| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05539-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-85498-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-75514-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB300-558-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-72378 | |||
![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)
![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: 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: 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)
![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)
![Western Blot: ACSL1 Antibody (HL1530) - Azide and BSA Free [NBP3-25351] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ACSL1 antibody [HL1530] (NBP3-25351) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25351_rabbit-acsl1-mab-hl1530-azide-and-bsa-free-2120249362781.jpg "Western Blot: ACSL1 Antibody (HL1530) - Azide and BSA Free [NBP3-25351] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ACSL1 antibody [HL1530] (NBP3-25351) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Western Blot: ACSL1 Antibody (HL1530) - Azide and BSA Free [NBP3-25351] - Various tissue extracts (50 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ACSL1 antibody [HL1530] (NBP3-25351) diluted at 1:20000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25351_rabbit-acsl1-mab-hl1530-azide-and-bsa-free-212024939156.jpg)
![Western Blot: ACSL1 Antibody (HL1530) - Azide and BSA Free [NBP3-25351] - Rat tissue extract (50 ug) was separated by 7.5% SDS-PAGE, and the membrane was blotted with ACSL1 antibody [HL1530] (NBP3-25351) diluted at 1:20000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-25351_rabbit-acsl1-mab-hl1530-azide-and-bsa-free-2120249342734.jpg)
![<b>Orthogonal Strategies Validation. </b>Western Blot: ACSL1 Antibody (HL1530) - Azide and BSA Free [NBP3-25351] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ACSL1 antibody [HL1530] (NBP3-25351) diluted at 1:2000. 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/nbp3-25351_rabbit-acsl1-mab-hl1530-azide-and-bsa-free-212024941450.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: CETP Antibody (ATM192) [NB300-558] - Analysis of human liver extract.](http://images.novusbio.com/fullsize/CETP-Antibody-ATM192-Western-Blot-NB300-558-img0005.jpg "Western Blot: CETP Antibody (ATM192) [NB300-558] - Analysis of human liver extract.")
![Immunocytochemistry/Immunofluorescence: CETP Antibody (ATM192) [NB300-558] - Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a CETP monoclonal antibody at a dilution of 1:20 overnight at 4 C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/CETP-Antibody-ATM192-Immunocytochemistry-Immunofluorescence-NB300-558-img0004.jpg)
![Western Blot: Calcium Activated Nucleotidase 1/CANT1 Antibody (7F8) [NBP2-46056] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Calcium Activated Nucleotidase 1.](http://images.novusbio.com/fullsize/Calcium-Activated-Nucleotidase-1-CANT1-Antibody-7F8-Western-Blot-NBP2-46056-img0003.jpg "Western Blot: Calcium Activated Nucleotidase 1/CANT1 Antibody (7F8) [NBP2-46056] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Calcium Activated Nucleotidase 1.")
![Immunohistochemistry: Calcium Activated Nucleotidase 1/CANT1 Antibody (7F8) [NBP2-46056] - Analysis of Carcinoma of Human liver tissue.(Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/Calcium-Activated-Nucleotidase-1-CANT1-Antibody-7F8-Immunohistochemistry-NBP2-46056-img0002.jpg)
![Immunohistochemistry: Calcium Activated Nucleotidase 1/CANT1 Antibody (7F8) [NBP2-46056] - Analysis of Human liver tissue. (Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/Calcium-Activated-Nucleotidase-1-CANT1-Antibody-7F8-Immunohistochemistry-NBP2-46056-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).](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)