NFAT5 Antibodies
We offer NFAT5 Antibodies for use in common research applications: Chromatin Immunoprecipitation, ELISA, Gel Super Shift Assays, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Immunoprecipitation, Western Blot. Each NFAT5 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our NFAT5 Antibodies can be used in a variety of model species: Hamster, Human, Mouse, Rabbit, Rat. Use the list below to choose the NFAT5 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our NFAT5 polyclonal antibodies.
Alternate Names for NFAT5 Antibodies
anti-NFAT5 antibody, anti-EC 3.6.1 antibody, anti-EC 3.6.3.14 antibody, anti-KIAA0827glutamine rich protein H65 antibody, anti-NF-AT5NFAT-like protein 1 antibody, anti-NFATL1 antibody, anti-NFATZ antibody, anti-nuclear factor of activated T-cells 5, tonicity-responsive antibody, anti-OREBP antibody, anti-osmotic response element-binding protein antibody, anti-T-cell transcription factor NFAT5 antibody, anti-TonE-binding protein antibody, anti-TonEBP antibody, anti-TONEBPnuclear factor of activated T-cells 5 antibody, anti-Tonicity-responsive enhancer-binding protein antibody
10 Results for "nfat5" in Primary Antibodies
![Western Blot: NFAT5 Antibody [NB120-3446] - Western blot image showing increased TonEBP/NFAT5 expression in response to hyperosmolarity (550mOsm/kg H2O) independently of Ift88 knockdown. Image collected and cropped by CiteAb from the following publication (nature.com/articles/s41598-019-51939-7), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NB120-3446-img0030.jpg "<b>Biological Strategies Validation. </b>Western Blot: NFAT5 Antibody [NB120-3446] - Western blot image showing increased TonEBP/NFAT5 expression in response to hyperosmolarity (550mOsm/kg H2O) independently of Ift88 knockdown. Image collected and cropped by CiteAb from the following publication (nature.com/articles/s41598-019-51939-7), licensed under a CC-BY license.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 using anti-NFAT5 polyclonal antibody (shown in green) in HeLa cells.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NB120-3446-img0025.jpg)
![Immunohistochemistry-Paraffin: NFAT5 Antibody [NB120-3446] - Normal biopsies of deparaffinized human skeletal muscle tissue.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunohistochemistry-Paraffin-NB120-3446-img0019.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 was performed by loading 25ug of various whole cell lysates onto a 4-20% Tris-HCl polyacrylamide gel. Proteins were transferred to a PVDF membrane and blocked with 5% Milk/TBST for at least 1 hour. Membranes were probed with a rabbit polyclonal antibody recognizing NFAT5 at a dilution of 1:1000 overnight at 4C on a rocking platform. Membranes were washed in TBS-0.1%Tween 20 and probed with a goat anti-rabbit-HRP secondary antibody at a dilution of 1:20,000 for at least one hour. Membranes were washed and chemiluminescent detection performed using Super Signal West Dura.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NB120-3446-img0021.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - Analysis of human NFAT5 from transfected BHK cell lysate.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NB120-3446-img0028.jpg)
![<b>Biological Strategies Validation. </b>Western Blot: NFAT5 Antibody [NB120-3446] - Western blot image and corresponding densitometry analyses showing TonEBP/NFAT5 levels under different osmotic conditions in wild-type and Kif3a null MEFs. Kif3a null MEFs show slightly attenuated hyperosmotic increase but unaffected hypoosmotic decrease in TonEBP expression. Image collected and cropped by CiteAb from the following publication (nature.com/articles/s41598-019-51939-7), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NB120-3446-img0029.jpg)
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 in HeLa Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a NFAT5 polyclonal antibody at a dilution of 1:20 overnight at 4C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. NFAT5 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NB120-3446-img0015.jpg)
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 in MCF-7 Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a NFAT5 polyclonal antibody at a dilution of 1:200 overnight at 4C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. NFAT5 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NB120-3446-img0016.jpg)
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 in NIH-3T3 Cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a NFAT5 polyclonal antibody at a dilution of 1:20 overnight at 4C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. NFAT5 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NB120-3446-img0017.jpg)
![Immunohistochemistry-Paraffin: NFAT5 Antibody [NB120-3446] - Normal biopsies of deparaffinized human brain tissue.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunohistochemistry-Paraffin-NB120-3446-img0018.jpg)
![Immunoprecipitation: NFAT5 Antibody [NB120-3446] - Analysis of NFAT5 was performed on U2OS cells. The antigen:antibody complex was formed by incubating 500ug whole cell lysate with 3ug of rabbit polyclonal antibody recognizing NFAT5 overnight on a rocking platform at 4C. The immune-complex was captured on 50ul Protein A/G Plus Agarose. Captured immune-complexes were washed and proteins eluted with 5X Reducing Sample Loading Dye. Samples were resolved on a 4-20% Tris-HCl polyacrylamide gel. Proteins were transferred to PVDF membrane and blocked with 5% Milk/TBS-0.1%Tween for at least 1 hour. Membranes were washed in TBS-0.1%Tween 20 and probed with a goat anti-rabbit-HRP secondary antibody at a dilution of 1:20,000 for at least one hour. Membranes were washed and chemiluminescent detection performed using Super Signal West Dura.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunoprecipitation-NB120-3446-img0026.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - Knockdown of Ift88 or Kif3a in NP cells does not affect hyperosmotic upregulation of TonEBP. (a) TonEBP/Nfat5 mRNA levels in NP cells with Ift88 knockdown (n ≥ 5). (b) Western blot image showing increased TonEBP expression in response to hyperosmolarity (550 mOsm/kg H2O) independently of Ift88 knockdown. (c) Densitometry analyses of TonEBP with Ift88 knockdown (n ≥ 4). (d) TonEBP/Nfat5 mRNA levels in NP cells with Kif3a knockdown (n ≥ 3). (e) Western blot image showing that hyperosmotic induction of TonEBP is maintained after Kif3a knockdown. (f) Densitometry analyses of TonEBP after Kif3a knockdown (n ≥ 4). Data are represented as scatter plots (mean ± SEM). ns = not significant. One-way ANOVA or Kruskal-Wallis test with Sidak’s or Dunn’s multiple comparison test was used based on the distribution of the data to determine statistical significance. Western blot images were cropped & acquired under same experimental conditions. See Supplementary Fig. S1-1 for un-cropped Western blot images. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31664118), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb120-3446_rabbit-polyclonal-nfat5-antibody-310202416212315.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - NP cells do not induce autophagy in response to hyperosmotic stimulus in an ex vivo disc organ culture model. (a) A schematic depicting ex vivo rat intervertebral disc organ culture model. (b) H&E & alcian blue staining of discs cultured under iso- (330 mOsm/kg H2O) or hyperosmotic (500 mOsm/kg H2O) conditions showing that NP maintained its structure & cellular morphology. Scale bar: 100 μm. (c) Western blot analysis of tissue proteins from NP or AF (annulus fibrosus) compartments of the organ culture discs. The level of TonEBP increased with hyperosmotic stimulus only in the NP. However, the levels of LC3-II, SQSTM1, ATG12-ATG5, BECN1, as well as pULK1 Ser757 did not change with hyperosmolarity in both NP & AF. (d–f) Densitometric analyses of multiple Western blots represented in (c). Bars represent mean ± SEM (n = 3; For each independent experiment, one motion segment per group was used for histology & 6 motion segments per group were used for tissue protein Western blot). Student t test was used to determine statistical significance. NS, non-significant. Western blot images were cropped & acquired under same experimental conditions. See Supplementary Fig. S1 for examples of uncropped images. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/28674405), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb120-3446_rabbit-polyclonal-nfat5-antibody-310202416205148.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - TonEBP does not control autophagy in NP cells. (a) Western blot analysis of NP cells transduced with a lentivirus expressing either control shRNA or shTonEBP plasmid showed that TonEBP silencing did not affect the levels of LC3-II, ATG12-ATG5, & BECN1. The levels of SQSTM1 increased with TonEBP silencing. (b–f) Densitometric analyses of multiple Western blots shown in (a). (g) Western blot analysis of ULK1 activation status showed that the levels of pULK1 Ser757 was slightly lower, while that of pULK1 Ser777 remained unaffected after TonEBP knockdown under hyperosmotic conditions. (h,i) Densitometric analyses of multiple western blots shown in (g). Bars represent mean ± SEM (n = 4). Two-way ANOVA with Tukey’s multiple comparisons test was used to determine statistical significance. NS, non-significant. Western blot images were cropped & acquired under same experimental conditions. See Supplementary Fig. S1 for examples of uncropped images. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/28674405), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb120-3446_rabbit-polyclonal-nfat5-antibody-31020241621813.jpg)
![Western Blot: NFAT5 Antibody [NB120-3446] - Hyperosmolarity does not upregulate the levels of canonical autophagic markers. (a) Western blot analysis of NP cells cultured under increasing osmolarity (330–600 mOsm/kg H2O) showed that the levels of LC3-II, SQSTM1, ATG12-ATG5, & BECN1 did not change by hyperosmolarity. However, TonEBP expression increased under hyperosmotic condition. (b–d) Densitometric analyses of multiple Western blots represented by (a) confirmed significant induction of TonEBP, while LC3-II & SQSTM1 levels remained unaltered (n = 5). (e) Western blot analysis of NP cells cultured under hyperosmotic condition for increasing lengths of time demonstrated that LC3-II, SQSTM1, ATG12-ATG5, & BECN1 levels were unaffected by hyperosmolarity up till 72 h. (f–i) Densitometric analyses of multiple Western blots shown in (e) (n = 3). Bars represent mean ± SEM. One-way ANOVA with Sidak’s multiple comparisons test was used to determine statistical significance. NS, non-significant. Western blot images were cropped & acquired under same experimental conditions. See Supplementary Fig. S1 for examples of uncropped images. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/28674405), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb120-3446_rabbit-polyclonal-nfat5-antibody-310202416212355.jpg)
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NBP2-49612] - Immunofluorescent staining of human cell line SiHa shows localization to nucleus.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-49612-img0003.jpg "Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NBP2-49612] - Immunofluorescent staining of human cell line SiHa shows localization to nucleus.")
![Western Blot: NFAT5 Antibody [NBP1-80257] - Host: Rabbit. Target Name: Nfat5. Sample Tissue: Mouse Skeletal Muscle. Antibody Dilution: 3ug/ml](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NBP1-80257-img0004.jpg "Western Blot: NFAT5 Antibody [NBP1-80257] - Host: Rabbit. Target Name: Nfat5. Sample Tissue: Mouse Skeletal Muscle. Antibody Dilution: 3ug/ml")
![Western Blot: NFAT5 Antibody [NBP1-80257] - SP2/0 cell lysate, concentration 0.2-1 ug/ml.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NBP1-80257-img0002.jpg)
![Western Blot: NFAT5 Antibody [NBP1-80257] - Lanes: Lane 1 : 20 ug HT 29 lysate blocked with 5% FBS Lane 2: 20 ug HT 29 lysate blocked with no FBS Lane 3: 20 ug HT-29 lyaste blocked with no PBS + 100 mM NaCl Primary, Antibody Dilution: 1 : 1000 Secondary Antibody: Goat anti-rabbit-HRP Secondary, Antibody Dilution: 1 : 1000 Gene name: NFAT5.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-NBP1-80257-img0003.jpg)
![Western Blot: NFAT5 Antibody [H00010725-B01P] - Analysis of NFAT5 expression in transfected 293T cell line by NFAT5 polyclonal antibody. Lane 1: NFAT5 transfected lysate(163.24 KDa). Lane 2: Non-transfected lysate.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Western-Blot-H00010725-B01P-img0002.jpg "Western Blot: NFAT5 Antibody [H00010725-B01P] - Analysis of NFAT5 expression in transfected 293T cell line by NFAT5 polyclonal antibody. Lane 1: NFAT5 transfected lysate(163.24 KDa). Lane 2: Non-transfected lysate.")
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [H00010725-B01P] - Analysis of purified antibody to NFAT5 on HeLa cell. (antibody concentration 30 ug/ml)](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-H00010725-B01P-img0001.jpg)
![Immunoprecipitation:NFAT5 AntibodyNBP3-30029] -Detection of human NFAT5 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-NFAT5 antibody NBP3-30029 (lot NBP3-30029-1) used for IP at 6 µg per reaction. NFAT5 was also immunoprecipitated by rabbit anti-NFAT5.. For blotting immunoprecipitated NFAT5, NBP3-30029 was used at 0.4 µg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/nbp3-30029_rabbit-nfat5-pab-3012202417405811.jpg "Immunoprecipitation:NFAT5 AntibodyNBP3-30029] -Detection of human NFAT5 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-NFAT5 antibody NBP3-30029 (lot NBP3-30029-1) used for IP at 6 µg per reaction. NFAT5 was also immunoprecipitated by rabbit anti-NFAT5.. For blotting immunoprecipitated NFAT5, NBP3-30029 was used at 0.4 µg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")
![Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NBP2-56674] - Staining of human cell line A549 shows localization to nucleoplasm.](http://images.novusbio.com/fullsize/NFAT5-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-56674-img0001.jpg "Immunocytochemistry/Immunofluorescence: NFAT5 Antibody [NBP2-56674] - Staining of human cell line A549 shows localization to nucleoplasm.")
![Western Blot: NFAT5 Antibody [NBP3-35688] - Western blot analysis of various lysates using NFAT5 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated 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.Exposure time: 60s.](http://images.novusbio.com/fullsize/nbp3-35688_rabbit-nfat5-pab-912202415171133.jpg "Western Blot: NFAT5 Antibody [NBP3-35688] - Western blot analysis of various lysates using NFAT5 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated 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.Exposure time: 60s.")
![Immunoprecipitation:NFAT5 AntibodyNBP3-30150] -Detection of human NFAT5 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-NFAT5 antibody NBP3-30150 (lot NBP3-30150-1) used for IP at 6 µg per reaction. NFAT5 was also immunoprecipitated by rabbit anti-NFAT5.. For blotting immunoprecipitated NFAT5, NBP3-30150 was used at 1 µg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/nbp3-30150_rabbit-nfat5-pab-3012202416181816.jpg "Immunoprecipitation:NFAT5 AntibodyNBP3-30150] -Detection of human NFAT5 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-NFAT5 antibody NBP3-30150 (lot NBP3-30150-1) used for IP at 6 µg per reaction. NFAT5 was also immunoprecipitated by rabbit anti-NFAT5.. For blotting immunoprecipitated NFAT5, NBP3-30150 was used at 1 µg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")