| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05011-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB300-339-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-75290-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NB110-93606-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-12283-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-06199-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99740-50ul | |||
![Western Blot: GALP Antibody [NBP3-04896] - Analysis of extracts of U-87MG cells, using GALP antibody at 1:3000 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 Enhanced Kit](http://images.novusbio.com/fullsize/GALP-Antibody-Western-Blot-NBP3-04896-img0001.jpg "Western Blot: GALP Antibody [NBP3-04896] - Analysis of extracts of U-87MG cells, using GALP antibody at 1:3000 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 Enhanced Kit")
![Western Blot: LEPREL1 Antibody [NBP3-05011] - Analysis of extracts of NCI-H460 cells, using LEPREL1 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/LEPREL1-Antibody-Western-Blot-NBP3-05011-img0001.jpg "Western Blot: LEPREL1 Antibody [NBP3-05011] - Analysis of extracts of NCI-H460 cells, using LEPREL1 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")
![Western Blot: alpha-Synuclein [p Ser129] Antibody [NBP3-05429] - Western blot analysis of extracts from mouse brain tissue, using alpha-Synuclein antibody (NBP3-05429). Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA.](http://images.novusbio.com/fullsize/alpha-Synuclein-[p-Ser129]-Antibody-Western-Blot-NBP3-05429-img0001.jpg "Western Blot: alpha-Synuclein [p Ser129] Antibody [NBP3-05429] - Western blot analysis of extracts from mouse brain tissue, using alpha-Synuclein antibody (NBP3-05429). Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA.")
![Western Blot: F-Spondin/SPON1 Antibody [NB300-339] - E coli-derived fusion protein as test antigen. Affi-anti- SPON1 IgY dilution: 1:2000, Goat anti-IgY-HRP dilution: 1:1000. Colorimetric method for signal development. ( anti-SPON1 )](http://images.novusbio.com/fullsize/F-Spondin-SPON1-Antibody-Western-Blot-NB300-339-img0002.jpg "Western Blot: F-Spondin/SPON1 Antibody [NB300-339] - E coli-derived fusion protein as test antigen. Affi-anti- SPON1 IgY dilution: 1:2000, Goat anti-IgY-HRP dilution: 1:1000. Colorimetric method for signal development. ( anti-SPON1 )")
![Immunohistochemistry-Paraffin: EphA7 Antibody (6E1) [NB110-93606] - The Kidney tissue samples from the Folic Acid induced kidney injury model were fixed using 4% PFA at 4C for overnight and embeded in paraffin. 4um section was sublected to IHC with NB110-93606](http://images.novusbio.com/fullsize/EphA7-Antibody-6E1-Immunohistochemistry-Paraffin-NB110-93606-img0001.jpg "Immunohistochemistry-Paraffin: EphA7 Antibody (6E1) [NB110-93606] - The Kidney tissue samples from the Folic Acid induced kidney injury model were fixed using 4% PFA at 4C for overnight and embeded in paraffin. 4um section was sublected to IHC with NB110-93606")
![Immunohistochemistry-Paraffin: Ephrin-B3 Antibody (MM0264- 12X1) [NBP2-12283] - 10% Buffer formalin fixed and parffine embedded human placetal tissue section (4um) is subjected IHC staining using NBP2-12283. Tissue section was pretreated in citric buffer (pH 6.0) with microwave for antige retrieval before IHC is applied.](http://images.novusbio.com/fullsize/Ephrin-B3-Antibody-MM0264-12X1-Immunohistochemistry-Paraffin-NBP2-12283-img0001.jpg "Immunohistochemistry-Paraffin: Ephrin-B3 Antibody (MM0264- 12X1) [NBP2-12283] - 10% Buffer formalin fixed and parffine embedded human placetal tissue section (4um) is subjected IHC staining using NBP2-12283. Tissue section was pretreated in citric buffer (pH 6.0) with microwave for antige retrieval before IHC is applied.")
![Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) at 1/200 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 (NBP3-32984) at 1/200 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/nbp3-32984_rabbit-substance-p-mab-je59-73-298202414115438.jpg "Immunohistochemistry: Substance P Antibody (JE59-73) [NBP3-32984] - Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue with Rabbit anti-Substance P antibody (NBP3-32984) at 1/200 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 (NBP3-32984) at 1/200 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.")
![Immunohistochemistry-Paraffin: Hippocalcin Antibody [NBP3-06199] - Immunochemical staining of human HPCA in cynomolgus cerebellum with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/Hippocalcin-Antibody-Immunohistochemistry-Paraffin-NBP3-06199-img0002.jpg "Immunohistochemistry-Paraffin: Hippocalcin Antibody [NBP3-06199] - Immunochemical staining of human HPCA in cynomolgus cerebellum with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: Hippocalcin Antibody [NBP3-06199] - Immunochemical staining of human HPCA in human brain with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/Hippocalcin-Antibody-Immunohistochemistry-Paraffin-NBP3-06199-img0001.jpg)
![Western Blot: CRABP2 Antibody [NBP2-99740] - Anti-CRABP2 rabbit polyclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 16 kDa. Observed band size: 14 kDa](http://images.novusbio.com/fullsize/CRABP2-Antibody-Western-Blot-NBP2-99740-img0004.jpg "Western Blot: CRABP2 Antibody [NBP2-99740] - Anti-CRABP2 rabbit polyclonal antibody at 1:500 dilution. Lane A: MCF7 Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 16 kDa. Observed band size: 14 kDa")
![Western Blot: CRABP2 Antibody [NBP2-99740] - CRABP2 was immunoprecipitated using: Lane A: 0.5 mg MCF-7 Whole Cell Lysate 2 ul anti-CRABP2 rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-CRABP2 rabbit polyclonal antibody, at 1:200 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 16 kDa. Observed band size: 16 kDa](http://images.novusbio.com/fullsize/CRABP2-Antibody-Western-Blot-NBP2-99740-img0003.jpg)
![Western Blot: MT-ND1 Antibody (JE34-93) [NBP3-32613] - Western blot analysis of MT-ND1 on different lysates with Rabbit anti-MT-ND1 antibody (NBP3-32613) at 1/1,000 dilution. Lane 1: Mouse heart tissue lysate Lane 2: Rat heart tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 36 kDa Observed band size: 37 kDa Exposure time: 43 seconds; 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 (NBP3-32613) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. 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/nbp3-32613_rabbit-mt-nd1-mab-je34-93-27820241631638.jpg "Western Blot: MT-ND1 Antibody (JE34-93) [NBP3-32613] - Western blot analysis of MT-ND1 on different lysates with Rabbit anti-MT-ND1 antibody (NBP3-32613) at 1/1,000 dilution. Lane 1: Mouse heart tissue lysate Lane 2: Rat heart tissue lysate Lysates/proteins at 30 ug/Lane. Predicted band size: 36 kDa Observed band size: 37 kDa Exposure time: 43 seconds; 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 (NBP3-32613) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")