| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-98482-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26410-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-29665-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26408-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26467-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26409-50ul | |||
![Immunocytochemistry/Immunofluorescence: SLK Antibody [NBP2-98482] - Immunofluorescence staining of SLK in A431 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98482 antibody (dilution ratio 1:200) at 4C overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm and cell membrane.](http://images.novusbio.com/fullsize/nbp2-98482_rabbit-polyclonal-slk-antibody-23520251664745.png "Immunocytochemistry/Immunofluorescence: SLK Antibody [NBP2-98482] - Immunofluorescence staining of SLK in A431 cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98482 antibody (dilution ratio 1:200) at 4C overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm and cell membrane.")
![Western Blot: BICD1 Antibody [NBP3-10679] - Western blot analysis of BICD1 in Human Thymus Tumor lysates. Antibody dilution at 1ug/ml](http://images.novusbio.com/fullsize/BICD1-Antibody-Western-Blot-NBP3-10679-img0001.jpg "Western Blot: BICD1 Antibody [NBP3-10679] - Western blot analysis of BICD1 in Human Thymus Tumor lysates. Antibody dilution at 1ug/ml")
![Immunohistochemistry: Tau [p Ser214] Antibody (31B12) [NBP3-26410] - Image of Tau [p Ser214] Antibody (31B12) diluted at 1:100 and staining in paraffin-embedded human brain 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 0.12% DAB.](http://images.novusbio.com/fullsize/nbp3-26410_rabbit-tau-p-ser-214-mab-31b12-26220241525333.jpg "Immunohistochemistry: Tau [p Ser214] Antibody (31B12) [NBP3-26410] - Image of Tau [p Ser214] Antibody (31B12) diluted at 1:100 and staining in paraffin-embedded human brain 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 0.12% DAB.")
![Western Blot: PAK1 [p Ser204] Antibody [NBP2-29665] - Untreated and pervanadate-treated NIH/3T3 cells (lanes 1 and 2, respectively) were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-PAK1 (Ser204) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated NIH/3T3 lysate was either unblocked, phosphorylated-peptide blocked, or non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-PAK1 (Ser204) (1:1,000). Lanes 4 and 5 were blocking peptides were the phosphorylated peptide used as the immunogen and the non-phopshrylated form of the peptide. Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated PAK1.](http://images.novusbio.com/fullsize/PAK1-[p-Ser204]-Antibody-Western-Blot-NBP2-29665-img0001.jpg "Western Blot: PAK1 [p Ser204] Antibody [NBP2-29665] - Untreated and pervanadate-treated NIH/3T3 cells (lanes 1 and 2, respectively) were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-PAK1 (Ser204) (1:1,000). Blocking Peptide Analysis: Pervanadate-treated NIH/3T3 lysate was either unblocked, phosphorylated-peptide blocked, or non-phosphorylated peptide blocked (lanes 3, 4, and 5, respectively) that are that were resolved by electrophoresis, transferred to PVDF and probed with anti-phospho-PAK1 (Ser204) (1:1,000). Lanes 4 and 5 were blocking peptides were the phosphorylated peptide used as the immunogen and the non-phopshrylated form of the peptide. Proteins were visualized using a goat anti-rabbit secondary antibody conjugated to HRP and a chemiluminescence detection system. Arrow indicates phosphorylated PAK1.")
![Immunohistochemistry: Tau [p Ser404] Antibody (11H10) [NBP3-26408] - Image of Tau [p Ser404] Antibody (11H10) diluted at 1:50 and staining in paraffin-embedded human brain 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 0.11% DAB.](http://images.novusbio.com/fullsize/nbp3-26408_rabbit-tau-p-ser-404-mab-11h10-2722024856318.jpg "Immunohistochemistry: Tau [p Ser404] Antibody (11H10) [NBP3-26408] - Image of Tau [p Ser404] Antibody (11H10) diluted at 1:50 and staining in paraffin-embedded human brain 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 0.11% DAB.")
![Western Blot: Calpain 2 Antibody (17E9) [NBP3-26467] - Positive Western Blot detected in: U87 whole cell lysate, U251 whole cell lysate, PC3 whole cell lysate, A549 whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate, MCF-7 whole cell lysate. All lanes: Calpain 2 Antibody at 1: 500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 80, 72 kDa Observed band size: 72-95 kDa](http://images.novusbio.com/fullsize/nbp3-26467_rabbit-calpain-2-mab-17e9-282202411485813.jpg "Western Blot: Calpain 2 Antibody (17E9) [NBP3-26467] - Positive Western Blot detected in: U87 whole cell lysate, U251 whole cell lysate, PC3 whole cell lysate, A549 whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate, MCF-7 whole cell lysate. All lanes: Calpain 2 Antibody at 1: 500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 80, 72 kDa Observed band size: 72-95 kDa")
![Immunohistochemistry-Paraffin: Tau Antibody (Tau46) [NBP2-42223] - Formalin fixed paraffin embedded human brain tissue stained with Tau antibody (NBP2-42223).](http://images.novusbio.com/fullsize/Tau-Antibody-Tau46-Immunohistochemistry-Paraffin-NBP2-42223-img0001.jpg "Immunohistochemistry-Paraffin: Tau Antibody (Tau46) [NBP2-42223] - Formalin fixed paraffin embedded human brain tissue stained with Tau antibody (NBP2-42223).")
![Immunocytochemistry/Immunofluorescence: Tau [p Ser324] Antibody (4E8) [NBP3-26409] - Staining of SH-SY5Y cells with Tau [p Ser324] Antibody (4E8) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26409_rabbit-tau-p-ser-324-mab-4e8-282202412493620.jpg "Immunocytochemistry/Immunofluorescence: Tau [p Ser324] Antibody (4E8) [NBP3-26409] - Staining of SH-SY5Y cells with Tau [p Ser324] Antibody (4E8) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).")