![ICC/IF analysis of Tetrahymena themophila cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. 13C2 mAb was highly specific to the macronucleus. In contrast, in addition to clear macronuclear staining, 21A10 mAb also stained the micronuclear periphery. This indicates that 21A10 mAb recognizes Nups localizing to the micronucleus such as Nup308 in addition to MacNup98A. Neither mABs 2H10 nor 414 could stain nuclear periphery of Tetrahymena. Green : Primary antibody Violet : DAPI Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min ICC/IF analysis of Tetrahymena themophila cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. 13C2 mAb was highly specific to the macronucleus. In contrast, in addition to clear macronuclear staining, 21A10 mAb also stained the micronuclear periphery. This indicates that 21A10 mAb recognizes Nups localizing to the micronucleus such as Nup308 in addition to MacNup98A. Neither mABs 2H10 nor 414 could stain nuclear periphery of Tetrahymena. Green : Primary antibody Violet : DAPI Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_ICC-IF_1_w_23053121_871.webp)
ICC/IF analysis of Tetrahymena themophila cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. 13C2 mAb was highly specific to the macronucleus. In contrast, in addition to clear macronuclear staining, 21A10 mAb also stained the micronuclear periphery. This indicates that 21A10 mAb recognizes Nups localizing to the micronucleus such as Nup308 in addition to MacNup98A. Neither mABs 2H10 nor 414 could stain nuclear periphery of Tetrahymena. Green : Primary antibody Violet : DAPI Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min
NUP98 antibody [21A10]
GTX00695
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
TargetNUP98
Overview
- SupplierGeneTex
- Product NameNUP98 antibody [21A10] - Comparison Validated
- Delivery Days Customer9
- Application Supplier Note*Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID21A10
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID4928
- Target nameNUP98
- Target descriptionnucleoporin 98 and 96 precursor
- Target synonymsADIR2, NUP196, NUP96, Nup98-96, nuclear pore complex protein Nup98-Nup96, nuclear pore complex protein Nup98, GLFG-repeat containing nucleoporin, NUP98/PHF23 fusion 2 protein, Nup98-Nup96, nucleoporin 96, nucleoporin 98kD, nucleoporin 98kDa
- HostMouse
- IsotypeIgG1
- Protein IDP52948
- Protein NameNuclear pore complex protein Nup98-Nup96
- Scientific DescriptionNuclear pore complexes (NPCs) regulate the transport of macromolecules between the nucleus and cytoplasm, and are composed of many polypeptide subunits, many of which belong to the nucleoporin family. This gene belongs to the nucleoporin gene family and encodes a 186 kDa precursor protein that undergoes autoproteolytic cleavage to generate a 98 kDa nucleoporin and 96 kDa nucleoporin. The 98 kDa nucleoporin contains a Gly-Leu-Phe-Gly (GLGF) repeat domain and participates in many cellular processes, including nuclear import, nuclear export, mitotic progression, and regulation of gene expression. The 96 kDa nucleoporin is a scaffold component of the NPC. Proteolytic cleavage is important for targeting of the proteins to the NPC. Translocations between this gene and many other partner genes have been observed in different leukemias. Rearrangements typically result in chimeras with the N-terminal GLGF domain of this gene to the C-terminus of the partner gene. Alternative splicing results in multiple transcript variants encoding different isoforms, at least two of which are proteolytically processed. Some variants lack the region that encodes the 96 kDa nucleoporin. [provided by RefSeq, Feb 2016]
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
References
- Monoclonal antibodies recognize gly-leu-phe-gly repeat of nucleoporin nup98 of tetrahymena, yeasts, and humans. Iwamoto M et al., 2013 Apr, Monoclon Antib Immunodiagn ImmunotherRead more
![ICC/IF analysis of S. pombe cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Green : Primary antibody Violet : DAPI Fixation : 4% PFA for 10 min, treated with 0.6 mg/ml Zymolyase 100T at 3 degree C for 70 min Permeabilization : 1% Triton X-100 for 1 min ICC/IF analysis of S. pombe cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Green : Primary antibody Violet : DAPI Fixation : 4% PFA for 10 min, treated with 0.6 mg/ml Zymolyase 100T at 3 degree C for 70 min Permeabilization : 1% Triton X-100 for 1 min](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_ICC-IF_2_w_23053121_493.webp)
![ICC/IF analysis of S. cereviciae cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Green : Primary antibody Violet : DAPI Dilution : 13C2 or 21A10 : 1:10 2H10 : 10 microg/ml ICC/IF analysis of S. cereviciae cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Green : Primary antibody Violet : DAPI Dilution : 13C2 or 21A10 : 1:10 2H10 : 10 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_ICC-IF_3_w_23053121_421.webp)
![ICC/IF analysis of HeLa cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. The signal at the nuclear periphery with 21A10 mAb was much higher and the background lower than that of 2H10 and 13C2 antibodies. Green : Primary antibody Violet : DAPI Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min ICC/IF analysis of HeLa cells using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. The signal at the nuclear periphery with 21A10 mAb was much higher and the background lower than that of 2H10 and 13C2 antibodies. Green : Primary antibody Violet : DAPI Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_ICC-IF_w_23053121_358.webp)
![Summary of the suitability of GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10] for immunological applications. Summary of the suitability of GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10] for immunological applications.](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_table_1_w_23053121_768.webp)
![WB analysis of Tetrahymena themophila cells or Tetrahymena themophila cells overexpressing GFP-MacNup98A using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Diamonds and asterisks represent uncharacterized proteins. WB analysis of Tetrahymena themophila cells or Tetrahymena themophila cells overexpressing GFP-MacNup98A using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Diamonds and asterisks represent uncharacterized proteins.](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_WB_1_w_23053121_916.webp)
![WB analysis of S. pombe cell l extracts using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Left and right lanes represent specimens from a wild type strain and an S. pombe strain in which Nup98 was chromosomally replaced with Nup98-GFP, respectively. Dilution : 13C2 or 21A10 : 1:10 2H10 : 1 microg/ml WB analysis of S. pombe cell l extracts using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Left and right lanes represent specimens from a wild type strain and an S. pombe strain in which Nup98 was chromosomally replaced with Nup98-GFP, respectively. Dilution : 13C2 or 21A10 : 1:10 2H10 : 1 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_WB_2_w_23053121_268.webp)
![WB analysis of S. cereviciae celll extracts using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Dilution : 13C2 or 21A10 : 1:10 2H10 : 20 microg/ml WB analysis of S. cereviciae celll extracts using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Dilution : 13C2 or 21A10 : 1:10 2H10 : 20 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_WB_3_w_23053121_491.webp)
![WB analysis of HeLa whole cell lysate using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Dilution : 0.4 microg/ml WB analysis of HeLa whole cell lysate using GTX00693 NUP98 antibody [13C2], GTX00695 NUP98 antibody [21A10], or GTX00697 NUP98 antibody [2H10]. Dilution : 0.4 microg/ml](https://www.genetex.com/upload/website/prouct_img/normal/GTX00695/GTX00695_20191104_WB_w_23053121_694.webp)


![ICC/IF analysis of HeLa cells using GTX00697 NUP98 antibody [2H10]. Dilution : 0.5 microg/ml Fixation : Cold Methanol (-30 degree C) for 30 min](https://www.genetex.com/upload/website/prouct_img/normal/GTX00697/GTX00697_20191104_ICC-IF_1_w_23053121_745.webp)



