| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99421-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-99646-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-2660-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-54807-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50606-0.025ml | |||
![Western Blot: NF2/Merlin Antibody [NBP2-99421] - Anti-NF2/Merlin rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa 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: 69 kDa. Observed band size: 69 kDa (We are unsure as to the identity of these extra bands).](http://images.novusbio.com/fullsize/NF2-Merlin-Antibody-Western-Blot-NBP2-99421-img0002.jpg "Western Blot: NF2/Merlin Antibody [NBP2-99421] - Anti-NF2/Merlin rabbit polyclonal antibody at 1:500 dilution. Lane A: HeLa 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: 69 kDa. Observed band size: 69 kDa (We are unsure as to the identity of these extra bands).")
![Western Blot: UbcH7/UBE2L3 Antibody [NBP2-99646] - Anti-UbcH7/UBE2L3 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat 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: 18 kDa. Observed band size: 18 kDa](http://images.novusbio.com/fullsize/UbcH7-UBE2L3-Antibody-Western-Blot-NBP2-99646-img0002.jpg "Western Blot: UbcH7/UBE2L3 Antibody [NBP2-99646] - Anti-UbcH7/UBE2L3 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat 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: 18 kDa. Observed band size: 18 kDa")
![Western Blot: TRADD Antibody [NBP3-10286] - Western blot analysis using NBP3-10286 on Human DU145 as a positive control. Antibody Titration: 0.2-1 ug/ml](http://images.novusbio.com/fullsize/TRADD-Antibody-Western-Blot-NBP3-10286-img0001.jpg "Western Blot: TRADD Antibody [NBP3-10286] - Western blot analysis using NBP3-10286 on Human DU145 as a positive control. Antibody Titration: 0.2-1 ug/ml")
![Immunohistochemistry: Bax Antibody (PD01-44) [NBP3-32070] - Immunohistochemical analysis of paraffin-embedded human breast tissue with Rabbit anti-Bax antibody (NBP3-32070) at 1/200 dilution.<br/><br/> 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 (NBP3-32070) at 1/200 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/nbp3-32070_rabbit-bax-mab-pd01-44-298202414333653.jpg "Immunohistochemistry: Bax Antibody (PD01-44) [NBP3-32070] - Immunohistochemical analysis of paraffin-embedded human breast tissue with Rabbit anti-Bax antibody (NBP3-32070) at 1/200 dilution.<br/><br/> 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 (NBP3-32070) at 1/200 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.")
![ELISA: Human ATG16L1 Â - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-31133] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-31133_human-atg16l1-ready-to-use-elisa-kit-colorimetric-206202415314851.png "ELISA: Human ATG16L1 Â - Ready-To-Use ELISA Kit (Colorimetric) [NBP3-31133] - Standard Curve Reference")
![Immunohistochemistry-Paraffin: SLC5A3 Antibody - BSA Free [NB110-40431] - Analysis of SLC5A3 Antibody with human spinal cord at concentration 20 ug/ml.](http://images.novusbio.com/fullsize/SLC5A3-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NB110-40431-img0001.jpg "Immunohistochemistry-Paraffin: SLC5A3 Antibody - BSA Free [NB110-40431] - Analysis of SLC5A3 Antibody with human spinal cord at concentration 20 ug/ml.")
![Immunohistochemistry: CD34 Antibody (PDM0-12) [NBP3-32148] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-CD34 antibody (NBP3-32148) at 1/1,000 dilution.<br/><br/> 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 (NBP3-32148) 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/nbp3-32148_mouse-cd34-mab-pdm0-12-29820241426264.jpg "Immunohistochemistry: CD34 Antibody (PDM0-12) [NBP3-32148] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-CD34 antibody (NBP3-32148) at 1/1,000 dilution.<br/><br/> 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 (NBP3-32148) 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.")
![Western Blot: RBBP4/RbAp48 Antibody (C.15200033) [NBP2-62798] - Analysis of nuclear extracts from HeLa cells (20 ug) using the monoclonal antibody against hRbAp46/48.](http://images.novusbio.com/fullsize/RBBP4-RbAp48-Antibody-C-15200033-Western-Blot-NBP2-62798-img0001.jpg "Western Blot: RBBP4/RbAp48 Antibody (C.15200033) [NBP2-62798] - Analysis of nuclear extracts from HeLa cells (20 ug) using the monoclonal antibody against hRbAp46/48.")
![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).")
![Western Blot: AIF Antibody (3C11) [NBP2-50606] - Western blot was performed on transfected 293T cell lysates using anti-AIF [3C11].](http://images.novusbio.com/fullsize/AIF-Antibody-3C11-Western-Blot-NBP2-50606-img0001.jpg "Western Blot: AIF Antibody (3C11) [NBP2-50606] - Western blot was performed on transfected 293T cell lysates using anti-AIF [3C11].")