| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-84328-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26680-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | MAB79672-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26497-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21592-50ul | |||
![Western Blot: epithelial Sodium Channel beta Antibody [NBP3-18257] - Western blot analysis of Mouse mpkCCD cell lysates showing detection of epithelial Sodium Channel beta protein using Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257). Primary Antibody: Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257) at 1:1000.](http://images.novusbio.com/fullsize/epithelial-Sodium-Channel-beta-Antibody-Western-Blot-NBP3-18257-img0003.jpg "Western Blot: epithelial Sodium Channel beta Antibody [NBP3-18257] - Western blot analysis of Mouse mpkCCD cell lysates showing detection of epithelial Sodium Channel beta protein using Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257). Primary Antibody: Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257) at 1:1000.")
![Immunohistochemistry: epithelial Sodium Channel beta Antibody [NBP3-18257] - Immunohistochemistry analysis using Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257). Tissue: kidney tissue. Species: Rat. Primary Antibody: Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257) at 1:100. Secondary Antibody: FITC Goat Anti-Rabbit (green).](http://images.novusbio.com/fullsize/epithelial-Sodium-Channel-beta-Antibody-Immunohistochemistry-NBP3-18257-img0001.jpg)
![Western Blot: epithelial Sodium Channel beta Antibody [NBP3-18257] - Western blot analysis of Rat kidney tissue lysates showing detection of epithelial Sodium Channel beta protein using Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257). Primary Antibody: Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257) at 1:1000.](http://images.novusbio.com/fullsize/epithelial-Sodium-Channel-beta-Antibody-Western-Blot-NBP3-18257-img0002.jpg)
![Western Blot: epithelial Sodium Channel beta Antibody [NBP3-18257] - Western blot analysis of Mouse kidney cortex showing detection of epithelial Sodium Channel beta protein using Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257). Primary Antibody: Rabbit Anti-epithelial Sodium Channel beta Polyclonal Antibody (NBP3-18257) at 1:1000. Low-salt diet (lanes 1-4) compared to a high-salt diet (lanes 5-8).](http://images.novusbio.com/fullsize/epithelial Sodium Channel beta Antibody-Western Blot-NBP3-18257-img0004.jpg)
![Western Blot: WASP [p Ser483, p Ser484] Antibody [NB100-2307] - Detection of Human Phospho WASP (S483/S484) by Western Blot. Samples: Whole cell lysate (50 ug) from Jurkat and 293T cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-Phospho WASP (S483/S484) antibody NB100-2307 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/WASP-[p-Ser483--p-Ser484]-Antibody-Western-Blot-NB100-2307-img0006.jpg "<b>Biological Strategies Validation. </b>Western Blot: WASP [p Ser483, p Ser484] Antibody [NB100-2307] - Detection of Human Phospho WASP (S483/S484) by Western Blot. Samples: Whole cell lysate (50 ug) from Jurkat and 293T cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-Phospho WASP (S483/S484) antibody NB100-2307 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![Western Blot: Filamin A Antibody [NB100-58812] - Whole cell lysate (5, 15 and 50 ug for WB) from HeLa cells. Antibody used for WB at 0.04 ug/ml.](http://images.novusbio.com/fullsize/Filamin-A-Antibody-Western-Blot-NB100-58812-img0003.jpg "Western Blot: Filamin A Antibody [NB100-58812] - Whole cell lysate (5, 15 and 50 ug for WB) from HeLa cells. Antibody used for WB at 0.04 ug/ml.")
![Immunohistochemistry-Paraffin: Filamin A Antibody [NB100-58812] - Sample: FFPE section of human colon carcinoma. Antibody: Affinity purified rabbit anti-Filamin A used at a dilution of 1:1,000 (0.2ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/Filamin-A-Antibody-Immunohistochemistry-Paraffin-NB100-58812-img0005.jpg)
![Immunohistochemistry: CD44 Antibody (19H12) [NBP3-26680] - Image of CD44 Antibody (19H12) diluted at 1:50 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 0.51% DAB.](http://images.novusbio.com/fullsize/nbp3-26680_rabbit-cd44-mab-19h12-2622024152247.jpg "Immunohistochemistry: CD44 Antibody (19H12) [NBP3-26680] - Image of CD44 Antibody (19H12) diluted at 1:50 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 0.51% DAB.")
![Immunohistochemistry: CD44 Antibody (19H12) [NBP3-26680] - Image of CD44 Antibody (19H12) diluted at 1:50 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 0.51% DAB.](http://images.novusbio.com/fullsize/nbp3-26680_rabbit-cd44-mab-19h12-262202415253312.jpg)
![Western Blot: CD44 Antibody (19H12) [NBP3-26680] - Positive Western Blot detected in: A549 whole cell lysate, MCF7 whole cell lysate, HepG2 whole cell lysate.<br /> All lanes: CD44 Antibody at 1: 1000<br /> Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.<br /> Predicted band size: 81 kDa<br /> Observed band size: 81 kDa<br />](http://images.novusbio.com/fullsize/nbp3-26680_rabbit-cd44-mab-19h12-28220241136303.jpg)
![Immunocytochemistry/Immunofluorescence: CD44 Antibody (19H12) [NBP3-26680] - Staining of Hela with CD44 Antibody (19H12) 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 515-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26680_rabbit-cd44-mab-19h12-28220241323630.jpg)
![Flow Cytometry: CD44 Antibody (19H12) [NBP3-26680] - Overlay Peak curve showing Hela cells stained with CD44 Antibody (19H12) (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/nbp3-26680_rabbit-cd44-mab-19h12-282202414312756.jpg)
![Western Blot: PLK1 [p Thr210] Antibody [NBP1-78021] - Western blot analysis is shown to detect endogenous and recombinant protein present in HeLa cell lysates transfected with various plk-1 mutation constructs. Blots were reacted with anti-Plk-1 pT210 (panel A) and pan reactive anti-Plk-1 (panel B). Transfected cells were treated with 1 uM nocodazole followed by cell collection, lysate preparation, SDS-PAGE and western blotting. Using a 1:1000 dilution, anti-Plk-1 pT210 detects a single band corresponding to endogenous plk-1, but does not detect recombinant forms of the protein presumably because of a lack of phosphorylation in these mutants.](http://images.novusbio.com/fullsize/PLK1-[p-Thr210]-Antibody-Western-Blot-NBP1-78021-img0005.jpg "<b>Biological Strategies Validation. </b>Western Blot: PLK1 [p Thr210] Antibody [NBP1-78021] - Western blot analysis is shown to detect endogenous and recombinant protein present in HeLa cell lysates transfected with various plk-1 mutation constructs. Blots were reacted with anti-Plk-1 pT210 (panel A) and pan reactive anti-Plk-1 (panel B). Transfected cells were treated with 1 uM nocodazole followed by cell collection, lysate preparation, SDS-PAGE and western blotting. Using a 1:1000 dilution, anti-Plk-1 pT210 detects a single band corresponding to endogenous plk-1, but does not detect recombinant forms of the protein presumably because of a lack of phosphorylation in these mutants.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry: PLK1 [p Thr210] Antibody [NBP1-78021] - Used at a 1:200 dilution to detect Plk1 by immunohistochemistry in human breast carcinoma tumor tissue. Tissue was formalin-fixed and paraffin embedded.](http://images.novusbio.com/fullsize/PLK1-[p-Thr210]-Antibody-Immunohistochemistry-NBP1-78021-img0006.jpg)
![Western Blot: PLK1 [p Thr210] Antibody [NBP1-78021] - Plk-1 pT210 antibody to detect endogenous protein present in a Mouse A20 whole cell lysate (arrowhead). Comparison to a molecular weight marker indicates a band of ~68 kDa corresponding to Plk-1 protein. It is suggested to use a nuclear extract from synchronized cells to greatly increase the abundance of this protein in preparations. The blot was incubated with a 1:500 dilution of the antibody at room temperature followed by detection using standard techniques.](http://images.novusbio.com/fullsize/PLK1-[p-Thr210]-Antibody-Western-Blot-NBP1-78021-img0002.jpg)
![Immunohistochemistry: PLK1 [p Thr210] Antibody [NBP1-78021] - Used at a 1:200 dilution to detect Plk1 by immunohistochemistry in human colon carcinoma tumor tissue. Tissue was formalin-fixed and paraffin embedded.](http://images.novusbio.com/fullsize/PLK1-[p-Thr210]-Antibody-Immunohistochemistry-NBP1-78021-img0007.jpg)
![Western Blot: RSK1 [p Ser380] Antibody (1024F) [MAB79672] - Analysis of HeLa -/+ PMA cell lysates with 0.25 ug/ml of hRSK (S380) Monoclonal Antibody followed by HAF008. A specific band was detected for hRSK (S380) at approximately90 kDA (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.](http://images.novusbio.com/fullsize/RSK1-p-Ser380-Antibody-1024F-Western-Blot-MAB79672-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: RSK1 [p Ser380] Antibody (1024F) [MAB79672] - Analysis of HeLa -/+ PMA cell lysates with 0.25 ug/ml of hRSK (S380) Monoclonal Antibody followed by HAF008. A specific band was detected for hRSK (S380) at approximately90 kDA (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: RSK1 [p Ser380] Antibody (1024F) [MAB79672] - RSK1 [pSer380] was detected in immersion fixed HeLa cells treated with 200 nm of PMA using RSK1 [pSer380] Monoclonal Antibody at 1 ug/ml dilution. Cells were stained using the NorthernLights 557-conjugated Anti-Rabbit IgG Secondary Antibody (red) and counterstained with DAPI (blue). Specific staining was localized to the cytoplasm.](http://images.novusbio.com/fullsize/RSK1-p-Ser380-Antibody-1024F-Immunocytochemistry-Immunofluorescence-MAB79672-img0003.jpg)
![Western Blot: Myosin Phosphatase Antibody [NB110-38889] - Detection of human MYPT1 by western blot and immunoprecipitation. Samples: Whole cell lysate from HeLa (15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded), HEK293T (T; 50 ug) and Jurkat (J; 50 ug) cells. Antibodies: Affinity purified rabbit anti-MYPT1 antibody NB110-38889 (lot NB110-38889-2) used for WB at 0.4 ug/ml (A) and 1 ug/ml (B) and used for IP at 6 ug/mg lysate (B). MYPT1 was also immunoprecipitated by a previous lot (lot NB110-38889-1) of this antibody and by another rabbit anti-MYPT1 antibody, which recognizes a downstream epitope. Detection: Chemiluminescence with exposure times of 3 minutes (A) and 30 seconds (B).](http://images.novusbio.com/fullsize/Myosin-Phosphatase-Antibody-Western-Blot-NB110-38889-img0003.jpg "<b>Independent Antibodies Validation. </b>Western Blot: Myosin Phosphatase Antibody [NB110-38889] - Detection of human MYPT1 by western blot and immunoprecipitation. Samples: Whole cell lysate from HeLa (15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded), HEK293T (T; 50 ug) and Jurkat (J; 50 ug) cells. Antibodies: Affinity purified rabbit anti-MYPT1 antibody NB110-38889 (lot NB110-38889-2) used for WB at 0.4 ug/ml (A) and 1 ug/ml (B) and used for IP at 6 ug/mg lysate (B). MYPT1 was also immunoprecipitated by a previous lot (lot NB110-38889-1) of this antibody and by another rabbit anti-MYPT1 antibody, which recognizes a downstream epitope. Detection: Chemiluminescence with exposure times of 3 minutes (A) and 30 seconds (B).")
![Western Blot: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - Positive WB detected in: Jurkat whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate (treated with EGF or Pervanadate). All lanes: LAT antibody at 2.9ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 38 KDa. Observed band size: 38 KDa.](http://images.novusbio.com/fullsize/LAT-p-Tyr191-Antibody-2E4-Western-Blot-NBP3-15162-img0005.jpg "<b>Biological Strategies Validation. </b>Western Blot: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - Positive WB detected in: Jurkat whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate (treated with EGF or Pervanadate). All lanes: LAT antibody at 2.9ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 38 KDa. Observed band size: 38 KDa.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - Immunofluorescence staining of Hela cells with at LAT antibody 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 4°C. The secondary antibody was Alexa Fluor 488-congugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/LAT-p-Tyr191-Antibody-2E4-Immunocytochemistry-Immunofluorescence-NBP3-15162-img0001.jpg)
![Immunohistochemistry: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - IHC image of LAT antibody diluted at 1:100 and staining in paraffin-embedded human colon cancer. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/LAT-p-Tyr191-Antibody-2E4-Immunohistochemistry-NBP3-15162-img0004.jpg)
![Immunohistochemistry: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - IHC image of LAT antibody diluted at 1:100 and staining in paraffin-embedded human tonsil tissue. 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 30 minutes at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/LAT-p-Tyr191-Antibody-2E4-Immunohistochemistry-NBP3-15162-img0003.jpg)
![Immunoprecipitation: LAT [p Tyr191] Antibody (2E4) [NBP3-15162] - Immunoprecipitating LAT in A549 whole cell lysate. Lane 1: Rabbit control IgG (1ug) instead of LAT antibody in A549 whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: LAT antibody (3ug) + A549 whole cell lysate (1mg). Lane 3: A549 whole cell lysate (20ug).](http://images.novusbio.com/fullsize/LAT-p-Tyr191-Antibody-2E4-Immunoprecipitation-NBP3-15162-img0002.jpg)
![Immunoprecipitation: ATF4 Antibody (9E1) [NBP3-26497] - Immunoprecipitating ATF4 in Hela whole cell lysate.<br /> Lane 1: Rabbit control IgG instead of NBP3-26497 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000).<br /> Lane 2: NBP3-26497 (3ug) + Hela whole cell lysate (500ug).<br /> Lane 3: Hela whole cell lysate (20ug).<br />](http://images.novusbio.com/fullsize/nbp3-26497_rabbit-atf4-mab-9e1-26220241322155.jpg "Immunoprecipitation: ATF4 Antibody (9E1) [NBP3-26497] - Immunoprecipitating ATF4 in Hela whole cell lysate.<br /> Lane 1: Rabbit control IgG instead of NBP3-26497 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000).<br /> Lane 2: NBP3-26497 (3ug) + Hela whole cell lysate (500ug).<br /> Lane 3: Hela whole cell lysate (20ug).<br />")
![Immunohistochemistry: ATF4 Antibody (9E1) [NBP3-26497] - Image of ATF4 Antibody (9E1) diluted at 1:160 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26497_rabbit-atf4-mab-9e1-26220241510616.jpg)
![Western Blot: ATF4 Antibody (9E1) [NBP3-26497] - Positive Western Blot detected in: Hela whole cell lysate, MCF-7 whole cell lysate, 293 whole cell lysate, HepG2 whole cell lysate, Jurkat whole cell lysate, K562 whole cell lysate.<br /> All lanes: ATF4 Antibody at 1.6ug/ml.<br /> Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.<br /> Predicted band size: 39 KDa<br /> Observed band size: 50 KDa<br />](http://images.novusbio.com/fullsize/nbp3-26497_rabbit-atf4-mab-9e1-282202411472134.jpg)
![Immunocytochemistry/Immunofluorescence: ATF4 Antibody (9E1) [NBP3-26497] - Staining of HepG2 cells with ATF4 Antibody (9E1) at 1:53, 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/nbp3-26497_rabbit-atf4-mab-9e1-28220241312211.jpg)
![Flow Cytometry: ATF4 Antibody (9E1) [NBP3-26497] - Overlay histogram showing Hela cells stained with ATF4 Antibody (9E1) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.</p>](http://images.novusbio.com/fullsize/nbp3-26497_rabbit-atf4-mab-9e1-282202414312786.jpg)
![Western Blot: NPM1 Antibody [NBP2-27157] - Analysis of Nucleophosmin in human spleen tissue lysate in the 1) absence, 2) presence of immunizing peptide and 3) mouse spleen using NBP2-27204. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/NPM1-Antibody-Western-Blot-NBP2-27157-img0004.jpg "Western Blot: NPM1 Antibody [NBP2-27157] - Analysis of Nucleophosmin in human spleen tissue lysate in the 1) absence, 2) presence of immunizing peptide and 3) mouse spleen using NBP2-27204. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Immunohistochemistry-Paraffin: NPM1 Antibody [NBP2-27157] - Analysis of Nucleophosmin in formalin-fixed, paraffin-embedded human liver tissue using this antibody at 5 ug/ml.](http://images.novusbio.com/fullsize/NPM1-Antibody-Immunohistochemistry-Paraffin-NBP2-27157-img0003.jpg)
![Western Blot: TBK1 [p Ser 172] Antibody (SR2251) [NBP3-21592] - Western blot analysis using NBP3-21592 in (1) HeLa cell lysate; (2) HeLa cell treated with Calyculin A .](http://images.novusbio.com/fullsize/nbp3-21592_rabbit-tbk1-p-ser-172-mab-sr2251-57202317215195.jpg "<b>Biological Strategies Validation. </b>Western Blot: TBK1 [p Ser 172] Antibody (SR2251) [NBP3-21592] - Western blot analysis using NBP3-21592 in (1) HeLa cell lysate; (2) HeLa cell treated with Calyculin A .")