| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81075-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81039-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52647-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50533-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50532-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11966-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11502 | |||
![Flow Cytometry: Insulin R/CD220 Antibody (83-7) [NBP2-81039] - Flow-cytometry using the Insulin R/CD220 Antibody (83-7) [NBP2-81039]. Jurkat cells were stained with unimmunized rabbit IgG antibody (black line) or the rabbit-chimeric version of 83-7 (NBP2-81039, blue line) at a concentration of 10 ug/ml for 30 mins at RT. After washing, bound antibody was detected using anti-rabbit IgG JK (FITC-conjugate) antibody at 2 ug/ml and cells analyzed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Insulin-R-CD220-Antibody-83-7-Flow-Cytometry-NBP2-81039-img0001.jpg "Flow Cytometry: Insulin R/CD220 Antibody (83-7) [NBP2-81039] - Flow-cytometry using the Insulin R/CD220 Antibody (83-7) [NBP2-81039]. Jurkat cells were stained with unimmunized rabbit IgG antibody (black line) or the rabbit-chimeric version of 83-7 (NBP2-81039, blue line) at a concentration of 10 ug/ml for 30 mins at RT. After washing, bound antibody was detected using anti-rabbit IgG JK (FITC-conjugate) antibody at 2 ug/ml and cells analyzed on a FACSCanto flow-cytometer.")
![Flow Cytometry: CD38 Antibody (HB7) - Chimeric [NBP2-52647] - CD38 Antibody (HB7) [NBP2-52647] - Flow Cytometry using anti-CD38 antibody HB7. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HB7 (NBP2-52647, panel B) at a concentration of 1 ug/mL for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow cytometer.](http://images.novusbio.com/fullsize/CD38-Antibody-HB7-Chimeric-Flow-Cytometry-NBP2-52647-img0001.jpg "Flow Cytometry: CD38 Antibody (HB7) - Chimeric [NBP2-52647] - CD38 Antibody (HB7) [NBP2-52647] - Flow Cytometry using anti-CD38 antibody HB7. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HB7 (NBP2-52647, panel B) at a concentration of 1 ug/mL for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow cytometer.")
![In vitro assay: Recombinant Human alpha-Synuclein Active, Monomer, (Type 1) Acetyl (N-Term) Protein [NBP3-14768] - Thioflavin T assay for N-terminal acetylated alpha synuclein monomers (NBP3-14768) and pre-formed fibrils (PFFs) . Increased fluorescence, indicative of beta-sheet formation, was seen when 50 ug N-acetylated monomer and 5 ug N-acetylated fibril were combined, compared to monomer or fibril alone.](http://images.novusbio.com/fullsize/Recombinant-Human-alpha-Synuclein-Active-Monomer-Type-1-Acetyl-N-Term-Protein-In-vitro-assay-NBP3-14768-img0001.jpg "In vitro assay: Recombinant Human alpha-Synuclein Active, Monomer, (Type 1) Acetyl (N-Term) Protein [NBP3-14768] - Thioflavin T assay for N-terminal acetylated alpha synuclein monomers (NBP3-14768) and pre-formed fibrils (PFFs) . Increased fluorescence, indicative of beta-sheet formation, was seen when 50 ug N-acetylated monomer and 5 ug N-acetylated fibril were combined, compared to monomer or fibril alone.")
![Western Blot: Enolase 2/Neuron-specific Enolase Antibody (NSEP2) [NBP2-50533] - Lysates were separated on SDS-PAGE and probed with Anti-NSE [NSE-P2]. Lane 1: SH-SY5Y, Lane 2: NT2/D1.](http://images.novusbio.com/fullsize/Enolase-2-Neuron-specific-Enolase-Antibody-NSEP2-Western-Blot-NBP2-50533-img0001.jpg "Western Blot: Enolase 2/Neuron-specific Enolase Antibody (NSEP2) [NBP2-50533] - Lysates were separated on SDS-PAGE and probed with Anti-NSE [NSE-P2]. Lane 1: SH-SY5Y, Lane 2: NT2/D1.")
![Western Blot: Semaphorin 3A Antibody (M317) [NBP3-23375] - Western blots of human recombinant Semaphorin 3A/Fc chimera (95/125 kDa) (lanes 1-4). The blots were probed with rabbit polyclonal Semaphorin 3A (Central region) at 1:250 (lane 1) and 1:1000 (lane 2) and mouse monoclonal Semaphorin 3A (Central region) at 1:250 (lane 3) and 1:1000 (lane 4). Both antibodies recognize the 95 kDa and 125 kDa forms of the recombinant Semaphorin 3A.](http://images.novusbio.com/fullsize/nbp3-23375_mouse-semaphorin-3a-mab-m317-19920231856939.jpg "Western Blot: Semaphorin 3A Antibody (M317) [NBP3-23375] - Western blots of human recombinant Semaphorin 3A/Fc chimera (95/125 kDa) (lanes 1-4). The blots were probed with rabbit polyclonal Semaphorin 3A (Central region) at 1:250 (lane 1) and 1:1000 (lane 2) and mouse monoclonal Semaphorin 3A (Central region) at 1:250 (lane 3) and 1:1000 (lane 4). Both antibodies recognize the 95 kDa and 125 kDa forms of the recombinant Semaphorin 3A.")
![Western Blot: Enolase 2/Neuron-specific Enolase Antibody (NSEP1) [NBP2-50532] - Lysates were separated on SDS-PAGE and probed with Anti-NSE [NSE-P1]. Lane 1: SH-SY5Y, Lane 2: NT2/D1.](http://images.novusbio.com/fullsize/Enolase-2-Neuron-specific-Enolase-Antibody-NSEP1-Western-Blot-NBP2-50532-img0001.jpg "Western Blot: Enolase 2/Neuron-specific Enolase Antibody (NSEP1) [NBP2-50532] - Lysates were separated on SDS-PAGE and probed with Anti-NSE [NSE-P1]. Lane 1: SH-SY5Y, Lane 2: NT2/D1.")
![ELISA: CTLA-4 Antibody (9H10) - Chimeric [NBP3-11966] - Binding curves of the rabbit chimeric version of the anti-CTLA-4 antibody 9H10 (NBP3-11966; red line) and isotype control (anti-Fluorescein antibody NBP2-52638 4-4-20 (enhanced); blue line) to an ELISA plate coated with mouse CTLA-4-Fc fusion protein at a concentration of 5 ug/ml. A 3-fold serial dilution from 10,000 to 0.17 ng/ml was performed using NBP3-11966. For signal detection, a 1:4000 dilution of HRP-labelled anti-rabbit IgG1 antibody was used.](http://images.novusbio.com/fullsize/CTLA-4-Antibody-9H10-Chimeric-ELISA-NBP3-11966-img0001.jpg "ELISA: CTLA-4 Antibody (9H10) - Chimeric [NBP3-11966] - Binding curves of the rabbit chimeric version of the anti-CTLA-4 antibody 9H10 (NBP3-11966; red line) and isotype control (anti-Fluorescein antibody NBP2-52638 4-4-20 (enhanced); blue line) to an ELISA plate coated with mouse CTLA-4-Fc fusion protein at a concentration of 5 ug/ml. A 3-fold serial dilution from 10,000 to 0.17 ng/ml was performed using NBP3-11966. For signal detection, a 1:4000 dilution of HRP-labelled anti-rabbit IgG1 antibody was used.")
![Immunohistochemistry-Paraffin: CD45RA Antibody (SPM504) - IHC-Prediluted [NBP2-48453] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD45RA Monoclonal Antibody (SPM504).](http://images.novusbio.com/fullsize/CD45RA-Antibody-SPM504-IHC-Prediluted-Immunohistochemistry-Paraffin-NBP2-48453-img0001.jpg "Immunohistochemistry-Paraffin: CD45RA Antibody (SPM504) - IHC-Prediluted [NBP2-48453] - Formalin-fixed, paraffin-embedded human Tonsil stained with CD45RA Monoclonal Antibody (SPM504).")
![Western Blot: ER alpha/NR3A1 Antibody (ER505) - Azide and BSA Free [NBP2-33106] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).](http://images.novusbio.com/fullsize/ER-alpha-NR3A1-Antibody-ER505-Azide-and-BSA-Free-Western-Blot-NBP2-33106-img0003.jpg "Western Blot: ER alpha/NR3A1 Antibody (ER505) - Azide and BSA Free [NBP2-33106] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).")