| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26552-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26159-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26650-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-22198-50ul | |||
![Western Blot: EPB42 Antibody [NBP3-41310] - Sample: Recombinant protein.](http://images.novusbio.com/fullsize/nbp3-41310_rabbit-epb42-pab-612202421283886.jpg "Western Blot: EPB42 Antibody [NBP3-41310] - Sample: Recombinant protein.")
![Western Blot: t-Plasminogen Activator/tPA Antibody (K12) [NBP3-41559] - Lane 1: Human Serum; Lane 2: Human Plasma; Lane 3: Porcine Serum; Lane 4: Rat Mammary gland lysate; Primary Ab: 4ug/ml NBP3-41559; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41559_mouse-t-plasminogen-activator-tpa-mab-k12-141202515123714.jpg "Western Blot: t-Plasminogen Activator/tPA Antibody (K12) [NBP3-41559] - Lane 1: Human Serum; Lane 2: Human Plasma; Lane 3: Porcine Serum; Lane 4: Rat Mammary gland lysate; Primary Ab: 4ug/ml NBP3-41559; Second Ab: 0.2ug/mL HRP-conjugated Goat Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: PDGF-BB Antibody (4#) [NBP3-41127] - Sample: Recombinant PDGFBB, Human.](http://images.novusbio.com/fullsize/nbp3-41127_mouse-pdgf-bb-mab-4-612202421304368.jpg "Western Blot: PDGF-BB Antibody (4#) [NBP3-41127] - Sample: Recombinant PDGFBB, Human.")
![Immunohistochemistry: alpha-Galactosidase A/GLA Antibody (30H11) [NBP3-26552] - Image of alpha-Galactosidase A/GLA Antibody (30H11) diluted at 1:100 and staining in paraffin-embedded human rectal 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 polymer IgG labeled by HRP and visualized using 0.14% DAB.](http://images.novusbio.com/fullsize/nbp3-26552_rabbit-alpha-galactosidase-a-gla-mab-30h11-26220241510617.jpg "Immunohistochemistry: alpha-Galactosidase A/GLA Antibody (30H11) [NBP3-26552] - Image of alpha-Galactosidase A/GLA Antibody (30H11) diluted at 1:100 and staining in paraffin-embedded human rectal 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 polymer IgG labeled by HRP and visualized using 0.14% DAB.")
![Flow Cytometry: alpha-Galactosidase A/GLA Antibody (30H11) [NBP3-26552] - Overlay Peak curve showing Hela cells stained with alpha-Galactosidase A/GLA Antibody (30H11) (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/nbp3-26552_rabbit-alpha-galactosidase-a-gla-mab-30h11-282202414312742.jpg)
![Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) 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 505-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241249369.jpg "Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) 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 505-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: LYVE-1 Antibody (11C11) [NBP3-26159] - Overlay Peak curve showing HepG2 cells stained with LYVE-1 Antibody (11C11) (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/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241418361.jpg)
![Western Blot: SRFBP1 Antibody [NBP1-52655] - Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Affinity purified rabbit anti-p49/STRAP antibody used for WB at 0.4 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. p49/STRAP was also immunoprecipitated by another rabbit anti-p49/STRAP antibody, which recognizes an upstream epitope.](http://images.novusbio.com/fullsize/SRFBP1-Antibody-Western-Blot-NBP1-52655-img0002.jpg "<b>Independent Antibodies Validation. </b>Western Blot: SRFBP1 Antibody [NBP1-52655] - Whole cell lysate (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) from HeLa cells. Affinity purified rabbit anti-p49/STRAP antibody used for WB at 0.4 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. p49/STRAP was also immunoprecipitated by another rabbit anti-p49/STRAP antibody, which recognizes an upstream epitope.")
![Western Blot: TBX3 Antibody [NBP1-71853] - Whole cell lysate from HeLa (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) and 293T (T; 50 mcg) cells. Affinity purified rabbit anti-TBX3 antibody used for WB at 0.4 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. TBX3 was also immunoprecipitated by another rabbit anti-TBX3 antibody which recognizes a downstream epitope.](http://images.novusbio.com/fullsize/TBX3-Antibody-Western-Blot-NBP1-71853-img0003.jpg "<b>Independent Antibodies Validation and Biological Strategies Validation.</b>Western Blot: TBX3 Antibody [NBP1-71853] - Whole cell lysate from HeLa (5, 15 and 50 mcg for WB; 1 mg for IP, 20% of IP loaded) and 293T (T; 50 mcg) cells. Affinity purified rabbit anti-TBX3 antibody used for WB at 0.4 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. TBX3 was also immunoprecipitated by another rabbit anti-TBX3 antibody which recognizes a downstream epitope.")
![Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) diluted at 1:100 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 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/nbp3-26650_rabbit-clusterin-apoj-mab-2a1-262202414471524.jpg "Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) diluted at 1:100 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 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Clusterin/APOJ Antibody (2A1) [NBP3-26650] - Image of Clusterin/APOJ Antibody (2A1) diluted at 1:100 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 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/nbp3-26650_rabbit-clusterin-apoj-mab-2a1-262202415475621.jpg)
![Western Blot: Apolipoprotein D Antibody (SR1458) [NBP3-22198] - Western blot analysis using NBP3-22198 in Human plasma lysate.](http://images.novusbio.com/fullsize/nbp3-22198_rabbit-apolipoprotein-d-mab-sr1458-57202317215159.jpg "Western Blot: Apolipoprotein D Antibody (SR1458) [NBP3-22198] - Western blot analysis using NBP3-22198 in Human plasma lysate.")