| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05539-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-86654-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-85498-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72192 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-75514-0.025mg | |||
![Immunohistochemistry-Paraffin: C-Peptide Antibody (HL1158) - Azide and BSA Free [NBP3-25420] - C-Peptide antibody [HL1158] detects secreted C-Peptide protein by immunohistochemical analysis. Sample: Paraffin-embedded human pancreas. C-Peptide stained by C-Peptide antibody [HL1158] (NBP3-25420) diluted at 1:10000. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25420_rabbit-c-peptide-mab-hl1158-azide-and-bsa-free-212024939186.jpg "Immunohistochemistry-Paraffin: C-Peptide Antibody (HL1158) - Azide and BSA Free [NBP3-25420] - C-Peptide antibody [HL1158] detects secreted C-Peptide protein by immunohistochemical analysis. Sample: Paraffin-embedded human pancreas. C-Peptide stained by C-Peptide antibody [HL1158] (NBP3-25420) diluted at 1:10000. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min")
![ELISA: C-Peptide Antibody (HL1158) - Azide and BSA Free [NBP3-25420] - Indirect ELISA analysis performed by coating plate with recombinant mature C-Peptide protein (19.05-0.3 nM). Coated protein was probed with C-Peptide antibody [HL1158] (NBP3-25420) (1 ug/mL). Goat anti-rabbit IgG antibody (HRP) (1:10000) was used to detect bound primary antibody.](http://images.novusbio.com/fullsize/nbp3-25420_rabbit-c-peptide-mab-hl1158-azide-and-bsa-free-212024939170.jpg)
![C-Peptide antibody [HL1158] detects C-Peptide protein by immunohistochemical analysis.Sample: Paraffin-embedded mouse pancreas.C-Peptide stained by C-Peptide antibody [HL1158] (NBP3-25420) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25420_rabbit-c-peptide-mab-hl1158-azide-and-bsa-free-immunohistochemistry-paraffin-26112025182534.jpg)
![C-Peptide antibody [HL1158] detects C-Peptide protein by immunohistochemical analysis.Sample: Paraffin-embedded rat pancreas.C-Peptide stained by C-Peptide antibody [HL1158] (NBP3-25420) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-25420_rabbit-c-peptide-mab-hl1158-azide-and-bsa-free-immunohistochemistry-paraffin-2611202518213322.jpg)
![Western Blot: MAT1/2A Antibody (HL1679) - Azide and BSA Free [NBP3-25557] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody [HL1679] (NBP3-25557) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25557_rabbit-mat1-2a-mab-hl1679-azide-and-bsa-free-212024940892.jpg "Western Blot: MAT1/2A Antibody (HL1679) - Azide and BSA Free [NBP3-25557] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody [HL1679] (NBP3-25557) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Western Blot: MAT1/2A Antibody (HL1679) - Azide and BSA Free [NBP3-25557] - Drosophila tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody [HL1679] (NBP3-25557) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25557_rabbit-mat1-2a-mab-hl1679-azide-and-bsa-free-2120249383121.jpg)
![Western Blot: MAT1/2A Antibody (HL1679) - Azide and BSA Free [NBP3-25557] - 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody [HL1679] (NBP3-25557) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25557_rabbit-mat1-2a-mab-hl1679-azide-and-bsa-free-2120249415951.jpg)
![Western Blot: MAT1/2A Antibody (HL1679) - Azide and BSA Free [NBP3-25557] - Various tissue extracts (50 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT1A + MAT2A antibody [HL1679] (NBP3-25557) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25557_rabbit-mat1-2a-mab-hl1679-azide-and-bsa-free-2120249355542.jpg)
![Western Blot: MARCKS Antibody [NBP3-05539] - Western blot analysis of different cell lysates using MARCKS Antibody in green: [1] protein standard, [2] NIH-3T3, [3] HEK293, [4] HeLa, [5] SH-SY5Y, [6] C6 and [7] COS1 cells. The band at about 80kDa corresponds to the MARCKS protein detected only in the human and monkey cells. The antibody does not recognize the rodent form of the MARCKS protein.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Western-Blot-NBP3-05539-img0002.jpg "Western Blot: MARCKS Antibody [NBP3-05539] - Western blot analysis of different cell lysates using MARCKS Antibody in green: [1] protein standard, [2] NIH-3T3, [3] HEK293, [4] HeLa, [5] SH-SY5Y, [6] C6 and [7] COS1 cells. The band at about 80kDa corresponds to the MARCKS protein detected only in the human and monkey cells. The antibody does not recognize the rodent form of the MARCKS protein.")
![Immunocytochemistry/Immunofluorescence: MARCKS Antibody [NBP3-05539] - Immunofluorescent analysis of HeLa cell culture stained with MARCKS Antibody at a dilution of 1:1,000 in red, and costained with chicken pAb to vimentin at a dilution of 1:10,000 in green. The blue is Hoechst staining of nuclear DNA. MARCKS antibody binds to MARCKS protein expressed in the membrane structures and in cytoplasm, while the vimentin antibody stains the intermediate filaments.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05539-img0001.jpg)
![Western Blot: MARCKS Antibody [NBP3-05540] - Western blot analysis of different cell lines lysates using MARCKS, at a dilution of 1:1,000 in green: [1] protein standard (red), [2] HEK293, [3] HeLa, [4] SH-SY5Y, and [5] COS1 cells. Strong band at 80kDa corresponds to MARCKS protein. The same blot was simultaneously probed with mouse mAb to GAPDH at a dilution of 1:5,000 in red, which reveals a single band at 37kDa in all preparations.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Western-Blot-NBP3-05540-img0002.jpg "Western Blot: MARCKS Antibody [NBP3-05540] - Western blot analysis of different cell lines lysates using MARCKS, at a dilution of 1:1,000 in green: [1] protein standard (red), [2] HEK293, [3] HeLa, [4] SH-SY5Y, and [5] COS1 cells. Strong band at 80kDa corresponds to MARCKS protein. The same blot was simultaneously probed with mouse mAb to GAPDH at a dilution of 1:5,000 in red, which reveals a single band at 37kDa in all preparations.")
![Immunocytochemistry/Immunofluorescence: MARCKS Antibody [NBP3-05540] - Immunofluorescent analysis of HeLa cells stained with MARCKS Antibody at a dilution of 1:5,000 in red, and costained with mouse mAb to beta-tubulin at a dilution of 1:10,000 in green. The blue is Hoechst staining of nuclear DNA. The MARCKS antibody binds to MARCKS protein expressed in the plasma membrane and cytoplasm, while the beta-tubulin antibody stains cytoplasmic microtubules.](http://images.novusbio.com/fullsize/MARCKS-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-05540-img0001.jpg)
![Immunohistochemistry-Paraffin: Carbonic Anhydrase VIII/CA8 Antibody [NBP1-86654] - Immunohistochemical staining of human cerebellum shows strong cytoplasmic positivity in purkinje cells.](http://images.novusbio.com/fullsize/Carbonic-Anhydrase-VIII-CA8-Antibody-Immunohistochemistry-Paraffin-NBP1-86654-img0001.jpg "Immunohistochemistry-Paraffin: Carbonic Anhydrase VIII/CA8 Antibody [NBP1-86654] - Immunohistochemical staining of human cerebellum shows strong cytoplasmic positivity in purkinje cells.")
![Immunocytochemistry/Immunofluorescence: COX4 Antibody [NBP1-85498] - Immunofluorescent staining of human cell line U-2 OS shows localization to nucleus & mitochondria.](http://images.novusbio.com/fullsize/COX4-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-85498-img0006.jpg "Immunocytochemistry/Immunofluorescence: COX4 Antibody [NBP1-85498] - Immunofluorescent staining of human cell line U-2 OS shows localization to nucleus & mitochondria.")
![Immunohistochemistry-Paraffin: COX4 Antibody [NBP1-85498] - Staining of human kidney shows moderate granular positivity in renal tubules.](http://images.novusbio.com/fullsize/COX4-Antibody-Immunohistochemistry-Paraffin-NBP1-85498-img0005.jpg)
![Western Blot: IPMK Antibody (HL2244) - Azide and BSA Free [NBP3-25536] - Various tissue extracts (50 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with IPMK antibody [HL2244] (NBP3-25536) diluted at 1:4000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25536_rabbit-ipmk-mab-hl2244-azide-and-bsa-free-2120249432844.jpg "Western Blot: IPMK Antibody (HL2244) - Azide and BSA Free [NBP3-25536] - Various tissue extracts (50 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with IPMK antibody [HL2244] (NBP3-25536) diluted at 1:4000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Genetic Strategies Validation. </b>Western Blot: IPMK Antibody (HL2244) - Azide and BSA Free [NBP3-25536] - Non-transfected (-) and transfected (+) A431 whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with IPMK antibody [HL2244] (NBP3-25536) diluted at 1:4000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25536_rabbit-ipmk-mab-hl2244-azide-and-bsa-free-2120249351384.jpg)
![Western Blot: IPMK Antibody (HL2244) - Azide and BSA Free [NBP3-25536] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with IPMK antibody [HL2244] (NBP3-25536) diluted at 1:500000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25536_rabbit-ipmk-mab-hl2244-azide-and-bsa-free-2120249355582.jpg)
![Western Blot: IPMK Antibody (HL2244) - Azide and BSA Free [NBP3-25536] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with IPMK antibody [HL2244] (NBP3-25536) diluted at 1:5000. 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/nbp3-25536_rabbit-ipmk-mab-hl2244-azide-and-bsa-free-2120249432883.jpg)
![Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Ferritin Heavy Chain antibody [HL1905] (NBP3-48666) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48666_rabbit-ferritin-heavy-chain-mab-hl1905-western-blot-1411202518351214.jpg "Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Ferritin Heavy Chain antibody [HL1905] (NBP3-48666) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![<b>Orthogonal Strategies Validation. </b>Various whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with Ferritin Heavy Chain antibody [HL1905] (NBP3-48666) diluted at 1:3000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.](http://images.novusbio.com/fullsize/nbp3-48666_rabbit-ferritin-heavy-chain-mab-hl1905-western-blot-1411202518363623.jpg)
![Non-transfected (-) and transfected (+) 293T whole cell extracts were separated by 15% SDS-PAGE, and the membrane was blotted with Ferritin Heavy Chain antibody [HL1905] (NBP3-48666) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48666_rabbit-ferritin-heavy-chain-mab-hl1905-western-blot-1411202518321623.jpg)
![Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Ferritin Heavy Chain antibody [HL1905] (NBP3-48666) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48666_rabbit-ferritin-heavy-chain-mab-hl1905-western-blot-141120251840439.jpg)
![Western Blot: FA2H Antibody (OTI2E3) [NBP2-45564] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY FA2H.](http://images.novusbio.com/fullsize/FA2H-Antibody-OTI2E3-Western-Blot-NBP2-45564-img0002.jpg "Western Blot: FA2H Antibody (OTI2E3) [NBP2-45564] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY FA2H.")
![Immunofluorescence: FA2H Antibody (OTI2E3) [NBP2-45564] - Analysis of COS7 cells transiently transfected with pCMV6-ENTRY FA2H.](http://images.novusbio.com/fullsize/FA2H-Antibody-OTI2E3-Immunofluorescence-NBP2-45564-img0001.jpg)
![Western Blot: XBP1 Antibody (3H1G4) [NBP1-75514] - analysis of 100 ng of XBP-1 recombinant protein with XBP-1 antibody at 1 ug/mL.](http://images.novusbio.com/fullsize/XBP1-Antibody-3H1G4-Western-Blot-NBP1-75514-img0001.jpg "Western Blot: XBP1 Antibody (3H1G4) [NBP1-75514] - analysis of 100 ng of XBP-1 recombinant protein with XBP-1 antibody at 1 ug/mL.")
![Immunocytochemistry/ Immunofluorescence: XBP1 Antibody (3H1G4) - BSA Free [NBP1-75514] - Immunofluorescence of XBP1 in HepG2 cells with XBP1 antibody at 4 u/mL.](http://images.novusbio.com/fullsize/nbp1-75514_mouse-monoclonal-xbp1-antibody-3h1g4-2711202419353897.jpg)
![Immunocytochemistry/ Immunofluorescence: XBP1 Antibody (3H1G4) - BSA Free [NBP1-75514] - Immunocytochemistry of XBP1 in HepG2 cells with XBP1 antibody at 2 u/mL.](http://images.novusbio.com/fullsize/nbp1-75514_mouse-monoclonal-xbp1-antibody-3h1g4-271120241918648.jpg)
![Western Blot: Cytochrome P450 2E1 Antibody [NBP1-52087] - Analysis of Cytochrome P450 2E1 in Human Liver lysate (35ug protein in RIPA buffer) using NBP1-52087 at 0.05 ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Cytochrome-P450-2E1-Antibody-Western-Blot-NBP1-52087-img0004.jpg "Western Blot: Cytochrome P450 2E1 Antibody [NBP1-52087] - Analysis of Cytochrome P450 2E1 in Human Liver lysate (35ug protein in RIPA buffer) using NBP1-52087 at 0.05 ug/ml. Primary incubation was 1 hour. Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: Cytochrome P450 2E1 Antibody [NBP1-52087] - (3.8ug/ml) staining of paraffin embedded Human Liver. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.](http://images.novusbio.com/fullsize/Cytochrome-P450-2E1-Antibody-Immunohistochemistry-Paraffin-NBP1-52087-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells,permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL). The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/xCT-Antibody-Immunocytochemistry-Immunofluorescence-NB100-59735-img0001.jpg "Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed A549 cells,permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL). The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).")
![Immunocytochemistry/Immunofluorescence: xCT Antibody [NB100-59735] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing vesicle staining. The nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](http://images.novusbio.com/fullsize/xCT-Antibody-Immunocytochemistry-Immunofluorescence-NB100-59735-img0002.jpg)