| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05539-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-86654-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB600-772-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-75514-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-65388-0.025mg | |||
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody [NBP3-13324] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Acetyl-CoA Carboxylase alpha/ACACA (phospho Ser79) antibody (NBP3-13324) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Acetyl-CoA-Carboxylase-alpha-ACACA-[p-Ser79]-Antibody-Western-Blot-NBP3-13324-img0003.jpg "Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody [NBP3-13324] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Acetyl-CoA Carboxylase alpha/ACACA (phospho Ser79) antibody (NBP3-13324) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Biological Strategies Validation. </b>Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody [NBP3-13324] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Acetyl-CoA Carboxylase alpha/ACACA (phospho Ser79) antibody (NBP3-13324) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Acetyl-CoA-Carboxylase-alpha-ACACA-[p-Ser79]-Antibody-Western-Blot-NBP3-13324-img0001.jpg)
![Western Blot: Acetyl-CoA Carboxylase alpha/ACACA [p Ser79] Antibody [NBP3-13324] - Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Acetyl-CoA Carboxylase alpha/ACACA antibody (NBP3-13324) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-13324_rabbit-acetyl-coa-carboxylase-alpha-acaca-p-ser-79-pab-910202419593567.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](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.")
![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)
![Flow Cytometry: CD98 Antibody (44D7) [NB600-772] - A surface stain was performed on K562 cells with CD98 (44D7) antibody NB600-772 (blue) and a matched isotype control (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems).](http://images.novusbio.com/fullsize/CD98-Antibody-44D7-Flow-Cytometry-NB600-772-img0006.jpg "Flow Cytometry: CD98 Antibody (44D7) [NB600-772] - A surface stain was performed on K562 cells with CD98 (44D7) antibody NB600-772 (blue) and a matched isotype control (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems).")
![Flow Cytometry: CD98 Antibody (44D7) [NB600-772] - Staining of human peripheral blood monocytes with mouse anti human CD98, using F(ab')2 rabbit anti mouse IgG: FITC (STAR9B) as a secondary antibody.](http://images.novusbio.com/fullsize/CD98-Antibody-44D7-Flow-Cytometry-NB600-772-img0001.jpg)
![Flow Cytometry: CD98 Antibody (44D7) [NB600-772] - Analysis using the FITC conjugate of NB600-772. Staining of human peripheral blood monocytes](http://images.novusbio.com/fullsize/CD98-Antibody-44D7-Flow-Cytometry-NB600-772-img0004.jpg)
![Flow Cytometry: CD98 Antibody (44D7) [NB600-772] - Analysis using the PE conjugate of NB600-772. Staining of human peripheral blood monocytes with mouse anti human CD98: RPE.](http://images.novusbio.com/fullsize/CD98-Antibody-44D7-Flow-Cytometry-NB600-772-img0005.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)
![Flow Cytometry: L-Selectin/CD62L Antibody (FMC46) [NB100-65388] - Flow Cytometry: L-Selectin/CD62L Antibody (FMC46) [PerCP] [NB100-65388PCP] - A cell surface stain was performed on human peripheral blood lymphocytes with L-Selectin/CD62L (FMC46) antibody NB100-65388PCP (blue) and a matched isotype control NBP2-27231PCP (orange). Cells were incubated in an antibody dilution of 5 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Peridinin-Chlorophyll-Protein complex. Image using the PerCP form of this antibody.](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-FMC46-Flow-Cytometry-NB100-65388-img0003.jpg "Flow Cytometry: L-Selectin/CD62L Antibody (FMC46) [NB100-65388] - Flow Cytometry: L-Selectin/CD62L Antibody (FMC46) [PerCP] [NB100-65388PCP] - A cell surface stain was performed on human peripheral blood lymphocytes with L-Selectin/CD62L (FMC46) antibody NB100-65388PCP (blue) and a matched isotype control NBP2-27231PCP (orange). Cells were incubated in an antibody dilution of 5 ug/mL for 20 minutes at room temperature. Both antibodies were conjugated to Peridinin-Chlorophyll-Protein complex. Image using the PerCP form of this antibody.")
![Flow Cytometry: L-Selectin/CD62L Antibody (FMC46) [NB100-65388] - Staining of human peripheral blood granulocytes with Mouse anti Human CD62L:FITC](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-FMC46-Flow-Cytometry-NB100-65388-img0002.jpg)