| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-70610 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-92408-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-92331-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-93090-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-04987-20ul | |||
![Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with SESN1 antibody [HL1750] (NBP3-48662) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-48662_rabbit-sesn1-mab-hl1750-western-blot-141120251826019.jpg "<b>Genetic Strategies Validation. </b>Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with SESN1 antibody [HL1750] (NBP3-48662) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![Western Blot: p53 [p Ser6] Antibody [NBP3-13310] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with p53 (phospho Ser6) antibody (NBP3-13310) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/p53-[p-Ser6]-Antibody-Western-Blot-NBP3-13310-img0002.jpg "<b>Biological Strategies Validation. </b>Western Blot: p53 [p Ser6] Antibody [NBP3-13310] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with p53 (phospho Ser6) antibody (NBP3-13310) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Biological Strategies Validation. </b>Western Blot: p53 [p Ser6] Antibody [NBP3-13310] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with p53 (phospho Ser6) antibody (NBP3-13310) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/p53-[p-Ser6]-Antibody-Western-Blot-NBP3-13310-img0001.jpg)
![Western Blot: DUSP4 Antibody (OTI7C11) [NBP2-46479] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY DUSP4 ( 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 antiDUSP4.(1:2000)](http://images.novusbio.com/fullsize/DUSP4-Antibody-OTI7C11-Western-Blot-NBP2-46479-img0002.jpg "Western Blot: DUSP4 Antibody (OTI7C11) [NBP2-46479] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY DUSP4 ( 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 antiDUSP4.(1:2000)")
![Immunocytochemistry/Immunofluorescence: ZMYND11 Antibody [NB100-1157] - Paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary antibody incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nuclear staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/ZMYND11-Antibody-Immunocytochemistry-Immunofluorescence-NB100-1157-img0001.jpg "Immunocytochemistry/Immunofluorescence: ZMYND11 Antibody [NB100-1157] - Paraformaldehyde fixed U2OS cells, permeabilized with 0.15% Triton. Primary antibody incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nuclear staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10ug/ml) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).")
![Western Blot: MAD2L1-binding protein Antibody [NBP1-79887] - Titration: 2 ug/ml Positive Control: A549 lung cancer cells.](http://images.novusbio.com/fullsize/MAD2L1-binding-protein-Antibody-Western-Blot-NBP1-79887-img0003.jpg "Western Blot: MAD2L1-binding protein Antibody [NBP1-79887] - Titration: 2 ug/ml Positive Control: A549 lung cancer cells.")
![Western Blot: MAD2L1-binding protein Antibody [NBP1-79887] - Titration: 1.0 ug/ml Positive Control: MDA-MB-435S Whole Cell.](http://images.novusbio.com/fullsize/MAD2L1-binding-protein-Antibody-Western-Blot-NBP1-79887-img0002.jpg)
![Western Blot: FRA-1/FOSL1 Antibody [NB100-40803] - (1ug/ml) staining of Human Bone Marrow lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/FRA-1-FOSL1-Antibody-Western-Blot-NB100-40803-img0003.jpg "Western Blot: FRA-1/FOSL1 Antibody [NB100-40803] - (1ug/ml) staining of Human Bone Marrow lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Western Blot: Cyclin G2 Antibody [NBP1-79935] - Sample Tissue: Human 293T Antibody Dilution: 1.0 ug/ml](http://images.novusbio.com/fullsize/Cyclin-G2-Antibody-Western-Blot-NBP1-79935-img0003.jpg "Western Blot: Cyclin G2 Antibody [NBP1-79935] - Sample Tissue: Human 293T Antibody Dilution: 1.0 ug/ml")
![Western Blot: Cyclin G2 Antibody [NBP1-79935] - Jurkat Cell Lysate 2.5ug/ml; Gel Concentration: 12%](http://images.novusbio.com/fullsize/Cyclin-G2-Antibody-Western-Blot-NBP1-79935-img0002.jpg)
![Western Blot: TRF-1 Antibody [NB100-891] - Analysis of TRF1 in HeLa lysate (RIPA buffer, 30ug total protein per lane) using this antibody at 2 ug/ml. Primary incubated for 12 hour. Detected using chemiluminescence.](http://images.novusbio.com/fullsize/TRF-1-Antibody-Western-Blot-NB100-891-img0004.jpg "Western Blot: TRF-1 Antibody [NB100-891] - Analysis of TRF1 in HeLa lysate (RIPA buffer, 30ug total protein per lane) using this antibody at 2 ug/ml. Primary incubated for 12 hour. Detected using chemiluminescence.")
![Western Blot: BRD7 Antibody [NBP2-92408] - Western blot analysis of extracts from normal (control) and BRD7 Rabbit pAb knockout (KO) 293T cells, using BRD7 Rabbit pAb antibody (NBP2-92408) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.](http://images.novusbio.com/fullsize/BRD7-Antibody-Western-Blot-NBP2-92408-img0002.jpg "<b>Genetic Strategies Validation. </b>Western Blot: BRD7 Antibody [NBP2-92408] - Western blot analysis of extracts from normal (control) and BRD7 Rabbit pAb knockout (KO) 293T cells, using BRD7 Rabbit pAb antibody (NBP2-92408) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.")
![<b>Genetic Strategies Validation. </b>Western Blot: BRD7 Antibody [NBP2-92408] - Analysis of extracts of various cell lines, using BRD7 at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 60s.](http://images.novusbio.com/fullsize/BRD7-Antibody-Western-Blot-NBP2-92408-img0001.jpg)
![Western Blot: CDCA5 Antibody [NBP2-92331] - Analysis of extracts of various cell lines, using CDCA5 at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 1s.](http://images.novusbio.com/fullsize/CDCA5-Antibody-Western-Blot-NBP2-92331-img0001.jpg "Western Blot: CDCA5 Antibody [NBP2-92331] - Analysis of extracts of various cell lines, using CDCA5 at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 1s.")
![Western Blot: OAZ1 Antibody [NBP2-93090] - Analysis of extracts of various cell lines, using OAZ1 at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 60s.](http://images.novusbio.com/fullsize/OAZ1-Antibody-Western-Blot-NBP2-93090-img0002.jpg "Western Blot: OAZ1 Antibody [NBP2-93090] - Analysis of extracts of various cell lines, using OAZ1 at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 60s.")
![Western Blot: HERC5 Antibody [NBP3-04987] - Analysis of extracts of various cell lines, using HERC5 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit](http://images.novusbio.com/fullsize/HERC5-Antibody-Western-Blot-NBP3-04987-img0001.jpg "Western Blot: HERC5 Antibody [NBP3-04987] - Analysis of extracts of various cell lines, using HERC5 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit")