| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20130-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-2660-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50606-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26396-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26487-50ul | |||
![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).")
![ELISA: RRM1 Antibody (4E4) [H00006240-M03] - Detection limit for recombinant GST tagged RRM1 is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/RRM1-Antibody-4E4-ELISA-H00006240-M03-img0001.jpg "ELISA: RRM1 Antibody (4E4) [H00006240-M03] - Detection limit for recombinant GST tagged RRM1 is approximately 0.3ng/ml as a capture antibody.")
![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].")
![Western Blot: AIF [p Ser116] Antibody [NBP3-23346] - Western blot image of human jurkat cells untreated (lanes 1 & 3) or treated with calyculin A (100 nM, 30 min.) (lanes 2 and 4). The blot was probed with rabbit polyclonals anti-AIF (C-terminal region) at 1:500 (lanes 1 & 2) and anti-AIF (Ser-116) phospho-specific antibody at 1:1000 (lanes 3 & 4).](http://images.novusbio.com/fullsize/nbp3-23346_rabbit-aif-p-ser116-pab-1992023191546.jpg "Western Blot: AIF [p Ser116] Antibody [NBP3-23346] - Western blot image of human jurkat cells untreated (lanes 1 & 3) or treated with calyculin A (100 nM, 30 min.) (lanes 2 and 4). The blot was probed with rabbit polyclonals anti-AIF (C-terminal region) at 1:500 (lanes 1 & 2) and anti-AIF (Ser-116) phospho-specific antibody at 1:1000 (lanes 3 & 4).")
![Immunocytochemistry/Immunofluorescence: RPA2 [p Thr21] Antibody (3B2) [NBP3-26396] - Staining of Hela cells with RPA2 [p Thr21] Antibody (3B2) at 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 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26396_rabbit-rpa2-p-thr-21-mab-3b2-282202412493635.jpg "Immunocytochemistry/Immunofluorescence: RPA2 [p Thr21] Antibody (3B2) [NBP3-26396] - Staining of Hela cells with RPA2 [p Thr21] Antibody (3B2) at 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 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).")
![Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26487_rabbit-aurora-a-mab-1h8-282202412493636.jpg "Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).")