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![Western Blot: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of 25 ug of various whole cell lysates or 0.5 ug of purified protein (full-length His-RhoA, truncated GST-RhoB or full-length GST-RhoC fusion) per well onto a 4-20% Tris-HCl polyacrylamide gel.](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Western-Blot-NBP2-22528-img0001.jpg "Western Blot: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of 25 ug of various whole cell lysates or 0.5 ug of purified protein (full-length His-RhoA, truncated GST-RhoB or full-length GST-RhoC fusion) per well onto a 4-20% Tris-HCl polyacrylamide gel.")
![Immunocytochemistry/Immunofluorescence: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of Rho A/B/C (green) showing staining in the in the cytoplasm of A431 cells (right) compared to a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunocytochemistry-Immunofluorescence-NBP2-22528-img0005.jpg)
![Immunohistochemistry-Paraffin: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis showing staining in the cytoplasm of human hepatocarcinoma (right) compared with a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunohistochemistry-Paraffin-NBP2-22528-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of RhoA/B/C (green) in NIH3T3 cells. Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% BSA/TBST for 15 minutes at room temperature. Cells were probed with a RhoA/B/C monoclonal antibody at a dilution of 1:100 for at least 1 hour at room temperature, washed with PBS, and incubated with DyLight 488-conjugated goat-anti-mouse IgG secondary antibody at a dilution of 1:400 for 30 minutes at room temperature. Nuclei (blue) were stained with Hoechst 33342 dye.](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunocytochemistry-Immunofluorescence-NBP2-22528-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of Rho A/B/C (green) showing staining in the in the cytoplasm of NIH-3T3 cells (right) compared to a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunocytochemistry-Immunofluorescence-NBP2-22528-img0004.jpg)
![Immunohistochemistry-Paraffin: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of showing staining in the cytoplasm of mouse breast tissue (right) compared with a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunohistochemistry-Paraffin-NBP2-22528-img0006.jpg)
![Immunohistochemistry-Paraffin: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis showing staining in the cytoplasm of human prostate carcinoma (right) compared with a negative control without primary antibody (left).](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunohistochemistry-Paraffin-NBP2-22528-img0007.jpg)
![Immunoprecipitation: RhoA Antibody (1A11-4G10) [NBP2-22528] - Analysis of RhoA/B/C was performed on HeLa cells. Antigen-antibody complexes were formed by incubating 750 ug of HeLa cell lysate with 2 ug of a RhoA/B/C monoclonal antibody overnight on a rocking platform at 4C. The immune complexes were captured on 50 ul Protein A/G Plus Agarose, washed extensively, and eluted with 5X Lane Marker Reducing Sample Buffer. Eluted sample (right lane) and 25 ug of HeLa cell lysate (left lane) were resolved on a 4-20% Tris-HCl polyacrylamide gel, transferred to a PVDF membrane, and blocked with 5% BSA/TBS-0.1%Tween for at least 1 hour. The membrane was probed with a Rho A/B/C monoclonal antibody at a dilution of 1:1000 overnight rotating at 4C, washed in TBST, and probed with Clean-blot IP Detection Reagent at a dilution of 1:2500 for at least 1 hour.](http://images.novusbio.com/fullsize/RhoA-Antibody-1A11-4G10-Immunoprecipitation-NBP2-22528-img0002.jpg)
![Western Blot: CDCA7L Antibody (OTI3B5) [NBP2-46198] - Detection of CDCA7L by western blot. Samples: Whole cell lysate from prostate cancer; 40 ug. Antibodies:CDCA7L Antibody [NBP2-46198] at dilutions 1:500, 1:1000, 1:2000. Detection: Chemiluminescence with exposure of 5 seconds. Image from verified customer review.](http://images.novusbio.com/fullsize/CDCA7L-Antibody-OTI3B5-Western-Blot-NBP2-46198-img0010.jpg "Western Blot: CDCA7L Antibody (OTI3B5) [NBP2-46198] - Detection of CDCA7L by western blot. Samples: Whole cell lysate from prostate cancer; 40 ug. Antibodies:CDCA7L Antibody [NBP2-46198] at dilutions 1:500, 1:1000, 1:2000. Detection: Chemiluminescence with exposure of 5 seconds. Image from verified customer review.")
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Human tonsil tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0007.jpg)
![Western Blot: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CDCA7L.](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Western-Blot-NBP2-46198-img0008.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Adenocarcinoma of Human breast tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0001.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Human colon tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0002.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Carcinoma of Human kidney tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0003.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Adenocarcinoma of Human ovary tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0004.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Human pancreas tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0005.jpg)
![Immunohistochemistry: CDCA7L Antibody (3B5) [NBP2-46198] - Analysis of Human lymphoma tissue. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120C for 3min)](http://images.novusbio.com/fullsize/CDCA7L-Antibody-3B5-Immunohistochemistry-NBP2-46198-img0006.jpg)
![Western Blot: TIMP2 Antibody (1A6) [NBP2-01573] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TIMP2 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-TIMP2.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Western-Blot-NBP2-01573-img0003.jpg "Western Blot: TIMP2 Antibody (1A6) [NBP2-01573] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TIMP2 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-TIMP2.")
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Human pancreas tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0010.jpg)
![Flow Cytometry: TIMP2 Antibody (1A6) [NBP2-01573] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-TIMP2 antibody, and then analyzed by flow cytometry.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Flow-Cytometry-NBP2-01573-img0002.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Adenocarcinoma of Human breast tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0004.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Adenocarcinoma of Human endometrium tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0005.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Adenocarcinoma of Human ovary tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0006.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Carcinoma of Human lung tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0007.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Human breast tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0008.jpg)
![Immunohistochemistry-Paraffin: TIMP2 Antibody (1A6) [NBP2-01573] - Staining of paraffin-embedded Human endometrium tissue using anti-TIMP2 mouse monoclonal antibody.](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Immunohistochemistry-Paraffin-NBP2-01573-img0009.jpg)
![Flow Cytometry: TIMP2 Antibody (1A6) [NBP2-01573] - Analysis of Jurkat cells, using anti-TIMP2 antibody, (Red), compared to a nonspecific negative control antibody (Blue).](http://images.novusbio.com/fullsize/TIMP2-Antibody-1A6-Flow-Cytometry-NBP2-01573-img0001.jpg)
![Western Blot: Androgen R/NR3C4 Antibody [NB100-1446] - Staining of Human Cerebellum (A) and (0.1ug/ml) negative control Pancreas (B) lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Androgen-R-NR3C4-Antibody-Western-Blot-NB100-1446-img0008.jpg "Western Blot: Androgen R/NR3C4 Antibody [NB100-1446] - Staining of Human Cerebellum (A) and (0.1ug/ml) negative control Pancreas (B) lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: Androgen R/NR3C4 Antibody [NB100-1446] - Analysis of paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing Mitochondrial/cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](http://images.novusbio.com/fullsize/Androgen-R-NR3C4-Antibody-Immunocytochemistry-Immunofluorescence-NB100-1446-img0010.jpg)
![Immunohistochemistry-Paraffin: Androgen R/NR3C4 Antibody [NB100-1446] - (2ug/ml) staining of paraffin embedded Human Prostate. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/Androgen-R-NR3C4-Antibody-Immunohistochemistry-Paraffin-NB100-1446-img0006.jpg)
![Chromatin Immunoprecipitation: Androgen R/NR3C4 Antibody [NB100-1446] - (Protein G) measuring FKBP5 enrichment.](http://images.novusbio.com/fullsize/Androgen-R-NR3C4-Antibody-Chromatin-Immunoprecipitation-NB100-1446-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: Androgen R/NR3C4 Antibody [NB100-1446] - Analysis of paraformaldehyde fixed MCF7 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing Mitochondrial/cytoplasmic staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2ug/ml).](http://images.novusbio.com/fullsize/Androgen-R-NR3C4-Antibody-Immunocytochemistry-Immunofluorescence-NB100-1446-img0009.jpg)
![Immunohistochemistry-Paraffin: Goat Polyclonal Androgen R/NR3C4 Antibody [IMGENEX: IMG-3238] [NB100-1446] - Androgen receptor immunoreactivity in equine epididymis. NB100-1446 was diluted to 1 ug/mL and left on tissue sections for 30 min at room temperature. Immunoreactivity was best demonstrated with heat induced epitope retrieval using an EDTA based solution. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nb100-1446_goat-polyclonal-androgen-r-nr3c4-antibody-imgenex-img-3238-immunohistochemistry-paraffin-7112023153914.jpg)
![Immunohistochemistry-Paraffin: Goat Polyclonal Androgen R/NR3C4 Antibody [IMGENEX: IMG-3238] [NB100-1446] - Androgen receptor immunoreactivity in canine epididymis. NB100-1446 was diluted to 1 ug/mL and left on tissue sections for 30m at room temperature. Immunoreactivity was best demonstrated with heat induced epitope retrieval in an EDTA based buffer. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nb100-1446_goat-polyclonal-androgen-r-nr3c4-antibody-imgenex-img-3238-immunohistochemistry-paraffin-711202315446..jpg)
![Immunohistochemistry-Paraffin: Goat Polyclonal Androgen R/NR3C4 Antibody [IMGENEX: IMG-3238] [NB100-1446] - Androgen receptor immunoreactivity in feline epididymis. NB100-1446 was diluted to 1 ug/mL and left on tissue sections for 30m at room temperature. Immunoreactivity was best demonstrated with heat induced epitope retrieval in an EDTA based buffer. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nb100-1446_goat-polyclonal-androgen-r-nr3c4-antibody-imgenex-img-3238-immunohistochemistry-paraffin-7112023154738..png)
![Immunohistochemistry-Paraffin: Goat Polyclonal Androgen R/NR3C4 Antibody [IMGENEX: IMG-3238] [NB100-1446] - Androgen receptor immunoreactivity in mouse testis. NB100-1446 was diluted to 1 ug/mL and left on tissue sections for 30m at room temperature. Immunoreactivity was best demonstrated with heat induced epitope retrieval in an EDTA based buffer. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nb100-1446_goat-polyclonal-androgen-r-nr3c4-antibody-imgenex-img-3238-immunohistochemistry-paraffin-7112023155323..png)
![Immunohistochemistry-Paraffin: Goat Polyclonal Androgen R/NR3C4 Antibody [IMGENEX: IMG-3238] [NB100-1446] - Androgen receptor immunoreactivity in human testis. NB100-1446 was diluted to 1ug per mL and left on tissue sections for 30m at room temperature. Immunoreactivity was best demonstrated with heat-induced epitope retrieval in an EDTA-based solution. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nb100-1446_goat-polyclonal-androgen-r-nr3c4-antibody-imgenex-img-3238-immunohistochemistry-paraffin-4122023141337..jpg)
![Western Blot: TMPRSS2 Antibody [NBP1-20984] - Western blot analysis of Human pancreas and kidney lysates (35 ug protein in RIPA buffer). Antibody at 0.5 ug/mL. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/TMPRSS2-Antibody-Western-Blot-NBP1-20984-img0005.jpg "Western Blot: TMPRSS2 Antibody [NBP1-20984] - Western blot analysis of Human pancreas and kidney lysates (35 ug protein in RIPA buffer). Antibody at 0.5 ug/mL. Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: TMPRSS2 Antibody [NBP1-20984] - Negative Control showing staining of paraffin embedded Human Kidney, with no primary antibody.](http://images.novusbio.com/fullsize/TMPRSS2-Antibody-Immunohistochemistry-Paraffin-NBP1-20984-img0007.jpg)
![Immunohistochemistry-Paraffin: TMPRSS2 Antibody [NBP1-20984] - Staining of paraffin embedded Human Kidney. Antibody at 8 ug/mL. Heat induced antigen retrieval with citrate buffer pH 6, HRP-staining.](http://images.novusbio.com/fullsize/TMPRSS2-Antibody-Immunohistochemistry-Paraffin-NBP1-20984-img0006.jpg)
![Simple Western: TMPRSS2 Antibody [NBP1-20984] - Simple Western lane view (A) and electropherogram view (B) show recombinant human TMPRSS2 Protein (Catalog # H00007113-Q01) loaded at a serial dilution. A specific band was detected for TMPRSS2 at approximately 45 kDa (as indicated) using 1:50 of Goat Polyclonal (Catalog # NBP1-20984). (C) The calculated dynamic range had an R-squared value of 0.9997 with assay sensitivity down to 6.2 ng/mL. This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.](http://images.novusbio.com/fullsize/TMPRSS2-Antibody-Simple-Western-NBP1-20984-img0008.jpg)
![Western Blot: AKT1 Antibody (3A3) [NBP1-51602] - Analysis using AKT1 antibody against NIH/3T3 (1), Hela (2),COS7 (3) and Jurkat (4) cell lysate.](http://images.novusbio.com/fullsize/Akt1-Antibody-3A3-Western-Blot-NBP1-51602-img0006.jpg "Western Blot: AKT1 Antibody (3A3) [NBP1-51602] - Analysis using AKT1 antibody against NIH/3T3 (1), Hela (2),COS7 (3) and Jurkat (4) cell lysate.")
![Immunohistochemistry-Paraffin: AKT1 Antibody (3A3) [NBP1-51602] - Analysis of human breast carcinoma using AKT1 antibody at 1:50. IHC-P image submitted by a verified customer review.](http://images.novusbio.com/fullsize/Akt1-Antibody-3A3-Immunohistochemistry-Paraffin-NBP1-51602-img0010.jpg)
![Western Blot: AKT1 Antibody (3A3) [NBP1-51602] - Analysis of extracts from COS cells using AKT1 antibody at 1:1000. WB image submitted by a verified customer review.](http://images.novusbio.com/fullsize/Akt1-Antibody-3A3-Western-Blot-NBP1-51602-img0008.jpg)
![Immunohistochemistry-Paraffin: AKT1 Antibody (3A3) [NBP1-51602] - Analysis of human endometrial cancer using AKT1 antibody at 1:25. IHC-P image submitted by a verified customer review.](http://images.novusbio.com/fullsize/Akt1-Antibody-3A3-Immunohistochemistry-Paraffin-NBP1-51602-img0009.jpg)
![Immunohistochemistry-Paraffin: N-Cadherin Antibody (5D5) [NBP1-51612] - Analysis of human lung cancer (A), colon cancer (B), ovarian cancer (C) and mammary cancer(D), using CDH2 mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-5D5-Immunohistochemistry-Paraffin-NBP1-51612-img0015.jpg "Immunohistochemistry-Paraffin: N-Cadherin Antibody (5D5) [NBP1-51612] - Analysis of human lung cancer (A), colon cancer (B), ovarian cancer (C) and mammary cancer(D), using CDH2 mouse mAb with DAB staining.")
![Western Blot: N-Cadherin Antibody (5D5) [NBP1-51612] - Analysis using CDH2 mouse mAb against A431 (1), NIH/3T3 (2), Hela (3), C6 (4) and LNCap (5) cell lysate.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-5D5-Western-Blot-NBP1-51612-img0016.jpg)
![Immunocytochemistry/Immunofluorescence: N-Cadherin Antibody (5D5) [NBP1-51612] - Immunofluorescence analysis of A431 cells using CDH2 mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-5D5-Immunocytochemistry-Immunofluorescence-NBP1-51612-img0012.jpg)
![Flow Cytometry: N-Cadherin Antibody (5D5) [NBP1-51612] - Analysis of PC-2 cells using CDH2 mouse mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-5D5-Flow-Cytometry-NBP1-51612-img0011.jpg)
![Immunohistochemistry-Paraffin: N-Cadherin Antibody (5D5) [NBP1-51612] - Analysis of human Placenta tissues using CDH2 mouse mAb](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-5D5-Immunohistochemistry-Paraffin-NBP1-51612-img0014.jpg)
![Western Blot: CBL Antibody (3B12) [NBP2-37574] - Western blot analysis using C-CBL mouse mAb against RAJI (1), RAW264.7 (2), K562 (3), SKBR-3 (4), 3T3-L1 (5), THP-1 (6) and PC-12 (7) cell lysate.](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Western-Blot-NBP2-37574-img0003.jpg "Western Blot: CBL Antibody (3B12) [NBP2-37574] - Western blot analysis using C-CBL mouse mAb against RAJI (1), RAW264.7 (2), K562 (3), SKBR-3 (4), 3T3-L1 (5), THP-1 (6) and PC-12 (7) cell lysate.")
![Immunocytochemistry/Immunofluorescence: CBL Antibody (3B12) [NBP2-37574] - Immunofluorescence analysis of Hela cells using C-CBL mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin.](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Immunocytochemistry-Immunofluorescence-NBP2-37574-img0004.jpg)
![Immunohistochemistry-Paraffin: CBL Antibody (3B12) [NBP2-37574] - Analysis of cancer tissues using C-CBL mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Immunohistochemistry-NBP2-37574-img0007.jpg)
![Flow Cytometry: CBL Antibody (3B12) [NBP2-37574] - Flow cytometric analysis of MCF-7 cells using C-CBL mouse mAb (blue) and negative control (red).](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Flow-Cytometry-NBP2-37574-img0005.jpg)
![Western Blot: CBL Antibody (3B12) [NBP2-37574] - Western blot analysis using C-CBL mAb against human C-CBL (AA: 684-865) recombinant protein. (Expected MW is 44.9 kDa)](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Western-Blot-NBP2-37574-img0002.jpg)
![Immunohistochemistry-Paraffin: CBL Antibody (3B12) [NBP2-37574] - Analysis of ovarian cancer tissues using C-CBL mouse mAb with DAB staining.](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-Immunohistochemistry-NBP2-37574-img0006.jpg)
![ELISA: CBL Antibody (3B12) [NBP2-37574] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/CBL-Antibody-3B12-ELISA-NBP2-37574-img0001.jpg)
![Immunohistochemistry: BCMA/TNFRSF17 Antibody (Vicky-1) [NBP1-97637] - Immunostaining of HEK 293 cells transfected with a human BCMA expression plasmid (left panel), or mock transfected (right panel). Method: 3 days after transfection of cells with the indicated constructs, cells were fixed with acetone or 4% formaldehyde for 5 min. at room temperature. Slides were blocked with normal IgG, and incubated for 1 hour with 5ug/ml MAb to BCMA (human) (Vicky-1) in 1% BSA in 1x PBS. After washes in PBS, samples were incubated with the secondary antibody for 1 hour, washed in PBS and revealed with StreptABComplex/HRP (Vector) and AEC.](http://images.novusbio.com/fullsize/BCMA-TNFRSF17-Antibody-Vicky-1-Immunohistochemistry-NBP1-97637-img0007.jpg "Immunohistochemistry: BCMA/TNFRSF17 Antibody (Vicky-1) [NBP1-97637] - Immunostaining of HEK 293 cells transfected with a human BCMA expression plasmid (left panel), or mock transfected (right panel). Method: 3 days after transfection of cells with the indicated constructs, cells were fixed with acetone or 4% formaldehyde for 5 min. at room temperature. Slides were blocked with normal IgG, and incubated for 1 hour with 5ug/ml MAb to BCMA (human) (Vicky-1) in 1% BSA in 1x PBS. After washes in PBS, samples were incubated with the secondary antibody for 1 hour, washed in PBS and revealed with StreptABComplex/HRP (Vector) and AEC.")
![Flow Cytometry: BCMA/TNFRSF17 Antibody (Vicky-1) [NBP1-97637] - Analysis using the PE conjugate of NBP1-97637. Staining of 10^6 U266 cells using BCMA (human), mAb (Vicky-1) (PE conjugate) at a concentration of 10ug/ml.](http://images.novusbio.com/fullsize/BCMA-TNFRSF17-Antibody-Vicky-1-Flow-Cytometry-NBP1-97637-img0011.jpg)
![Flow Cytometry: BCMA/TNFRSF17 Antibody (Vicky-1) [NBP1-97637] - Detection of endogenous human BCMA with MAb to BCMA (human) (Vicky-1). Method: U266 cells (2x10^5) were incubated on ice for 30 min. with 0.2ug of MAb to BCMA (human) (Vicky-1) or an isotype control in 25ul FACS buffer (PBS, 5% fetal calf serum, 0.02% azide). The primary antibody was revealed with PAb to Rat IgG (R-PE) and then analyzed by flow cytometry.](http://images.novusbio.com/fullsize/BCMA-TNFRSF17-Antibody-Vicky-1-Flow-Cytometry-NBP1-97637-img0006.jpg)
![Flow Cytometry: BCMA/TNFRSF17 Antibody (Vicky-1) [NBP1-97637] - Analysis using the FITC conjugate of NBP1-97637. Staining of 10^6 Jurkat cells using BCMA (human), mAb (Vicky-1) (FITC conjugate) at a concentration of 50ug/ml.](http://images.novusbio.com/fullsize/BCMA-TNFRSF17-Antibody-Vicky-1-Flow-Cytometry-NBP1-97637-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: Bax Antibody [NBP2-67285] - Staining Bax in F9 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/Bax-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-67285-img0007.jpg "Immunocytochemistry/Immunofluorescence: Bax Antibody [NBP2-67285] - Staining Bax in F9 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.")
![Immunohistochemistry-Paraffin: Bax Antibody [NBP2-67285] - Analysis of paraffin-embedded mouse testis tissue using anti-Bax antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Bax-Antibody-Immunohistochemistry-Paraffin-NBP2-67285-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: Bax Antibody [NBP2-67285] - Staining Bax in HepG2 cells (green). The nuclear counter stain is DAPI (blue).Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/Bax-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-67285-img0002.jpg)
![Immunohistochemistry-Paraffin: Bax Antibody [NBP2-67285] - Analysis of paraffin-embedded human cervical tissue using anti-Bax antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Bax-Antibody-Immunohistochemistry-Paraffin-NBP2-67285-img0003.jpg)
![Immunohistochemistry-Paraffin: Bax Antibody [NBP2-67285] - Analysis of paraffin-embedded human gall bladder tissue using anti-Bax antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Bax-Antibody-Immunohistochemistry-Paraffin-NBP2-67285-img0004.jpg)
![Western Blot: Bax Antibody [NBP2-67285] - Analysis of BAX on different lysates with Rabbit anti-BAX antibody at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution.Lane 1: HeLa cell lysateLane 2: MCF7 cell lysateLane 3: HEK-293 cell lysateLysates/proteins at 15 ug/Lane.Predicted band size: 21 kDaObserved band size: 21 kDaExposure time: 1 minute 34 seconds; ECL: K1801;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 at 1/5,000 dilution and competitor's antibody at 1/1,000 dilution were used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp2-67285_rabbit-monoclonal-bax-antibody-western-blot-1872024115652..jpg)
![Immunocytochemistry/Immunofluorescence: Bax Antibody [NBP2-67285] - Analysis of SHSY5Y cells labeling BAX with Rabbit anti-BAX antibody at 1/200 dilution.Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-BAX antibody at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488,) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.Beta Ⅲ tubulin ( red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 647, were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp2-67285_rabbit-monoclonal-bax-antibody-immunocytochemistry-immunofluorescence-1872024115923..jpg)
![Immunocytochemistry/Immunofluorescence: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Staining CD147 in SKOV-3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100/PBS.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunocytochemistry-Immunofluorescence-NBP2-66820-img0003.jpg "Immunocytochemistry/Immunofluorescence: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Staining CD147 in SKOV-3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100/PBS.")
![Immunohistochemistry-Paraffin: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Analysis of paraffin-embedded rat brain tissue using anti-CD147 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunohistochemistry-Paraffin-NBP2-66820-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Staining CD147 in A431 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100/PBS.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunocytochemistry-Immunofluorescence-NBP2-66820-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Staining CD147 in HeLa cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X-100/PBS.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunocytochemistry-Immunofluorescence-NBP2-66820-img0002.jpg)
![Immunohistochemistry-Paraffin: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Analysis of paraffin-embedded human colon cancer tissue using anti-CD147 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunohistochemistry-Paraffin-NBP2-66820-img0004.jpg)
![Immunohistochemistry-Paraffin: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Analysis of paraffin-embedded mouse brain tissue using anti-CD147 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunohistochemistry-Paraffin-NBP2-66820-img0005.jpg)
![Immunohistochemistry-Paraffin: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Analysis of paraffin-embedded mouse heart tissue using anti-CD147 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunohistochemistry-Paraffin-NBP2-66820-img0006.jpg)
![Immunohistochemistry-Paraffin: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - Analysis of paraffin-embedded mouse testis tissue using anti-CD147 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/EMMPRIN-CD147-Antibody-JF1-045-Immunohistochemistry-Paraffin-NBP2-66820-img0007.jpg)
![Western Blot: EMMPRIN/CD147 Antibody (JF1-045) [NBP2-66820] - analysis of CD147 on different lysates with Rabbit anti-CD147 antibody at 1/5,000 dilution.Lane 1: HepG2 cell lysate (15 ug/Lane)Lane 2: NCI-H226 cell lysate (15 ug/Lane)Lane 3: 786-0 cell lysate (15 µg/Lane)Lane 4: RAW264.7 cell lysate (15 ug/Lane)Lane 5: Mouse liver tissue lysate (20 ug/Lane)Lane 6: Rat liver tissue lysate (20 ug/Lane)Predicted band size: 42 kDaObserved band size: 45-60 kDaExposure 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 (at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp2-66820_rabbit-monoclonal-emmprin-cd147-antibody-jf1-045-western-blot-187202410416..jpg)
![Immunohistochemistry: HLA G Antibody (MEM-G/1) [NB500-302] - ELA affects first trimester placental explant trophoblast proliferation. HLA-G immunostaining (brown color) indicates the location of extravillous trophoblasts. In control explants (left panel) almost all villous cytotrophoblasts proliferate, while this is much less apparent in explants treated with ELA (0.25nM, right panel). Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/s41598-019-55650-5) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/HLA-G-Antibody-MEM-G-1-Immunohistochemistry-NB500-302-img0005.jpg "Immunohistochemistry: HLA G Antibody (MEM-G/1) [NB500-302] - ELA affects first trimester placental explant trophoblast proliferation. HLA-G immunostaining (brown color) indicates the location of extravillous trophoblasts. In control explants (left panel) almost all villous cytotrophoblasts proliferate, while this is much less apparent in explants treated with ELA (0.25nM, right panel). Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/s41598-019-55650-5) licensed under a CC-BY license.")
![Western Blot: HLA G Antibody (MEM-G/1) [NB500-302] - Using the Biotin direct conjugate analysis (reducing conditions) of HLA-G1 in HLA-G1 transfectants using the antibody MEM-G/1 biotin.](http://images.novusbio.com/fullsize/HLA-G-Antibody-MEM-G-1-Western-Blot-NB500-302-img0003.jpg)
![Immunohistochemistry: HLA G Antibody (MEM-G/1) [NB500-302] - Fig. 1B - first-trimester placenta (paraffin-embedded sections)](http://images.novusbio.com/fullsize/HLA-G-Antibody-MEM-G-1-Immunohistochemistry-NB500-302-img0001.jpg)
![Immunohistochemistry: HLA G Antibody (MEM-G/1) [NB500-302] - Fig. 1. Immunohistochemistry staining with anti-human HLA-G (MEM-G/1). Fig. 1A - pulmonary disseases (paraffin-embedded sections) The antibody MEM-G/1 stains infiltrating macrophages in pulmonary diseases. In the top left corner see the detail of macrophage.](http://images.novusbio.com/fullsize/HLA-G-Antibody-MEM-G-1-Immunohistochemistry-NB500-302-img0002.jpg)
![Immunohistochemistry: HLA G Antibody (MEM-G/1) - BSA Free [NB500-302] - ELA affects first trimester placental explant trophoblast proliferation. (a) HLA-G immunostaining (brown color top panel) indicates the location of extravillous trophoblasts. PhosphoH3(Ser10) immunostaining (brown color lower 3 panels) identifies proliferating cells undergoing mitosis. In extravillous trophoblasts of explants treated with ELA proliferation appears to decrease. In control explants almost all villous cytotrophoblasts proliferate, while this is much less apparent in explants treated with ELA. Treatment with ELA in combination with ML221 does not return villous cytotrophoblast proliferation to the level as seen in control explants. (b) Quantifying the percentage of proliferating extravillous trophoblasts observed by immunohistochemistry shows a significant decrease upon treatment with ELA which cannot be rescued by the addition of ML221. P = 0.08 between controls & explants treated with ELA & ML221. n = 12 placentas, 5 explants per treatment. Bars represent mean ± SEM & data was tested with one-way ANOVA followed by Bonferroni multiple comparisons test. *Indicates p < 0.05. (c) Treatment of explants with an ELA neutralizing antibody shows a significant increase of extravillous trophoblast proliferation upon quantifying immunohistochemistry stainings. n = 4 placentas, 5 explants per treatment. Bars represent mean ± SEM & data was tested with a Student’s t-test. *Indicates p < 0.05. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31836787), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb500-302_mouse-monoclonal-hla-g-antibody-mem-g-1-31020241617149.jpg)