| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-11923-25ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89254-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90470-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-97197-50ul | |||
![Immunohistochemistry: CACNA1G Antibody [NBP3-11923] - Immunohistochemical staining of human melanoma tumor tissue using CACNA1G antibody at 15 ug/ml.](http://images.novusbio.com/fullsize/CACNA1G-Antibody-Immunohistochemistry-NBP3-11923-img0001.jpg "Immunohistochemistry: CACNA1G Antibody [NBP3-11923] - Immunohistochemical staining of human melanoma tumor tissue using CACNA1G antibody at 15 ug/ml.")
![Immunocytochemistry/Immunofluorescence: BACE-1 Antibody (027) [NBP2-89254] - Staining of Human BACE1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human AK4 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/BACE-1-Antibody-027-Immunocytochemistry-Immunofluorescence-NBP2-89254-img0001.jpg "Immunocytochemistry/Immunofluorescence: BACE-1 Antibody (027) [NBP2-89254] - Staining of Human BACE1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-Human AK4 monoclonal antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.")
![Flow Cytometry: BACE-1 Antibody (027) [NBP2-89254] - Analysis of Human BACE1 expression on Jurkat cells. The cells were treated stained with purified anti-Human BACE1, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/BACE-1-Antibody-027-Flow-Cytometry-NBP2-89254-img0002.jpg)
![Western Blot: NFkB p100/p52 Antibody [NBP2-87904] - Host: Rabbit. Target Name: NFKB2. Sample Type: Jurkat Whole cell lysates. Antibody Dilution: 1.0ug/ml](http://images.novusbio.com/fullsize/NFkB-p100-p52-Antibody-Western-Blot-NBP2-87904-img0002.jpg "Western Blot: NFkB p100/p52 Antibody [NBP2-87904] - Host: Rabbit. Target Name: NFKB2. Sample Type: Jurkat Whole cell lysates. Antibody Dilution: 1.0ug/ml")
![Immunohistochemistry-Paraffin: NFkB p100/p52 Antibody [NBP2-87904] - Rabbit Anti-NFKB2 Antibody. Formalin Fixed Paraffin Embedded Tissue: Human Appendix (Colon) Tissue. Observed Staining: Cytoplasm. Primary Antibody Concentration: 1:100. Other Working Concentrations: 1:600.](http://images.novusbio.com/fullsize/NFkB-p100-p52-Antibody-Immunohistochemistry-Paraffin-NBP2-87904-img0001.jpg)
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0002.jpg "Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.")
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse heart with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0001.jpg)
![Immunohistochemistry-Paraffin: NDUFB9 Antibody [NBP2-97197] - Immunochemical staining of human NDUFB9 in human stomach with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/NDUFB9-Antibody-Immunohistochemistry-Paraffin-NBP2-97197-img0002.jpg "Immunohistochemistry-Paraffin: NDUFB9 Antibody [NBP2-97197] - Immunochemical staining of human NDUFB9 in human stomach with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: NDUFB9 Antibody [NBP2-97197] - Immunochemical staining of human NDUFB9 in human kidney with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/NDUFB9-Antibody-Immunohistochemistry-Paraffin-NBP2-97197-img0001.jpg)
![Immunocytochemistry/ Immunofluorescence: CD45 Antibody (PSH03-64) [NBP3-32448] - Immunocytochemistry analysis of Raji cells labeling CD45 with Mouse anti-CD45 antibody (NBP3-32448) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-CD45 antibody (NBP3-32448) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32448_mouse-cd45-mab-psh03-64-29202410334038.jpg "Immunocytochemistry/ Immunofluorescence: CD45 Antibody (PSH03-64) [NBP3-32448] - Immunocytochemistry analysis of Raji cells labeling CD45 with Mouse anti-CD45 antibody (NBP3-32448) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-CD45 antibody (NBP3-32448) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.")
![Flow Cytometry: CD45 Antibody (PSH03-64) [NBP3-32448] - Flow cytometric analysis of human PBMC labeling human CD45. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (NBP3-32448, 1μg/mL) (red). After incubation of the primary antibody at +4℃ for 30 minutes, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32448_mouse-cd45-mab-psh03-64-392024884642.jpg)
![Western Blot: PMP22 Antibody (JM52-30) [NBP2-67068] - Western blot analysis of PMP22 on PC-12 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/PMP22-Antibody-JM52-30-Western-Blot-NBP2-67068-img0005.jpg "Western Blot: PMP22 Antibody (JM52-30) [NBP2-67068] - Western blot analysis of PMP22 on PC-12 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: FOXE3 Antibody [NBP3-10932] - Immunohistochemical analysis of human muscle.](http://images.novusbio.com/fullsize/FOXE3-Antibody-Immunohistochemistry-NBP3-10932-img0001.jpg "Immunohistochemistry: FOXE3 Antibody [NBP3-10932] - Immunohistochemical analysis of human muscle.")
![Western Blot: Nav1.6 Antibody [NBP2-84176] - WB Suggested Anti-SCN8A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: Human Muscle](http://images.novusbio.com/fullsize/Nav1.6-Antibody-Western-Blot-NBP2-84176-img0001.jpg "Western Blot: Nav1.6 Antibody [NBP2-84176] - WB Suggested Anti-SCN8A Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: Human Muscle")
![Western Blot: Nav1.6 Antibody [NBP2-84176] - Host: Rabbit. Target Name: SCN8A. Sample Type: NCI-H226. Antibody Dilution: 1.0ug/mlSCN8A is supported by BioGPS gene expression data to be expressed in NCIH226](http://images.novusbio.com/fullsize/Nav1.6-Antibody-Western-Blot-NBP2-84176-img0002.jpg)
![Western Blot: Connexin 26/GJB2 Antibody [NBP2-88789] - WB Suggested Anti-GJB2 Antibody Titration: 1.25ug/ml. ELISA Titer: 1:62500. Positive Control: Human Lung](http://images.novusbio.com/fullsize/Connexin-26-GJB2-Antibody-Western-Blot-NBP2-88789-img0001.jpg "Western Blot: Connexin 26/GJB2 Antibody [NBP2-88789] - WB Suggested Anti-GJB2 Antibody Titration: 1.25ug/ml. ELISA Titer: 1:62500. Positive Control: Human Lung")
![Western Blot: Connexin 26/GJB2 Antibody [NBP2-88789] - WB Suggested Anti-GJB2 Antibody. Positive Control: Lane 1: 4ug mCx26 elution fraction 6 Lane 2: 4ug mCx26 elution fraction 7Lane 3: 4ug mCx26 elution fraction 6 + other Cx26 antibody Lane 4: 4ug mCx26 elution fraction 7 + other Cx26 antibody. Primary A](http://images.novusbio.com/fullsize/Connexin-26-GJB2-Antibody-Western-Blot-NBP2-88789-img0002.jpg)
![Western Blot: beta-Catenin [p Ser33, p Ser37] Antibody (JE59-59) [NBP3-32751] - Western blot analysis of beta-Catenin on different lysates with Rabbit anti-beta-Catenin antibody (NBP3-32751) at 1/1,000 dilution. Lane 1: 293T whole cell lysate Lane 2: 293T treated with 100nM Calyculin A for 15 minutes cell lysate Lane 3: C6 whole cell lysate Lane 4: C6 treated with 100nM Calyculin A for 30 minutes cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 85 kDa Observed band size: 100 kDa Exposure time: 5 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 (NBP3-32751) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32751_rabbit-beta-catenin-p-ser33-p-ser37-mab-je59-59-2782024163161.jpg "Western Blot: beta-Catenin [p Ser33, p Ser37] Antibody (JE59-59) [NBP3-32751] - Western blot analysis of beta-Catenin on different lysates with Rabbit anti-beta-Catenin antibody (NBP3-32751) at 1/1,000 dilution. Lane 1: 293T whole cell lysate Lane 2: 293T treated with 100nM Calyculin A for 15 minutes cell lysate Lane 3: C6 whole cell lysate Lane 4: C6 treated with 100nM Calyculin A for 30 minutes cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 85 kDa Observed band size: 100 kDa Exposure time: 5 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 (NBP3-32751) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:50,000 dilution was used for 1 hour at room temperature.")
![Flow Cytometry: CD133 Antibody (W6B3C1) [NBP3-09159] - Analysis (surface staining) of human peripheral whole blood showing CD133 positive stem cells (blue) and lymphocytes (red) stained using anti-CD133 (293C3) purified, GAM-FITC.](http://images.novusbio.com/fullsize/CD133-Antibody-W6B3C1-Flow-Cytometry-NBP3-09159-img0001.jpg "Flow Cytometry: CD133 Antibody (W6B3C1) [NBP3-09159] - Analysis (surface staining) of human peripheral whole blood showing CD133 positive stem cells (blue) and lymphocytes (red) stained using anti-CD133 (293C3) purified, GAM-FITC.")