouse IgG Secondary Antibody](http://images.novusbio.com/fullsize/nbp3-41560_mouse-abp1-aoc1-mab-c12-141202515123710.jpg)
![Flow Cytometry: Siglec-2/CD22 Antibody (MYG13) [NBP2-44602] - Flow Cytometric Analysis of Ramos cells using Siglec-2/CD22 Antibody (MYG13) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).](http://images.novusbio.com/fullsize/Siglec-2-CD22-Antibody-MYG13-Flow-Cytometry-NBP2-44602-img0002.jpg "Flow Cytometry: Siglec-2/CD22 Antibody (MYG13) [NBP2-44602] - Flow Cytometric Analysis of Ramos cells using Siglec-2/CD22 Antibody (MYG13) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red).")
![Western Blot: ACTR3 Antibody (7E5) [NBP3-26525] - Positive Western Blot detected in: PC-3 whole cell lysate, K562 whole cell lysate, HL-60 whole cell lysate, A549 whole cell lysate, Mouse Spleen whole cell lysate, Rat Spleen whole cell lysate. All lanes: Arp3 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 48 kDa Observed band size: 48 kDa](http://images.novusbio.com/fullsize/nbp3-26525_rabbit-actr3-mab-7e5-28220241147213.jpg "Western Blot: ACTR3 Antibody (7E5) [NBP3-26525] - Positive Western Blot detected in: PC-3 whole cell lysate, K562 whole cell lysate, HL-60 whole cell lysate, A549 whole cell lysate, Mouse Spleen whole cell lysate, Rat Spleen whole cell lysate. All lanes: Arp3 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 48 kDa Observed band size: 48 kDa")
![Immunohistochemistry: EGF Antibody (18B12) [NBP3-26606] - Image of EGF Antibody (18B12) diluted at 1:100 and staining in paraffin-embedded human skin 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 0.66% DAB.](http://images.novusbio.com/fullsize/nbp3-26606_rabbit-egf-mab-18b12-262202414225218.jpg "Immunohistochemistry: EGF Antibody (18B12) [NBP3-26606] - Image of EGF Antibody (18B12) diluted at 1:100 and staining in paraffin-embedded human skin 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 0.66% DAB.")
![Flow Cytometry: EGF Antibody (18B12) [NBP3-26606] - Overlay Peak curve showing SH-SY5Y cells stained with EGF Antibody (18B12) (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/nbp3-26606_rabbit-egf-mab-18b12-282202414183693.jpg)