| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35292-10ug | |||
| Carrier-Free | NBP2-35292-1mg | |||
| Carrier-Free | NBP2-35292-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20130-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26396-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26388-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26240-50ul | |||
![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).")
![SDS-Page: Rat Cardiotrophin-1/CT-1 Protein [NBP2-35292]](http://images.novusbio.com/fullsize/Rat-Cardiotrophin-1-CT-1-Protein-SDS-Page-NBP2-35292-img0001.jpg "SDS-Page: Rat Cardiotrophin-1/CT-1 Protein [NBP2-35292]")
![Immunocytochemistry/Immunofluorescence: Geminin Antibody (8H8) [NBP3-15158] - Immunofluorescence staining of Hela Cells with at Geminin antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-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/Geminin-Antibody-8H8-Immunocytochemistry-Immunofluorescence-NBP3-15158-img0001.jpg "Immunocytochemistry/Immunofluorescence: Geminin Antibody (8H8) [NBP3-15158] - Immunofluorescence staining of Hela Cells with at Geminin antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-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).")
![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).")
![Western Blot: Thymidylate Synthase Antibody (2B2) [NBP3-15154] - Positive WB detected in: Hela whole cell lysate, 293T whole cell lysate, 293 whole cell lysate, Jurkat whole cell lysate, HepG2 whole cell lysate, HL-60 whole cell lysate. All lanes: Thymidylate Synthase antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 36, 32, 27 KDa. Observed band size: 36 KDa.](http://images.novusbio.com/fullsize/Thymidylate-Synthase-Antibody-2B2-Western-Blot-NBP3-15154-img0001.jpg "Western Blot: Thymidylate Synthase Antibody (2B2) [NBP3-15154] - Positive WB detected in: Hela whole cell lysate, 293T whole cell lysate, 293 whole cell lysate, Jurkat whole cell lysate, HepG2 whole cell lysate, HL-60 whole cell lysate. All lanes: Thymidylate Synthase antibody at 1:2000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 36, 32, 27 KDa. Observed band size: 36 KDa.")
![Western Blot: SMC1 [p Ser957] Antibody (1F9) [NBP3-26388] - Positive Western Blot detected in 293 whole cell lysate (treated with Calyculin A or not). All lanes: SMC1 [p Ser957] Antibody at 1.11ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 160 KDa Observed band size: 160 KDa](http://images.novusbio.com/fullsize/nbp3-26388_rabbit-smc1-p-ser-957-mab-1f9-282202411485814.jpg "Western Blot: SMC1 [p Ser957] Antibody (1F9) [NBP3-26388] - Positive Western Blot detected in 293 whole cell lysate (treated with Calyculin A or not). All lanes: SMC1 [p Ser957] Antibody at 1.11ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 160 KDa Observed band size: 160 KDa")
![Western Blot: HDAC1 Antibody (10A1) [NBP3-26240] - Positive Western Blot detected in: Hela whole cell lysate, K562 whole cell lysate, Jurkat whole cell lysate, HL60 whole cell lysate. All lanes: HDAC1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 56 kDa Observed band size: 60 kDa](http://images.novusbio.com/fullsize/nbp3-26240_rabbit-hdac1-mab-10a1-282202411485840.jpg "Western Blot: HDAC1 Antibody (10A1) [NBP3-26240] - Positive Western Blot detected in: Hela whole cell lysate, K562 whole cell lysate, Jurkat whole cell lysate, HL60 whole cell lysate. All lanes: HDAC1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 56 kDa Observed band size: 60 kDa")