| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81074-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-27179-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-22380SS | |||
| Azide and BSA Free | NBP2-80842 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33064 | |||
![Western Blot: ULK3 Antibody (PSH01-09) [NBP3-33083] - Western blot analysis of ULK3 on different lysates with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/1,000 dilution. Lane 1: 293T cell lysate (20 ug/Lane) Lane 2: HeLa cell lysate (20 ug/Lane) Lane 3: Jurkat cell lysate (20 ug/Lane) Lane 4: Human brain tissue lysate (40 ug/Lane) Lane 5: Mouse brain tissue lysate (40 ug/Lane) Lane 6: Rat brain tissue lysate (40 ug/Lane) Predicted band size: 53 kDa Observed band size: 53 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-33083) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-33083_rabbit-ulk3-mab-psh01-09-28820241419159.jpg "Western Blot: ULK3 Antibody (PSH01-09) [NBP3-33083] - Western blot analysis of ULK3 on different lysates with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/1,000 dilution. Lane 1: 293T cell lysate (20 ug/Lane) Lane 2: HeLa cell lysate (20 ug/Lane) Lane 3: Jurkat cell lysate (20 ug/Lane) Lane 4: Human brain tissue lysate (40 ug/Lane) Lane 5: Mouse brain tissue lysate (40 ug/Lane) Lane 6: Rat brain tissue lysate (40 ug/Lane) Predicted band size: 53 kDa Observed band size: 53 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-33083) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: ULK3 Antibody (PSH01-09) [NBP3-33083] - Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-33083) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-33083_rabbit-ulk3-mab-psh01-09-298202414262625.jpg)
![Immunohistochemistry: ULK3 Antibody (PSH01-09) [NBP3-33083] - Immunofluorescence analysis of paraffin-embedded human testis tissue labeling ULK3 with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-33083, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-33083_rabbit-ulk3-mab-psh01-09-298202414161889.jpg)
![Immunocytochemistry/ Immunofluorescence: ULK3 Antibody (PSH01-09) [NBP3-33083] - Immunocytochemistry analysis of HeLa cells labeling ULK3 with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-ULK3 antibody (NBP3-33083) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-33083_rabbit-ulk3-mab-psh01-09-29202410484852.jpg)
![Flow Cytometry: ULK3 Antibody (PSH01-09) [NBP3-33083] - Flow cytometric analysis of HeLa cells labeling ULK3. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-33083, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-33083_rabbit-ulk3-mab-psh01-09-39202488469.jpg)
![Western Blot: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Western blot analysis of Cytokeratin 1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Western-Blot-NBP2-67681-img0003.jpg "Western Blot: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Western blot analysis of Cytokeratin 1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat")
![Immunohistochemistry-Paraffin: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Analysis of paraffin-embedded rat skin tissue with Rabbit anti-Cytokeratin 1 antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Immunohistochemistry-Paraffin-NBP2-67681-img0006.jpg)
![Western Blot: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Analysis of Cytokeratin 1 on different lysates using anti-Cytokeratin 1 antibody at 1/1,000 dilution. Positive control: Lane 1: 293T Lane 2: Hela](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Western-Blot-NBP2-67681-img0002.jpg)
![Immunohistochemistry-Paraffin: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Analysis of paraffin-embedded mouse skin tissue using anti-Cytokeratin 1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Immunohistochemistry-Paraffin-NBP2-67681-img0001.jpg)
![Immunohistochemistry-Paraffin: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Immunofluorescence analysis of paraffin-embedded human skin tissue labeling Cytokeratin 1 (washed with PBS. And then probed with the primary antibodies Cytokeratin 1 (red) at 1/200 dilution and Vimentin (green) at 1/200 dilution at +4 overnight, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor(TM) 594) and Goat Anti-Mouse IgG H&L (iFluor(TM) 488) were used as the secondary antibodies at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Immunohistochemistry-Paraffin-NBP2-67681-img0004.jpg)
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: Cytokeratin 1 Antibody (SN72-08) [NBP2-67681] - Analysis of paraffin-embedded human skin tissue using anti-Cytokeratin 1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/400) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/Cytokeratin-1-Antibody-SN72-08-Immunohistochemistry-Paraffin-NBP2-67681-img0005.jpg)
![Western Blot: STK33 Antibody (6G1) [H00065975-M02] - STK33 monoclonal antibody (M02), clone 6G1 Analysis of STK33 expression in HeLa.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Western-Blot-H00065975-M02-img0010.jpg "Western Blot: STK33 Antibody (6G1) [H00065975-M02] - STK33 monoclonal antibody (M02), clone 6G1 Analysis of STK33 expression in HeLa.")
![Immunocytochemistry/Immunofluorescence: STK33 Antibody (6G1) [H00065975-M02] - Analysis of monoclonal antibody to STK33 on HeLa cell. Antibody concentration 25 ug/ml.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Immunocytochemistry-Immunofluorescence-H00065975-M02-img0006.jpg)
![Western Blot: STK33 Antibody (6G1) [H00065975-M02] - Analysis of STK33 over-expressed 293 cell line, cotransfected with STK33 Validated Chimera RNAi ( Cat # H00065975-R01V ) (Lane 2) or non-transfected control (Lane 1). Blot probed with STK33 monoclonal antibody (M02) clone 6G1 (Cat # H00065975-M02 ). GAPDH ( 36.1 kDa ) used as specificity and loading control.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Western-Blot-H00065975-M02-img0008.jpg)
![Western Blot: STK33 Antibody (6G1) [H00065975-M02] - Analysis of STK33 expression in transfected 293T cell line by STK33 monoclonal antibody (M02), clone 6G1.Lane 1: STK33 transfected lysate(57.9 KDa).Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Western-Blot-H00065975-M02-img0011.jpg)
![Immunoprecipitation: STK33 Antibody (6G1) [H00065975-M02] - Analysis of STK33 transfected lysate using anti-STK33 monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with STK33 MaxPab rabbit polyclonal antibody.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Immunoprecipitation-H00065975-M02-img0007.jpg)
![Sandwich ELISA: STK33 Antibody (6G1) [H00065975-M02] - Detection limit for recombinant GST tagged STK33 is 1 ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/STK33-Antibody-6G1-Sandwich-ELISA-H00065975-M02-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: TrkA Antibody (MNAC13) [NBP2-81074] - Immunofluoresence staining of fixed HeLa cells with anti-TrkA antibody (MNAC13) [NBP2-81074]. Immunofluorescence analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton stained with the chimeric rabbit IgG version of MNAC13 [NBP2-81074] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81074, DAPI, merged channels and a negative control. The negative control was stained with unimmunized rabbit IgG followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/TrkA-Antibody-MNAC13-Immunocytochemistry-Immunofluorescence-NBP2-81074-img0001.jpg "Immunocytochemistry/Immunofluorescence: TrkA Antibody (MNAC13) [NBP2-81074] - Immunofluoresence staining of fixed HeLa cells with anti-TrkA antibody (MNAC13) [NBP2-81074]. Immunofluorescence analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton stained with the chimeric rabbit IgG version of MNAC13 [NBP2-81074] at 10 ug/ml for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/ml), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81074, DAPI, merged channels and a negative control. The negative control was stained with unimmunized rabbit IgG followed by Alexa Fluor 488 secondary antibody.")
![Western Blot: PKC theta Antibody (M217) [NBP3-23308] - Western blot analysis of PKC theta in human Jurkat cell lysate. The blot was probed with anti-PKC theta at 1:250 (lane 1) and 1:1000 (lane 2).](http://images.novusbio.com/fullsize/nbp3-23308_mouse-pkc-theta-mab-m217-19920231992823.jpg "Western Blot: PKC theta Antibody (M217) [NBP3-23308] - Western blot analysis of PKC theta in human Jurkat cell lysate. The blot was probed with anti-PKC theta at 1:250 (lane 1) and 1:1000 (lane 2).")
![Immunocytochemistry/Immunofluorescence: PKC theta Antibody (M217) [NBP3-23308] - Immunocytochemical labeling of PKC theta in rat PC12 cells differentiated with NGF. The cells were labeled with mouse monoclonal PKC theta (N-terminal region) antibody, then detected using appropriate secondary antibody conjugated to Cy3.](http://images.novusbio.com/fullsize/nbp3-23308_mouse-pkc-theta-mab-m217-19920231410124.jpg)
![Immunohistochemistry: TRBC1 Antibody (5A8A10) [NBP3-27179] - Analysis of paraffin-embedded spleen tissues using TRBC1 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/nbp3-27179_mouse-trbc1-mab-5a8a10-bsa-free-104202491586.jpg%3Fv=1666706084 "Immunohistochemistry: TRBC1 Antibody (5A8A10) [NBP3-27179] - Analysis of paraffin-embedded spleen tissues using TRBC1 mouse mAb with DAB staining.")
![Western Blot: TRBC1 Antibody (5A8A10) [NBP3-27179] - Analysis using TRBC1 mAb against HEK293-6e (1) and TRBC1 (AA: 1-149)-hIgGFc transfected HEK293-6e (2) cell lysate.](http://images.novusbio.com/fullsize/nbp3-27179_mouse-trbc1-mab-5a8a10-bsa-free-1042024917023.jpg%3Fv=1666706084)
![ELISA: TRBC1 Antibody (5A8A10) [NBP3-27179] - Black line: Control Antigen (100 ng); Purple line: Antigen (10 ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng)](http://images.novusbio.com/fullsize/nbp3-27179_mouse-trbc1-mab-5a8a10-bsa-free-1042024915814.jpg%3Fv=1666706084)
![Flow Cytometry: TRBC1 Antibody (5A8A10) [NBP3-27179] - Analysis of JURKAT cells using TRBC1 mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/nbp3-27179_mouse-trbc1-mab-5a8a10-bsa-free-10420249141920.jpg%3Fv=1666706084)
![Western Blot: TRBC1 Antibody (5A8A10) [NBP3-27179] - Analysis using TRBC1 mAb against human TRBC1 (AA: 1-149) recombinant protein. (Expected MW is 42.8 kDa)](http://images.novusbio.com/fullsize/nbp3-27179_mouse-trbc1-mab-5a8a10-bsa-free-10420249181948.jpg%3Fv=1666706084)
![Western Blot: PKC delta Antibody (M242) [NBP3-23307] - Western blot analysis of adult mouse brain tissue lysate. The blot was probed with mouse monoclonal anti-PKC delta (N-terminal region) at 1:125 (lane 1) and 1:500 (lane 2).](http://images.novusbio.com/fullsize/nbp3-23307_mouse-pkc-delta-mab-m242-18920231735527.jpg "Western Blot: PKC delta Antibody (M242) [NBP3-23307] - Western blot analysis of adult mouse brain tissue lysate. The blot was probed with mouse monoclonal anti-PKC delta (N-terminal region) at 1:125 (lane 1) and 1:500 (lane 2).")
![Immunocytochemistry/Immunofluorescence: PKC delta Antibody (M242) [NBP3-23307] - Immunocytochemical labeling of PKC delta in rat PC12 cells differentiated with NGF. The cells were labeled with mouse monoclonal PKC delta (N-terminal region) antibody, then detected using appropriate secondary antibody conjugated to Cy3.](http://images.novusbio.com/fullsize/nbp3-23307_mouse-pkc-delta-mab-m242-1192023166534.jpg)
![Western Blot: JNK2 Antibody [NBP1-30905] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with JNK2 antibody [N1C3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/JNK2-Antibody-Western-Blot-NBP1-30905-img0007.jpg "Western Blot: JNK2 Antibody [NBP1-30905] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with JNK2 antibody [N1C3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: JNK2 Antibody [NBP1-30905] - Analysis of methanol-fixed MCF-7, using antibody at 1:200 dilution.](http://images.novusbio.com/fullsize/JNK2-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-30905-img0002.jpg)
![Immunohistochemistry-Paraffin: JNK2 Antibody [NBP1-30905] - Paraffin-embedded N87 xenograft, using antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/JNK2-Antibody-Immunohistochemistry-Paraffin-NBP1-30905-img0003.jpg)
![Western Blot: JNK2 Antibody [NBP1-30905] - Sample (30 ug of whole cell lysate) A: MCF-7 10% SDS PAGE; antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/JNK2-Antibody-Western-Blot-NBP1-30905-img0004.jpg)
![Western Blot: JNK2 Antibody [NBP1-30905] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with JNK2 antibody [N1C3] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/JNK2-Antibody-Western-Blot-NBP1-30905-img0006.jpg)
![Western Blot: MAVS Antibody (58N3B6) [NBP2-22380] - Analysis of A) partial recombinant protein and B) human HeLa lysate using MAVS antibody at 0.1 ug/ml and 2 ug/ml, respectively. Goat anti-mouse Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/MAVS-Antibody-58N3B6-Western-Blot-NBP2-22380-img0003.jpg "Western Blot: MAVS Antibody (58N3B6) [NBP2-22380] - Analysis of A) partial recombinant protein and B) human HeLa lysate using MAVS antibody at 0.1 ug/ml and 2 ug/ml, respectively. Goat anti-mouse Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Immunohistochemistry-Paraffin: MAVS Antibody (58N3B6) [NBP2-22380] - Normal human spleen tissue stained with MAVS (IPS-1) antibody (3 ug/ml), peroxidase-conjugate and DAB chromogen.](http://images.novusbio.com/fullsize/MAVS-Antibody-58N3B6-Immunohistochemistry-Paraffin-NBP2-22380-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - ICC/IF staining of MCF-7 cells with followed by goat anti-Mouse IgG-CF488 (Green). Nuclei are stained with Red Dot (Red).](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-HRB2-451-Immunocytochemistry-Immunofluorescence-NBP2-29437-img0009.jpg "Immunocytochemistry/Immunofluorescence: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - ICC/IF staining of MCF-7 cells with followed by goat anti-Mouse IgG-CF488 (Green). Nuclei are stained with Red Dot (Red).")
![Flow Cytometry: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - Flow Cytometric Analysis of human trypsinized MCF-7 cells. ErbB2/Her2 Monospecific Mouse Monoclonal Antibody (HRB2/451) followed by goat anti-Mouse IgG-CF488 (Blue); Isotype control (Red).](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-HRB2-451-Flow-Cytometry-NBP2-29437-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - Immunofluorescent staining of PFA-fixed MCF-7 cells with ErbB2/Her2 Monospecific Mouse Monoclonal Antibody (HRB2/451) followed by goat anti-Mouse IgG-CF488 (Green). Nuclei are stained with Reddot (Red).](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-HRB2-451-Immunocytochemistry-Immunofluorescence-NBP2-29437-img0011.jpg)
![Flow Cytometry: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - Flow Cytometric Analysis of human trypsinized SK-BR3 cells. ErbB2/Her2 Antibody (HRB2/451) followed by Goat anti-Mouse IgG-CF488 (Blue); Isotype control (Red).](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-HRB2-451-Flow-Cytometry-NBP2-29437-img0008.jpg)
![Protein Array: ErbB2/Her2 Antibody (HRB2/451) [NBP2-29437] - Analysis of Protein Array containing more than 19,000 full-length human proteins using ErbB2/Her2 Antibody (HRB2/451) Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (MAb) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProt(TM) array. Z-scores are described in units of standard deviations (SD?s) above the mean value of all signals generated on that array. If targets on HuProt(TM) are arranged in descending order of the Z-score, the S-score is the difference (also in units of SD?s) between the Z-score. S-score therefore represents the relative target specificity of a MAb to its intended target. A MAb is considered to specific to its intended target, if the MAb has an S-score of at least 2.5.](http://images.novusbio.com/fullsize/ErbB2-Her2-Antibody-HRB2-451-Protein-Array-NBP2-29437-img0010.jpg)
![Western Blot: MAST1 Antibody [NBP2-17228] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with MAST1 antibody [N2N3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/MAST1-Antibody-Western-Blot-NBP2-17228-img0006.jpg "Western Blot: MAST1 Antibody [NBP2-17228] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with MAST1 antibody [N2N3] diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![Western Blot: MAST1 Antibody [NBP2-17228] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 5% SDS PAGE gel, diluted at 1:500.](http://images.novusbio.com/fullsize/MAST1-Antibody-Western-Blot-NBP2-17228-img0004.jpg)
![Immunohistochemistry-Paraffin: Activin RIIB Antibody [NBP2-15268] - Activin Receptor Type IIB antibody [N1C1] detects Activin Receptor Type IIB protein at cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded mouse placenta. Activin Receptor Type IIB stained by Activin Receptor Type IIB antibody [N1C1] diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/Activin-RIIB-Antibody-Immunohistochemistry-Paraffin-NBP2-15268-img0008.jpg "Immunohistochemistry-Paraffin: Activin RIIB Antibody [NBP2-15268] - Activin Receptor Type IIB antibody [N1C1] detects Activin Receptor Type IIB protein at cytoplasm by immunohistochemical analysis. Sample: Paraffin-embedded mouse placenta. Activin Receptor Type IIB stained by Activin Receptor Type IIB antibody [N1C1] diluted at 1:500. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![Western Blot: Activin RIIB Antibody [NBP2-15268] - Mouse tissue extract (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with Activin Receptor Type IIB antibody [N1C1] diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Activin-RIIB-Antibody-Western-Blot-NBP2-15268-img0006.jpg)
![Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Activin Receptor Type IIB antibody [N1C1] (NBP2-15268) diluted at 1:25000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-15268_rabbit-polyclonal-activin-riib-antibody-western-blot-261120251820472.jpg)
![Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Activin Receptor Type IIB antibody [N1C1] (NBP2-15268) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-15268_rabbit-polyclonal-activin-riib-antibody-western-blot-2611202518351720.jpg)