| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-23507-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-34911-1mg | |||
| Carrier-Free | NBP2-34911-100ug | |||
| Carrier-Free | NBP2-34911-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35036-1mg | |||
| Carrier-Free | NBP2-35036-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35102-10ug | |||
| Carrier-Free | NBP2-35102-1mg | |||
| Carrier-Free | NBP2-35102-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81111-0.025mg | |||
![Immunohistochemistry-Paraffin: p38 alpha Antibody (0004) [NBP3-23507] - Immunohistochemical analysis of paraffin-embedded human carcinoma of sigmoid tissue,untreated (left) or lambda phosphatase-treated (right), using NBP3-23507 at 1:500 dilution.](http://images.novusbio.com/fullsize/nbp3-23507_rabbit-p38-alpha-mab-0004-235202511444436.png "Immunohistochemistry-Paraffin: p38 alpha Antibody (0004) [NBP3-23507] - Immunohistochemical analysis of paraffin-embedded human carcinoma of sigmoid tissue,untreated (left) or lambda phosphatase-treated (right), using NBP3-23507 at 1:500 dilution.")
![Western Blot: Cholecystokinin-B R/CCKBR Antibody [NBP2-88785] - Host: Rabbit. Target Name: CCKBR. Sample Tissue: Human MCF7 Whole Cell lysates. Antibody Dilution: 1ug/ml](http://images.novusbio.com/fullsize/Cholecystokinin-B-R-CCKBR-Antibody-Western-Blot-NBP2-88785-img0001.jpg "Western Blot: Cholecystokinin-B R/CCKBR Antibody [NBP2-88785] - Host: Rabbit. Target Name: CCKBR. Sample Tissue: Human MCF7 Whole Cell lysates. Antibody Dilution: 1ug/ml")
![Western Blot: EGFR [p Tyr845] Antibody (JE46-77) [NBP3-32761] - Western blot analysis of EGFR on different lysates with Rabbit anti-EGFR antibody (NBP3-32761) at 1/1,000 dilution. Lane 1: A431 whole cell lysate Lane 2: A431 treated with 100ng/mL EGF for 10 minutes whole cell lysate Lane 3: A431 whole cell lysate treated with pp for 1 hour Lane 4: A431 treated with 100ng/mL EGF for 10 minutes whole cell lysate treated with pp for 1 hour Lysates/proteins at 20 ug/Lane. Predicted band size: 134 kDa Observed band size: 180/75 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32761) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32761_rabbit-egfr-p-tyr845-mab-je46-77-28820241244290.jpg "Western Blot: EGFR [p Tyr845] Antibody (JE46-77) [NBP3-32761] - Western blot analysis of EGFR on different lysates with Rabbit anti-EGFR antibody (NBP3-32761) at 1/1,000 dilution. Lane 1: A431 whole cell lysate Lane 2: A431 treated with 100ng/mL EGF for 10 minutes whole cell lysate Lane 3: A431 whole cell lysate treated with pp for 1 hour Lane 4: A431 treated with 100ng/mL EGF for 10 minutes whole cell lysate treated with pp for 1 hour Lysates/proteins at 20 ug/Lane. Predicted band size: 134 kDa Observed band size: 180/75 kDa Exposure time: 3 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32761) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Western Blot: Cholecystokinin-B R/CCKBR Antibody [NBP2-88784] - WB Suggested Anti-CCKBR Antibody. Titration: 1.0 ug/ml. Positive Control: Placenta](http://images.novusbio.com/fullsize/Cholecystokinin-B-R-CCKBR-Antibody-Western-Blot-NBP2-88784-img0001.jpg "Western Blot: Cholecystokinin-B R/CCKBR Antibody [NBP2-88784] - WB Suggested Anti-CCKBR Antibody. Titration: 1.0 ug/ml. Positive Control: Placenta")
![Immunohistochemistry: ER alpha/NR3A1 Antibody (PD00-04) [NBP3-32321] - Immunohistochemical analysis of paraffin-embedded human cervix tissue with Rabbit anti-ER alpha/NR3A1 antibody (NBP3-32321) at 1/1,000 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 (NBP3-32321) 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/nbp3-32321_rabbit-er-alpha-nr3a1-mab-pd00-04-298202413585568.jpg "Immunohistochemistry: ER alpha/NR3A1 Antibody (PD00-04) [NBP3-32321] - Immunohistochemical analysis of paraffin-embedded human cervix tissue with Rabbit anti-ER alpha/NR3A1 antibody (NBP3-32321) at 1/1,000 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 (NBP3-32321) 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.")
![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).")
![Immunohistochemistry-Paraffin: Estrogen Receptor Antibody (S21-V) [NBP1-30153] - human of breast tumor tissue stained with Estrogen Receptor antibody shows strong positive nuclear immunostaining.](http://images.novusbio.com/fullsize/108721_1.jpg "Immunohistochemistry-Paraffin: Estrogen Receptor Antibody (S21-V) [NBP1-30153] - human of breast tumor tissue stained with Estrogen Receptor antibody shows strong positive nuclear immunostaining.")
![Western Blot: Fibrin beta-chain Antibody (59D8) - BSA Free [NBP3-43554] - Human liver (A), placenta (B), and serum (C) tissue lysates (35µg protein in RIPA buffer) were resolved via SDS-PAGE, and the subsequent blots were probed with NBP3-43554 at 0.01µg/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp3-43554_mouse-fibrin-beta-chain-mab-59d8-azide-and-bsa-free-western-blot-2220260351115.png "Western Blot: Fibrin beta-chain Antibody (59D8) - BSA Free [NBP3-43554] - Human liver (A), placenta (B), and serum (C) tissue lysates (35µg protein in RIPA buffer) were resolved via SDS-PAGE, and the subsequent blots were probed with NBP3-43554 at 0.01µg/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.")
![Immunocytochemistry/ Immunofluorescence: Fibrin beta-chain Antibody (59D8) - BSA Free [NBP3-43554] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on coverslips stained with NBP3-43554 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43554, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-48432_rabbit-vaccinia-virus-b18r-pab-azide-and-bsa-free-western-blot-2220260311813.png)
![SDS-Page: Human CXCL10/IP-10/CRG-2 Protein [NBP2-34911]](http://images.novusbio.com/fullsize/Human-CXCL10-IP-10-CRG-2-Protein-SDS-Page-NBP2-34911-img0001.jpg "SDS-Page: Human CXCL10/IP-10/CRG-2 Protein [NBP2-34911]")
![SDS-Page: Mouse FGF-9 Protein [NBP2-35036]](http://images.novusbio.com/fullsize/Mouse-FGF-9-Protein-SDS-Page-NBP2-35036-img0001.jpg "SDS-Page: Mouse FGF-9 Protein [NBP2-35036]")
![SDS-Page: Mouse IL-11 Protein [NBP2-35102]](http://images.novusbio.com/fullsize/Mouse-IL-11-Protein-SDS-Page-NBP2-35102-img0001.jpg "SDS-Page: Mouse IL-11 Protein [NBP2-35102]")
![Flow Cytometry: Fibrin beta-chain Antibody (8E5) - Chimeric [NBP2-81111] - Flow-cytometry using the Fibrin beta-chain Antibody [NBP2-81111]. HepG2 cells were fixed using 2% PFA, permeabilised using 0.5% Triton and stained with anti-Fluorescein IgG antibody (isotype control, black line) or the rabbit IgG-chimeric version of 8E5 (NBP2-81111, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Fibrinopeptide-B-Antibody-8E5-Chimeric-Flow-Cytometry-NBP2-81111-img0001.jpg "Flow Cytometry: Fibrin beta-chain Antibody (8E5) - Chimeric [NBP2-81111] - Flow-cytometry using the Fibrin beta-chain Antibody [NBP2-81111]. HepG2 cells were fixed using 2% PFA, permeabilised using 0.5% Triton and stained with anti-Fluorescein IgG antibody (isotype control, black line) or the rabbit IgG-chimeric version of 8E5 (NBP2-81111, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.")