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![Immunohistochemistry-Paraffin: KCNN4 Antibody [NBP3-14383] - Immunohistochemistry of formalin-fixed, paraffin-embedded human prostate after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/KCNN4 Antibody-Immunohistochemistry-Paraffin-NBP3-14383-img0001.jpg "Immunohistochemistry-Paraffin: KCNN4 Antibody [NBP3-14383] - Immunohistochemistry of formalin-fixed, paraffin-embedded human prostate after heat-induced antigen retrieval.")
![Western Blot: CXXC1 Antibody [NBP2-84741] - WB Suggested Anti-Cxxc1 Antibody. Titration: 1.0 ug/ml. Positive Control: Rat Testis](http://images.novusbio.com/fullsize/CXXC1-Antibody-Western-Blot-NBP2-84741-img0001.jpg "Western Blot: CXXC1 Antibody [NBP2-84741] - WB Suggested Anti-Cxxc1 Antibody. Titration: 1.0 ug/ml. Positive Control: Rat Testis")
![Western Blot: Myt1 Antibody [NBP2-87874] - WB Suggested Anti-Myt1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Mouse Uterus](http://images.novusbio.com/fullsize/Myt1-Antibody-Western-Blot-NBP2-87874-img0001.jpg "Western Blot: Myt1 Antibody [NBP2-87874] - WB Suggested Anti-Myt1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Mouse Uterus")
![Immunohistochemistry: p53 Antibody (PD01-32) [NBP3-32699] - Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue with Rabbit anti-p53 antibody (NBP3-32699) at 1/2,000 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 (NBP3-32699) at 1/2,000 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/nbp3-32699_rabbit-p53-mab-pd01-32-298202413585511.jpg "Immunohistochemistry: p53 Antibody (PD01-32) [NBP3-32699] - Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue with Rabbit anti-p53 antibody (NBP3-32699) at 1/2,000 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 (NBP3-32699) at 1/2,000 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.")
![Western Blot: CXXC1 Antibody [NBP2-84740] - WB Suggested Anti-CXXC1 Antibody Titration: 0.625ug/ml. ELISA Titer: 1:62500. Positive Control: Transfected 293T](http://images.novusbio.com/fullsize/CXXC1-Antibody-Western-Blot-NBP2-84740-img0001.jpg "Western Blot: CXXC1 Antibody [NBP2-84740] - WB Suggested Anti-CXXC1 Antibody Titration: 0.625ug/ml. ELISA Titer: 1:62500. Positive Control: Transfected 293T")
![Western Blot: PHF21A Antibody [NBP2-99586] - Anti-PHF21A rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: Jurkat Whole Cell Lysate Lane C: HT1080 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 75 kDa](http://images.novusbio.com/fullsize/PHF21A-Antibody-Western-Blot-NBP2-99586-img0002.jpg "Western Blot: PHF21A Antibody [NBP2-99586] - Anti-PHF21A rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa Whole Cell Lysate Lane B: Jurkat Whole Cell Lysate Lane C: HT1080 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 75 kDa")
![Immunohistochemistry: Stathmin 1 Antibody (PD00-54) [NBP3-32981] - Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Stathmin 1 antibody (NBP3-32981) at 1/2,000 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 (NBP3-32981) at 1/2,000 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/nbp3-32981_rabbit-stathmin-1-mab-pd00-54-29820241435219.jpg "Immunohistochemistry: Stathmin 1 Antibody (PD00-54) [NBP3-32981] - Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-Stathmin 1 antibody (NBP3-32981) at 1/2,000 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 (NBP3-32981) at 1/2,000 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.")
![Immunocytochemistry/Immunofluorescence: GADD153/CHOP Antibody [NBP2-98741] - Immunofluorescence staining of GADD153/CHOP in Hela cells. Cells were fixed with 4% PFA, blocked with 10% serum. Then incubated with NBP2-98741 antibody (1:1000)(Figure A), incubated with NBP2-98741 antibody and antigen (Figure B) 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 nucleus.](http://images.novusbio.com/fullsize/nbp2-98741_rabbit-polyclonal-gadd153-chop-antibody-23520251129390.png "Immunocytochemistry/Immunofluorescence: GADD153/CHOP Antibody [NBP2-98741] - Immunofluorescence staining of GADD153/CHOP in Hela cells. Cells were fixed with 4% PFA, blocked with 10% serum. Then incubated with NBP2-98741 antibody (1:1000)(Figure A), incubated with NBP2-98741 antibody and antigen (Figure B) 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 nucleus.")
![Western Blot: PHF21A Antibody [NBP2-88045] - WB Suggested Anti-PHF21A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Jurkat cell lysate](http://images.novusbio.com/fullsize/PHF21A-Antibody-Western-Blot-NBP2-88045-img0001.jpg "Western Blot: PHF21A Antibody [NBP2-88045] - WB Suggested Anti-PHF21A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Jurkat cell lysate")
![Immunohistochemistry-Paraffin: USP19 Antibody [NBP3-14512] - Human Brain, Cortex: Formalin-Fixed, Paraffin-Embedded (FFPE)](http://images.novusbio.com/fullsize/USP19 Antibody-Immunohistochemistry-Paraffin-NBP3-14512-img0001.jpg "Immunohistochemistry-Paraffin: USP19 Antibody [NBP3-14512] - Human Brain, Cortex: Formalin-Fixed, Paraffin-Embedded (FFPE)")
![Chromatin Immunoprecipitation: KAT3B/p300 Antibody (1H11G2) [NBP2-59233] - ChIP was performed using HeLa cells, the antibody against p300 and optimized PCR primer sets for qPCR. ChIP was performed with a ChIP-seq kit, using sheared chromatin from 4 million cells. A titration of the antibody consisting of 1, 2, 5 and 10 ug per ChIP experiment was analysed. IgG (2 ug/IP) was used as negative IP control. Quantitative PCR was performed with primers for two genomic regions near the ANKRD32 and IRS2 genes, used as positive controls, and for the coding region of the inactive MYOD1 gene and an intergeic region on chromosome 11, used as negative controls. Figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).](http://images.novusbio.com/fullsize/KAT3B-p300-Antibody-1H11G2-Chromatin-Immunoprecipitation-NBP2-59233-img0001.jpg "Chromatin Immunoprecipitation: KAT3B/p300 Antibody (1H11G2) [NBP2-59233] - ChIP was performed using HeLa cells, the antibody against p300 and optimized PCR primer sets for qPCR. ChIP was performed with a ChIP-seq kit, using sheared chromatin from 4 million cells. A titration of the antibody consisting of 1, 2, 5 and 10 ug per ChIP experiment was analysed. IgG (2 ug/IP) was used as negative IP control. Quantitative PCR was performed with primers for two genomic regions near the ANKRD32 and IRS2 genes, used as positive controls, and for the coding region of the inactive MYOD1 gene and an intergeic region on chromosome 11, used as negative controls. Figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).")
![SDS-Page: Recombinant Human NT-proBNP Protein [NBP2-61321] - Recombinant Human NT-proBNP Protein.](http://images.novusbio.com/fullsize/Recombinant-Human-proBNP-Protein-SDS-Page-NBP2-61321-img0002.jpg "SDS-Page: Recombinant Human NT-proBNP Protein [NBP2-61321] - Recombinant Human NT-proBNP Protein.")