| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-304SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-305SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-904SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-03993SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-18336-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-18333-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-18335-0.025mg | |||
![Depletion of PNUTS and NPAT induces a global DDR.(A) Induction of telomere dysfunction–induced foci (TIF) upon candidate knockdown in HeLa cells from Fig 5. Depletion of TRF2 was used as a positive control. 53BP1 was detected by indirect IF and telomeres by FISH with a Cy3-[CCCTAA]3 probe. (B) Frequency distribution of the number of TIFs per cell from (A). n indicates the number of cells analyzed for each condition and red lines mark the mean.](http://images.novusbio.com/fullsize/nb100-304_rabbit-polyclonal-53bp1-antibody-271220231261934.jpg)
![CO attenuates mitochondrial dysfunction-derived sterile inflammation through TFEB-mediated mitophagy and mitochondrial biogenesis.Mice were exposed to LPS/D-galactosamine (D-GalN) with or without CO (250 ppm, 2 h/day) pretreatment, the blood and liver samples were collected 2 h and 6 h (b–i) after LPS/D-GalN administration. a The levels of ALT and AST were determined. Data are shown as mean ± SEM (n = 5). ***P < 0.001. b Liver sections were stained with H&E for morphological evaluation. c The levels of serum IL-1 beta were measured by ELISA. Data are shown as mean ± SEM (n = 4). **P < 0.01. ***P < 0.001. d Cytosolic mtDNA amounts in liver tissues were measured by qRT-PCR. Data are shown as mean ± SEM (n = 4). *P < 0.05. e Cleaved caspase-1 in cell lysates isolated from liver tissues was analyzed by immunoblotting. f The level of nuclear TFEB in liver tissues was determined by immunoblotting. Lamin B served as the nuclear standard. g Mitochondrial fractionation in liver tissues was analyzed by immunoblotting using antibodies against PINK1, Parkin, and LC3B-II. COX IV was used as marker for mitochondrial fractions. h, i The levels of autophagy-related genes and lysosomal genes (h) or mitochondrial biogenesis-associated genes (i) expressed in liver tissues were analyzed by qRT-PCR. Data are shown as mean ± SEM (n = 4). *P < 0.05, **P < 0.01. ***P < 0.001. j A scheme for the mechanisms of attenuating LSP/D-GalN-induced liver failure by CO through maintaining the balance between mitophagy and mitochondrial biogenesis. CO/CORM inhibits complexes of the mitochondrial respiratory chain (1) and then induces mitochondrial ROS (mtROS) production (2). Increased mtROS leads to PERK activation in the mitochondria-associated membrane (MAM) (3). The phosphorylation of PERK by mtROS increases intracellular calcium concentration. The activation of calcineurin by increased [Ca2 + ]i causes dephosphorylation of TREB (4), followed by its translocation into the nucleus. The nuclear translocation of TFEB increases the expression of genes involved in mitophagy (5) and mitochondrial biogenesis (6) Image collected and cropped by CiteAb from the following open publication (//pubmed.ncbi.nlm.nih.gov/30333475), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb100-304_rabbit-polyclonal-53bp1-antibody-2322024884423.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody [NB100-305] - NIH3T3 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.5% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti- NB100-305 at 2 ug/mL overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:1000 dilution for 60 minutes. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse DyLight 550 (Red) at a 1:1000 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunocytochemistry-Immunofluorescence-NB100-305-img0010.jpg "Immunocytochemistry/Immunofluorescence: 53BP1 Antibody [NB100-305] - NIH3T3 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.5% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti- NB100-305 at 2 ug/mL overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:1000 dilution for 60 minutes. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse DyLight 550 (Red) at a 1:1000 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.")
![<b>Genetic Strategies Validation. </b>Knockdown Validated: 53BP1 Antibody [NB100-305] - Western blot showing an efficient siRNA-mediated knockdown of the indicated individual or combined proteins. Image collected and cropped by CiteAb from the following publication (//www.oncotarget.com/lookup/doi/10.18632/oncotarget.11023) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/53BP1-Antibody-Knockdown-Validated-NB100-305-img0013.jpg)
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-305] - 53BP1 Antibody [NB100-305] - Exosomes modulate the repair of DNA DSBs in irradiated recipient cells. Representative images of 53BP1 foci in BHY cells 6 hours after 2 Gy and transfer of BHY exosomes isolated 24 hours after irradiation with 0, 3, 6 or 9 Gy (53BP1 foci green, nuclei blue). Image collected and cropped by CiteAb from the following publication (//dx.plos.org/10.1371/journal.pone.0152213), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunocytochemistry-Immunofluorescence-NB100-305-img0008.jpg)
![Immunohistochemistry: 53BP1 Antibody [NB100-305] - Immunohistochemical staining of placental villi with 53BP1 Antibody (Catalog #NB100-305) at 40X magnification.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunohistochemistry-NB100-305-img0005.jpg)
![Western Blot: 53BP1 Antibody [NB100-305] - Western blot of whole cell lysate (20 ug/lane) from U2Os cells resolved on a 3 to 8 percent trisacetate gel. A band appears at approximately the theoretical molecular weight of 214 kDa.](http://images.novusbio.com/fullsize/53BP1-Antibody-Western-Blot-NB100-305-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody [NB100-305] - HCC1937 cells (human) were treated with PARPi for 96 h. Nuclei are stained in blue (DAPI) and 53BP1 antibody (foci in green). ICC/IF image submitted by a verified customer review.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunocytochemistry-Immunofluorescence-NB100-305-img0012.jpg)
![Flow Cytometry: 53BP1 Antibody [NB100-305] - An intracellular stain was performed on Ntera2 cells with 53BP1 Antibody NB100-305 (blue) and a matched isotype control NBP2-24891 (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 1.0 ug/mL for 30 minutes at room temperature, followed by Rabbit IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550 (SA5-10033, Thermo Fisher).](http://images.novusbio.com/fullsize/53BP1-Antibody-Flow-Cytometry-NB100-305-img0011.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody [NB100-305] - Paraformaldehyde (4%) fixed Saos-2 cells (human osteosarcoma cell line) were stained with anti-53BP1 antibody followed by Alexa Fluor 488 secondary antibody. ICC/IF image submitted by a verified customer review.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunocytochemistry-Immunofluorescence-NB100-305-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody [NB100-305] - Ntera2 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.5% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti- NB100-305 at 2 ug/mL overnight at 4C and detected with an anti-rabbit DyLight 488 (Green) at a 1:1000 dilution for 60 minutes. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse DyLight 550 (Red) at a 1:1000 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/53BP1-Antibody-Immunocytochemistry-Immunofluorescence-NB100-305-img0009.jpg)
![Flow Cytometry: 53BP1 Antibody [NB100-305] - An intracellular stain was performed on HeLa cells with 53BP1 Antibody (Catalog #NB100-305AF488) (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 488.](http://images.novusbio.com/fullsize/53BP1-Antibody-Flow-Cytometry-NB100-305-img0006.jpg)
![RAP1 protects telomeres against DNA damageWestern blotting showing the expression of RAP1 and TRF2 in MRC-5 cells of different population doublings (PD). Senescent cells (PD 72) were left in culture for at least 4 weeks before harvesting for analysis.ChIP analysis of young (PD 30) and senescent (PD 72) MRC-5 cells performed with either anti-RAP1, anti-TRF2, or an IgG antibody. The immunoprecipitated and input products were loaded into a slot blot membrane and hybridized with a telomere probe, and stripped and hybridized to an Alu probe in order to determine unspecific binding. Quantification was performed by normalizing the telomere signal of the immunoprecipitated to that of the input. Data represent mean +/- SD of three biological replicates.Immunofluorescence detection of 53BP1 (red) and a FISH probe staining telomeres (green) in young (PD 26), pre-senescent (PD 66), and senescent (PD 72 + 4 weeks) MRC-5 fibroblasts. The upper graph shows the percentage of telomere co-localizing with 53BP1 (TIFs). Total DNA damage was measured by immunofluorescence detection of 53BP1. The lower graph shows the total number of 53BP1 foci per nucleus. Approximately 40-50 cells were analyzed per replicate and per condition. Bars represent SEM of two biological replicates.Data information: Statistical analyses were performed using Mann-Whitney U-test (*P 0.05, n = 18; group (mean % of cells with more than five 53BP1 ionizing radiation-induced foci +/−SE); unpaired t test]. See text for details. (C) 53BP1 accumulates at infrequent endogenous chromosomal breaks (indicated by asterisks; no ionizing radiation treatment) in presence or absence of TPX2. (D) Cell cycle profiles of control and TPX2 miRNA expressing HeLa cell cultures obtained via flow cytometry (n = 2). Note that the slight ∼5% increase in the G2/M fraction upon TPX2 depletion can not account for the defect in 53BP1 ionizing radiation-induced foci formation exhibited by ∼55% of TPX2 miRNA expressing cells. See text for details. Error bars represent SE in (B) and SDEV in (D). n = # of independent experiments; NS: non-significant, * p<0.05, ** p<0.01, *** p<0.001; IR: ionizing radiation. Image collected and cropped by CiteAb from the following open publication (//dx.plos.org/10.1371/journal.pone.0110994), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb100-305_rabbit-polyclonal-53bp1-antibody-23220248272420.jpg)
![Western Blot: 53BP1 Antibody - BSA Free [NB100-904] - WRAP53beta plays an important role in recruitment of factors involved in HR and NHEJ to DNA breaks in A2780 cells. A2780 cells were transfected with siControl or siWRAP53#2 oligonucleotides for 48 h; exposed to IR (6 Gy), and 1 h later immunostained for WRAP53beta, gamma-H2AX, MDC1, RNF168, 53BP1, RAD51 and beta-actin. We could not assess the protein levels of BRCA1 due to a lack of antibodies that work for western blotting. The observed molecular weight is 275 kDa and the theoretical molecular weight for the whole endogenous protein is 214 kDa. Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2015250) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Western-Blot-NB100-904-img0015.jpg "Western Blot: 53BP1 Antibody - BSA Free [NB100-904] - WRAP53beta plays an important role in recruitment of factors involved in HR and NHEJ to DNA breaks in A2780 cells. A2780 cells were transfected with siControl or siWRAP53#2 oligonucleotides for 48 h; exposed to IR (6 Gy), and 1 h later immunostained for WRAP53beta, gamma-H2AX, MDC1, RNF168, 53BP1, RAD51 and beta-actin. We could not assess the protein levels of BRCA1 due to a lack of antibodies that work for western blotting. The observed molecular weight is 275 kDa and the theoretical molecular weight for the whole endogenous protein is 214 kDa. Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2015250) licensed under a CC-BY license.")
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - NIH3T3 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.5% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti- NB100-904 at 2 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse Dylight 550 (Red) at a 1:1000 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0021.jpg)
![Immunohistochemistry: 53BP1 Antibody - BSA Free [NB100-904] - Staining of 53BP1 in human renal cancer cells using DAB with hematoxylin counterstain.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunohistochemistry-NB100-904-img0008.jpg)
![Flow Cytometry: 53BP1 Antibody - BSA Free [NB100-904] - An intracellular stain was performed on Ntera2 cells with 53BP1 Antibody NB100-904 (blue) and a matched isotype control NBP2-24891 (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 1.0 ug/mL for 30 minutes at room temperature, followed by Rabbit IgG (H+L) Cross-Adsorbed Secondary Antibody, Dylight 550 (SA5-10033, Thermo Fisher).](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Flow-Cytometry-NB100-904-img0022.jpg)
![Western Blot: 53BP1 Antibody - BSA Free [NB100-904] - Western blot analysis of untreated U2OS cell lysate blotted with 53BP1 Antibody. The observed molecular weight here is ~220 kDa, and the theoretical molecular weight is 214 kDa.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Western-Blot-NB100-904-img0011.jpg)
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - AR suppression treatment suppresses DNA damage repair. (A) Cells were treated with AR suppression for 24 h followed by 2 Gy of IR treatment. Representative images of phospho-H2A histone family member X ( -H2AX) and p53-binding protein 1 (53BP1) staining 24 h post-IR of LNCaP cells (scale bar 10 um). Image collected and cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31635359/) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/53BP1 Antibody - BSA Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0023.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - Immunofluorescence of 53BP1 Antibody in HeLa cells. Image from verified customer review.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - Immunofluorescence of 53BP1 Antibody in C33A cells. Image from verified customer review.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0012.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X PBS + 0.5% Triton X-100. The cells were incubated with 53BP1 Antibody conjugated to Alexa Fluor 488 (Catalog #NB100-904AF488) at 10ug/mL for 1 hour at room temperature. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0013.jpg)
![Immunocytochemistry/Immunofluorescence: 53BP1 Antibody - BSA Free [NB100-904] - Ntera2 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.5% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti-53BP1 Antibody NB100-904 at 2 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Alpha tubulin (DM1A) NB100-690 was used as a co-stain at a 1:1000 dilution and detected with an anti-mouse Dylight 550 (Red) at a 1:1000 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NB100-904-img0019.jpg)
![Flow Cytometry: 53BP1 Antibody - BSA Free [NB100-904] - An intracellular stain was performed on HeLa cells (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to DyLight 550.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Flow-Cytometry-NB100-904-img0014.jpg)
![Flow Cytometry: 53BP1 Antibody - BSA Free [NB100-904] - An intracellular stain was performed on HeLa cells with 53BP1 Antibody (Catalog #NB100-904AF647) (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 2.5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Flow-Cytometry-NB100-904-img0017.jpg)
![Flow Cytometry: 53BP1 Antibody - BSA Free [NB100-904] - An intracellular stain was performed on HeLa cells with 53BP1 Antibody (Catalog #NB100-904C) (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 2.5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to DyLight 650.](http://images.novusbio.com/fullsize/53BP1-Antibody---BSA-Free-Flow-Cytometry-NB100-904-img0018.jpg)
![Western Blot: HDAC9 Antibody [NBP2-03993] - Analysis of HDAC-9 in human HeLa cell lysate in the 1) absence and 2) presence of immunizing peptide and 3) and mouse RAW cell lysate using this antibody. 0 ug/ml, 1.0 ug/ml and 0.5 ug/ml respectively. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/HDAC9-Antibody-Western-Blot-NBP2-03993-img0004.jpg "Western Blot: HDAC9 Antibody [NBP2-03993] - Analysis of HDAC-9 in human HeLa cell lysate in the 1) absence and 2) presence of immunizing peptide and 3) and mouse RAW cell lysate using this antibody. 0 ug/ml, 1.0 ug/ml and 0.5 ug/ml respectively. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.")
![Western Blot: IFI16 Antibody [NBP3-18336] - Western Blot Validation in Rat Testis. Loading: 15 ug of lysate per lane. Antibodies: IFI16 NBP3-18336, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/IFI16-Antibody-Western-Blot-NBP3-18336-img0003.jpg "Western Blot: IFI16 Antibody [NBP3-18336] - Western Blot Validation in Rat Testis. Loading: 15 ug of lysate per lane. Antibodies: IFI16 NBP3-18336, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: IFI16 Antibody [NBP3-18336] - Immunofluorescent analysis of 4% paraformaldehyde-fixed Molt4 cells labeling IFI16 with NBP3-18336 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/IFI16-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18336-img0004.jpg)
![Immunohistochemistry-Paraffin: IFI16 Antibody [NBP3-18336] - Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-IFI16 antibody (NBP3-18336) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/IFI16-Antibody-Immunohistochemistry-Paraffin-NBP3-18336-img0007.jpg)
![Western Blot: IFI16 Antibody [NBP3-18336] - WB Validation in Human and Rat Cell Lines. Loading: 15 ug of lysate per lane. Antibodies: IFI16 NBP3-18336, 2 ug/mL, 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/IFI16-Antibody-Western-Blot-NBP3-18336-img0001.jpg)
![Western Blot: IFI16 Antibody [NBP3-18336] - Western Blot Validation in Mouse Tissues. Loading: 15 ug of lysates per lane. Antibodies: IFI16 NBP3-18336, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/IFI16-Antibody-Western-Blot-NBP3-18336-img0002.jpg)
![Immunohistochemistry-Paraffin: IFI16 Antibody [NBP3-18336] - Immunohistochemical analysis of paraffin-embedded human testis tissue using anti-IFI16 antibody (NBP3-18336) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/IFI16-Antibody-Immunohistochemistry-Paraffin-NBP3-18336-img0005.jpg)
![Immunohistochemistry-Paraffin: IFI16 Antibody [NBP3-18336] - Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-IFI16 antibody (NBP3-18336) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/IFI16-Antibody-Immunohistochemistry-Paraffin-NBP3-18336-img0006.jpg)
![Western Blot: TMEM41B Antibody [NBP3-12858] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12858, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Western-Blot-NBP3-12858-img0007.jpg "Western Blot: TMEM41B Antibody [NBP3-12858] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12858, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: TMEM41B Antibody [NBP3-12858] - Immunofluorescent analysis of 4% paraformaldehyde-fixed HeLa cells labeling TMEM41B with NBP3-12858 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-12858-img0001.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12858] - Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung labeling TMEM41B with NBP3-12858 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12858-img0004.jpg)
![Western Blot: TMEM41B Antibody [NBP3-12858] - WB Validation in Human Cell Lines. Loading: 15 ug of lysate Antibodies: TMEM41B NBP3-12858, 2 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Western-Blot-NBP3-12858-img0005.jpg)
![Western Blot: TMEM41B Antibody [NBP3-12858] - Western Blot Validation in Mouse Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12858, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Western-Blot-NBP3-12858-img0006.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12858] - Immunofluorescent analysis of 4% paraformaldehyde-fixed human colon labeling TMEM41B with NBP3-12858 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12858-img0002.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12858] - Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse kidney labeling TMEM41B with NBP3-12858 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12858-img0003.jpg)
![Western Blot: PEX10 Antibody - BSA Free [NBP3-18137] - WB Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: PEX10 NBP3-18137, 4 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Western-Blot-NBP3-18137-img0003.jpg "Western Blot: PEX10 Antibody - BSA Free [NBP3-18137] - WB Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: PEX10 NBP3-18137, 4 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: PEX10 Antibody - BSA Free [NBP3-18137] - Immunofluorescent analysis of 4% paraformaldehyde-fixed Daudi cells labeling PEX10 with NBP3-18137 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NBP3-18137-img0004.jpg)
![Immunohistochemistry: PEX10 Antibody - BSA Free [NBP3-18137] - Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse thymus labeling PEX10 with NBP3-18137 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Immunohistochemistry-NBP3-18137-img0006.jpg)
![Western Blot: PEX10 Antibody - BSA Free [NBP3-18137] - WB Validation in Human and Mouse Cell Lines. Loading: 15 ug of lysate Antibodies: PEX10 NBP3-18137, 4 ug/mL , 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Western-Blot-NBP3-18137-img0001.jpg)
![Western Blot: PEX10 Antibody - BSA Free [NBP3-18137] - WB Validation in Mouse Tissues. Loading: 15 ug of lysates per lane. Antibodies: PEX10 NBP3-18137, 4 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Western-Blot-NBP3-18137-img0002.jpg)
![Immunohistochemistry: PEX10 Antibody - BSA Free [NBP3-18137] - Immunofluorescent analysis of 4% paraformaldehyde-fixed human spleen labeling PEX10 with NBP3-18137 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/PEX10-Antibody---BSA-Free-Immunohistochemistry-NBP3-18137-img0005.jpg)
![Immunohistochemistry: PEX10 Antibody - BSA Free [NBP3-18137] - Immunofluorescent analysis of 4% paraformaldehyde-fixed rat testis labeling PEX10 with NBP3-18137 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/PEX10 Antibody - BSA Free-Immunohistochemistry-NBP3-18137-img0007.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18133] - WB Validation in Mouse Skeletal Muscle. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18133, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18133-img0007.jpg "Western Blot: AMID Antibody - BSA Free [NBP3-18133] - WB Validation in Mouse Skeletal Muscle. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18133, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: AMID Antibody - BSA Free [NBP3-18133] - Immunofluorescent analysis of 4% paraformaldehyde-fixed HeLa cells labeling AMID with NBP3-18133 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NBP3-18133-img0003.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18133] - Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-AMID antibody (NBP3-18133) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NBP3-18133-img0005.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18133] - WB Validation in Human Mouse and Rat Cell Lines. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18133, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18133-img0001.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18133] - WB Validation in Rat Tissues. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18133, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18133-img0002.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18133] - Immunohistochemical analysis of paraffin-embedded human brain tissue using anti-AMID antibody (NBP3-18133) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NBP3-18133-img0004.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18133] - Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-AMID antibody (NBP3-18133) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID Antibody - BSA Free-Immunohistochemistry-Paraffin-NBP3-18133-img0006.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18132] - WB Validation in Rat Tissues. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18132, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18132-img0003.jpg "Western Blot: AMID Antibody - BSA Free [NBP3-18132] - WB Validation in Rat Tissues. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18132, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: AMID Antibody - BSA Free [NBP3-18132] - Immunofluorescent analysis of 4% paraformaldehyde-fixed HeLa cells labeling AMID with NBP3-18132 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunocytochemistry-Immunofluorescence-NBP3-18132-img0004.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18132] - Immunohistochemical analysis of paraffin-embedded mouse spleen tissue using anti-AMID antibody (NBP3-18132) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NBP3-18132-img0006.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18132] - WB Validation in Human Mouse and Rat Cell Lines. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18132, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18132-img0001.jpg)
![Western Blot: AMID Antibody - BSA Free [NBP3-18132] - WB Validation in Mouse Tissues. Loading: 15 ug of lysate. Antibodies: AMID NBP3-18132, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjuate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Western-Blot-NBP3-18132-img0002.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18132] - Immunohistochemical analysis of paraffin-embedded human testis tissue using anti-AMID antibody (NBP3-18132) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID-Antibody---BSA-Free-Immunohistochemistry-Paraffin-NBP3-18132-img0005.jpg)
![Immunohistochemistry-Paraffin: AMID Antibody - BSA Free [NBP3-18132] - Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-AMID antibody (NBP3-18132) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/AMID Antibody - BSA Free-Immunohistochemistry-Paraffin-NBP3-18132-img0007.jpg)
![Western Blot: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: MCPIP1/ZC3H12A NBP3-18333, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Western-Blot-NBP3-18333-img0003.jpg "Western Blot: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: MCPIP1/ZC3H12A NBP3-18333, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Immunofluorescent analysis of 4% paraformaldehyde-fixed THP-1 cells labeling MCPIP1/ZC3H12A with NBP3-18333 at 10 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18333-img0004.jpg)
![Immunohistochemistry-Paraffin: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-MCPIP1/ZC3H12A antibody (NBP3-18333) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Immunohistochemistry-Paraffin-NBP3-18333-img0007.jpg)
![Western Blot: MCPIP1/ZC3H12A Antibody [NBP3-18333] - WB Validation in Human Lung. Loading: 15 ug of lysate per lane. Antibodies: MCPIP1/ZC3H12A NBP3-18333, 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution. Lane 1: 2 ug/mL Lane 2: 4 ug/mL](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Western-Blot-NBP3-18333-img0001.jpg)
![Western Blot: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Western Blot Validation in Mouse Tissues. Loading: 15 ug of lysates per lane. Antibodies: MCPIP1/ZC3H12A NBP3-18333, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Western-Blot-NBP3-18333-img0002.jpg)
![Immunohistochemistry-Paraffin: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Immunohistochemical analysis of paraffin-embedded human testis tissue using anti-MCPIP1/ZC3H12A antibody (NBP3-18333) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Immunohistochemistry-Paraffin-NBP3-18333-img0005.jpg)
![Immunohistochemistry-Paraffin: MCPIP1/ZC3H12A Antibody [NBP3-18333] - Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-MCPIP1/ZC3H12A antibody (NBP3-18333) at 1 ug/mL. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin](http://images.novusbio.com/fullsize/MCPIP1-ZC3H12A-Antibody-Immunohistochemistry-Paraffin-NBP3-18333-img0006.jpg)
![Western Blot: TMEM41B Antibody [NBP3-12857] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12857, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Western-Blot-NBP3-12857-img0006.jpg "Western Blot: TMEM41B Antibody [NBP3-12857] - Western Blot Validation in Rat Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12857, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: TMEM41B Antibody [NBP3-12857] - Immunofluorescent analysis of 4% paraformaldehyde-fixed HeLa cells labeling TMEM41B with NBP3-12857 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-12857-img0001.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12857] - Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung labeling TMEM41B with NBP3-12857 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12857-img0004.jpg)
![Western Blot: TMEM41B Antibody [NBP3-12857] - Western Blot Validation in Mouse Tissues. Loading: 15 ug of lysates per lane. Antibodies: TMEM41B NBP3-12857, 2 ug/mL, 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Western-Blot-NBP3-12857-img0005.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12857] - Immunofluorescent analysis of 4% paraformaldehyde-fixed human lung labeling TMEM41B with NBP3-12857 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12857-img0002.jpg)
![Immunohistochemistry: TMEM41B Antibody [NBP3-12857] - Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse kidney labeling TMEM41B with NBP3-12857 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/TMEM41B-Antibody-Immunohistochemistry-NBP3-12857-img0003.jpg)
![Western Blot: Frizzled-6 Antibody [NBP3-18335] - WB Validation in Human, Mouse and Rat Cell Lines. Loading: 15 ug of lysate. Antibodies: Frizzled-6 NBP3-18335, 2 ug/mL, 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution.](http://images.novusbio.com/fullsize/Frizzled-6-Antibody-Western-Blot-NBP3-18335-img0001.jpg "Western Blot: Frizzled-6 Antibody [NBP3-18335] - WB Validation in Human, Mouse and Rat Cell Lines. Loading: 15 ug of lysate. Antibodies: Frizzled-6 NBP3-18335, 2 ug/mL, 1 h incubation at RT in 5% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution.")
![Immunocytochemistry/Immunofluorescence: Frizzled-6 Antibody [NBP3-18335] - Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung labeling Frizzled-6 with NBP3-18335 at 10 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/Frizzled-6-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18335-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Frizzled-6 Antibody [NBP3-18335] - Immunofluorescent analysis of 4% paraformaldehyde-fixed Daudi cells labeling Frizzled-6 with NBP3-18335 at 10 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/Frizzled-6-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18335-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Frizzled-6 Antibody [NBP3-18335] - Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse lung labeling Frizzled-6 with NBP3-18335 at 10 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).](http://images.novusbio.com/fullsize/Frizzled-6-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18335-img0003.jpg)