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rabbit anti tpx2 (Novus Biologicals)

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Novus Biologicals rabbit anti tpx2
Rabbit Anti Tpx2, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+tpx2/TPX2+Antibody/pm41876446-467-4-8
Average 93 stars, based on 47 article reviews

rabbit anti tpx2 - by Bioz Stars, 2026-10

93/100 stars

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Western Blot:

Article Title: A sensitised RNAi screen reveals a ch-TOG genetic interaction network required for spindle assembly
Article Snippet: .. Primary antibodies used for Western blotting are anti-Tpx2 (Novus NB500-179; 1:1000), B-actin (Sigma, AC40; 1:5000), anti-Y-tubulin (Sigma, GTU-88; 1:2000), anti-HSET (Santa Cruz, M-63; 1:1000), anti-ch-TOG (QED Bioscience, 34032, 1:1000). ..

Staining:

Article Title: RAN Nucleo-Cytoplasmic Transport and Mitotic Spindle Assembly Partners XPO7 and TPX2 Are New Prognostic Biomarkers in Serous Epithelial Ovarian Cancer
Article Snippet: .. To unmask antigens, slides were placed for 20 min at high temperature under high pressure in citrate buffer (10 mM sodium citrate, 0.05% Tween 20, pH 6.0) for staining with anti-RCC1 (1/50, SC-1161, Santa Cruz Biotechnology Inc.), anti-IMPβ (1/25, SC-1863, Santa Cruz Biotechnology Inc.) and anti-TPX2 (1/100, NBP1-01041, Novus Biologicals), or in citrate-EDTA buffer (10 mM sodium citrate, 1 mM EDTA, 0.05% Tween 20, pH 8.0) for staining with anti-RANBP1 (1/25, SC-1159, Santa Cruz Biotechnology Inc.), anti-XPOT (1/50, LS-C80366, Lifespan Biosciences Inc.) and anti-XPO7 (1/200, LS-C55360, Lifespan Biosciences Inc.) antibodies. ..

Immunolabeling:

Article Title: Mechanisms underlying disruption of oocyte spindle stability by bisphenol compounds
Article Snippet: .. Oocytes were fixed and immunolabeled with specific antibodies as previously described ( Baumann & Viveiros 2015 ) including, anti-TPX2 (1/500; Novus Biological, Centennial, CO), anti-PCNT (1/1000; BD Biosciences, San Jose, CA or Covance, Princeton, NJ), anti-acetylated α-tubulin (1/1000; Sigma Aldrich) and anti-pT288AURKA (1/1000; Cell Signaling Technology, Beverly, MA). .. In brief, the fixed oocytes were incubated with the primary antibodies overnight at 4°C, then washed and successively incubated (1h) at 37°C with specific Alexa Fluor conjugated 488 or 555 secondary antibodies (Life Technologies, Eugene, OR).

Article Title: Mechanisms underlying disruption of oocyte spindle stability by bisphenol compounds
Article Snippet: .. Immunofluorescence analysis Oocytes were fixed and immunolabeled with specific antibodies as previously described ( Baumann & Viveiros 2015 ) including, anti-TPX2 (1/500; Novus Biological, Centennial, CO), anti-PCNT (1/1000; BD Biosciences, San Jose, CA or Covance, Princeton, NJ), anti-acetylated α-tubulin (1/1000; Sigma Aldrich) and anti-pT288AURKA (1/1000; Cell Signaling Technology, Beverly, MA). .. In brief, the fixed oocytes were incubated with the primary antibodies overnight at 4°C, then washed and successively incubated (1h) at 37°C with specific Alexa Fluor conjugated 488 or 555 secondary antibodies (Life Technologies, Eugene, OR).

Immunofluorescence:

Incubation:

Article Title: A single starfish Aurora kinase performs the combined functions of Aurora-A and Aurora-B in human cells.
Article Snippet: .. The lysate was incubated with protein A–Sepharose conjugated with antiFLAG (M2, Sigma-Aldrich), anti-TPX2 (Novus Biologicals), or anti-INCENP (gift from Jan-Michael Peters, Research Institute of Molecular Pathology, Vienna, Austria) for 1 hour at 4°C. ..

Image Search Results

SVs disrupt gene expression in UTUC. A. Variant Manhattan plot showing genes whose expression is significantly correlated with the proximity of SSV breakpoints. The upper panel displays the number of samples with SSV breakpoints near each gene (y-axis) across the genome (x-axis). Labelled genes indicate significant SSV-expression associations. The lower panel presents genome-wide CNV G-scores for comparison. B. Bar plots quantifying the number of genes with SSV-associated expression changes, before and after adjusting for CNV effects. The reduction in significant associations after adjustment highlights SSVs with independent effects on gene expression. C. Pie charts illustrating the distribution of SSV types among expression-altering breakpoints (left), and the genomic distribution of DEL breakpoints (right), emphasising the prevalence of intronic deletions in gene expression regulation. D. Pie chart showing the proportion of expression-altering SSV breakpoints that are associated with ecDNA. E. Bar plot showing 14 genes with significantly higher SSV frequency in MI-UTUC than in NMI-UTUC (Fisher's exact test). The number of samples with SSVs in each gene is shown for both MI and NMI groups. F. Upper panel: Receiver operating characteristic curves evaluating the predictive performance of TPX2 SSV status for UTUC. AUC values and corresponding p-values are indicated. Lower panel: Box plots showing expression levels of TPX2 in patients with and without SSVs. G. Expression levels of TPX2 in MI and NMI groups across UTUC transcriptomic datasets from published data (BCM, MAD, WCM). H. Representative images of IHC in UTUC samples with TPX2 related SSV (left panel), without TPX2 SSVs (middel panel). Scale bar, 500 μm (left), 100 μm (right). Right panel: A semi-quantitative modified IHC score was calculated in IHC of TPX2 as staining intensity (0–3) × staining extent (0–3), yielding a score range of 0–9. Each dot represents one case; boxes indicate the median and interquartile range.

Journal: eBioMedicine

Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

doi: 10.1016/j.ebiom.2026.106182

Figure Lengend Snippet: SVs disrupt gene expression in UTUC. A. Variant Manhattan plot showing genes whose expression is significantly correlated with the proximity of SSV breakpoints. The upper panel displays the number of samples with SSV breakpoints near each gene (y-axis) across the genome (x-axis). Labelled genes indicate significant SSV-expression associations. The lower panel presents genome-wide CNV G-scores for comparison. B. Bar plots quantifying the number of genes with SSV-associated expression changes, before and after adjusting for CNV effects. The reduction in significant associations after adjustment highlights SSVs with independent effects on gene expression. C. Pie charts illustrating the distribution of SSV types among expression-altering breakpoints (left), and the genomic distribution of DEL breakpoints (right), emphasising the prevalence of intronic deletions in gene expression regulation. D. Pie chart showing the proportion of expression-altering SSV breakpoints that are associated with ecDNA. E. Bar plot showing 14 genes with significantly higher SSV frequency in MI-UTUC than in NMI-UTUC (Fisher's exact test). The number of samples with SSVs in each gene is shown for both MI and NMI groups. F. Upper panel: Receiver operating characteristic curves evaluating the predictive performance of TPX2 SSV status for UTUC. AUC values and corresponding p-values are indicated. Lower panel: Box plots showing expression levels of TPX2 in patients with and without SSVs. G. Expression levels of TPX2 in MI and NMI groups across UTUC transcriptomic datasets from published data (BCM, MAD, WCM). H. Representative images of IHC in UTUC samples with TPX2 related SSV (left panel), without TPX2 SSVs (middel panel). Scale bar, 500 μm (left), 100 μm (right). Right panel: A semi-quantitative modified IHC score was calculated in IHC of TPX2 as staining intensity (0–3) × staining extent (0–3), yielding a score range of 0–9. Each dot represents one case; boxes indicate the median and interquartile range.

Article Snippet: For immunohistochemistry, TPX2 was detected using a rabbit polyclonal anti-TPX2 antibody (HUABIO, ER65201; RRID Tags AB_3731329), generated against a synthesised peptide derived from human TPX2 (aa 301–350), and recommended for IHC-P (1:100–1:300).

Techniques: Gene Expression, Variant Assay, Expressing, Genome Wide, Comparison, Modification, Staining

An upstream structural variant interval enhances TPX2 expression and promotes invasive phenotypes in urothelial cancer cells. A. Schematic representation of somatic structural variants (SSVs) surrounding the TPX2 locus. A recurrent duplication event localised to the chr20:31000852–31001508 interval upstream of TPX2 was identified. This region contains eight tandem repeats of a 171-bp sequence. Two unique sgRNAs were designed to delete a 683-bp fragment spanning this interval. B. PCR and gel electrophoresis validation of CRISPR ribonucleoprotein (RNP)-mediated deletion of the TPX2 upstream interval in 5637 cells. The main band corresponding to the intact region (1025 bp) was markedly attenuated in TPX2-upstream knockout cells. (C, D). Quantitative RT-PCR (C) and Western blot (D) analyses showing that deletion of the chr20:31000852–31001508 interval significantly reduced TPX2 mRNA and protein expression in 5637 cells. (E, F) Quantitative RT-PCR (E) and Western blot (F) analyses demonstrating that transfection of a PCR-derived fragment corresponding to the TPX2 upstream interval increased TPX2 expression compared with control cells. G. Schematic of the dual-luciferase reporter construct in which the TPX2 promoter region (2331 bp, including exon 1) was cloned upstream of the Renilla luciferase (Rluc) gene in the psiCHECK-2 vector. H. Dual-luciferase reporter assay showing that co-transfection of the TPX2 promoter reporter with PCR-derived fragments from the chr20:31000852–31001508 interval significantly increased Rluc activity compared with co-transfection with a random 1-kb DNA fragment, indicating enhancer-like activity of this interval. (I, J) Western blot validation of TPX2 knockout (KO) (I) and TPX2 overexpression (OE) (J) in 5637 cells. (K, L) Wound-healing (K) and transwell migration and invasion assays (L) demonstrating that TPX2 knockout significantly impaired cell motility and invasive capacity. Scale bar = 1 mm in K, scale bar = 200 um in L. (M, N) Wound-healing (M) and transwell migration and invasion assays (N) showing that TPX2 overexpression markedly enhanced migratory and invasive properties of 5637 cells. Scale bar = 1 mm in M, scale bar = 200 um in N. Data are presented as mean ±SD (n = 3). Two-sided Mann-Whitney U test was used for comparisons between two groups. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001). O. KEGG pathway enrichment analysis of genes downregulated upon TPX2 knockout (TPX2_KO vs. NC_KO). P. Gene set enrichment analysis (GSEA) of transcriptomic changes induced by amplification of the TPX2 upstream interval (Ups_OE vs. NC_OE). Pathways related to EMT, cell adhesion, and extracellular matrix remodelling were significantly enriched.

Journal: eBioMedicine

Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

doi: 10.1016/j.ebiom.2026.106182

Figure Lengend Snippet: An upstream structural variant interval enhances TPX2 expression and promotes invasive phenotypes in urothelial cancer cells. A. Schematic representation of somatic structural variants (SSVs) surrounding the TPX2 locus. A recurrent duplication event localised to the chr20:31000852–31001508 interval upstream of TPX2 was identified. This region contains eight tandem repeats of a 171-bp sequence. Two unique sgRNAs were designed to delete a 683-bp fragment spanning this interval. B. PCR and gel electrophoresis validation of CRISPR ribonucleoprotein (RNP)-mediated deletion of the TPX2 upstream interval in 5637 cells. The main band corresponding to the intact region (1025 bp) was markedly attenuated in TPX2-upstream knockout cells. (C, D). Quantitative RT-PCR (C) and Western blot (D) analyses showing that deletion of the chr20:31000852–31001508 interval significantly reduced TPX2 mRNA and protein expression in 5637 cells. (E, F) Quantitative RT-PCR (E) and Western blot (F) analyses demonstrating that transfection of a PCR-derived fragment corresponding to the TPX2 upstream interval increased TPX2 expression compared with control cells. G. Schematic of the dual-luciferase reporter construct in which the TPX2 promoter region (2331 bp, including exon 1) was cloned upstream of the Renilla luciferase (Rluc) gene in the psiCHECK-2 vector. H. Dual-luciferase reporter assay showing that co-transfection of the TPX2 promoter reporter with PCR-derived fragments from the chr20:31000852–31001508 interval significantly increased Rluc activity compared with co-transfection with a random 1-kb DNA fragment, indicating enhancer-like activity of this interval. (I, J) Western blot validation of TPX2 knockout (KO) (I) and TPX2 overexpression (OE) (J) in 5637 cells. (K, L) Wound-healing (K) and transwell migration and invasion assays (L) demonstrating that TPX2 knockout significantly impaired cell motility and invasive capacity. Scale bar = 1 mm in K, scale bar = 200 um in L. (M, N) Wound-healing (M) and transwell migration and invasion assays (N) showing that TPX2 overexpression markedly enhanced migratory and invasive properties of 5637 cells. Scale bar = 1 mm in M, scale bar = 200 um in N. Data are presented as mean ±SD (n = 3). Two-sided Mann-Whitney U test was used for comparisons between two groups. ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001). O. KEGG pathway enrichment analysis of genes downregulated upon TPX2 knockout (TPX2_KO vs. NC_KO). P. Gene set enrichment analysis (GSEA) of transcriptomic changes induced by amplification of the TPX2 upstream interval (Ups_OE vs. NC_OE). Pathways related to EMT, cell adhesion, and extracellular matrix remodelling were significantly enriched.

Techniques: Variant Assay, Expressing, Sequencing, Nucleic Acid Electrophoresis, Biomarker Discovery, CRISPR, Knock-Out, Quantitative RT-PCR, Western Blot, Transfection, Derivative Assay, Control, Luciferase, Construct, Clone Assay, Plasmid Preparation, Reporter Assay, Cotransfection, Activity Assay, Over Expression, Migration, MANN-WHITNEY, Amplification

scRNA-seq reveals TPX2 e xpression in proliferative tumour cell populations and associated pathways. A. UMAP visualisation of single-cell transcriptomic data from UTUC, identifying 20 distinct cell clusters. B. UMAP plot highlighting TPX2 expression, showing enrichment in cycling T cells, cycling epithelial cells, and cycling macrophages. Colour intensity corresponds to TPX2 expression levels. C. Dot plot displaying the percentage of cells expressing TPX2 (dot size) and the average TPX2 expression level (dot colour) across different cell types in patients with MI-UTUC and NMI-UTUC. Asterisks indicate statistically significant differences in expression between MI and NMI for specific cell types (two-sided Wilcoxon rank-sum test, Bonferroni-adjusted P values, ∗P < 0.05, ∗∗∗∗P < 0.001). D. KEGG pathway enrichment analysis of genes significantly upregulated in TPX2 -positive cycling epithelial cells compared with TPX2 -negative counterparts. Dot size represents the number of genes in each pathway; colour indicates the adjusted p-value of enrichment. E. Cell–cell communication heatmap showing the number of predicted ligand-receptor interactions among major cell types in the UTUC tumour microenvironment. Cell types are arranged on both axes, with senders (ligand-expressing cells) on the y-axis and receivers (receptor-expressing cells) on the x-axis. The intensity of red reflects the total number of interactions between each cell pair, as indicated by the colour scale. (F, G) Outgoing (F) and incoming (G) signalling patterns among cell types in the UTUC tumour microenvironment. Heatmaps show the relative strength of ligand-receptor signalling pathways based on CellChat analysis. Colour intensity indicates relative communication strength; bar plots on the top and right summarise overall pathway activity across cell types.

Journal: eBioMedicine

Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

doi: 10.1016/j.ebiom.2026.106182

Figure Lengend Snippet: scRNA-seq reveals TPX2 e xpression in proliferative tumour cell populations and associated pathways. A. UMAP visualisation of single-cell transcriptomic data from UTUC, identifying 20 distinct cell clusters. B. UMAP plot highlighting TPX2 expression, showing enrichment in cycling T cells, cycling epithelial cells, and cycling macrophages. Colour intensity corresponds to TPX2 expression levels. C. Dot plot displaying the percentage of cells expressing TPX2 (dot size) and the average TPX2 expression level (dot colour) across different cell types in patients with MI-UTUC and NMI-UTUC. Asterisks indicate statistically significant differences in expression between MI and NMI for specific cell types (two-sided Wilcoxon rank-sum test, Bonferroni-adjusted P values, ∗P < 0.05, ∗∗∗∗P < 0.001). D. KEGG pathway enrichment analysis of genes significantly upregulated in TPX2 -positive cycling epithelial cells compared with TPX2 -negative counterparts. Dot size represents the number of genes in each pathway; colour indicates the adjusted p-value of enrichment. E. Cell–cell communication heatmap showing the number of predicted ligand-receptor interactions among major cell types in the UTUC tumour microenvironment. Cell types are arranged on both axes, with senders (ligand-expressing cells) on the y-axis and receivers (receptor-expressing cells) on the x-axis. The intensity of red reflects the total number of interactions between each cell pair, as indicated by the colour scale. (F, G) Outgoing (F) and incoming (G) signalling patterns among cell types in the UTUC tumour microenvironment. Heatmaps show the relative strength of ligand-receptor signalling pathways based on CellChat analysis. Colour intensity indicates relative communication strength; bar plots on the top and right summarise overall pathway activity across cell types.

Techniques: Single Cell, Expressing, Activity Assay

Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.

Journal: eBioMedicine

Article Title: Somatic structural variants drive upper tract urothelial carcinoma muscle invasiveness via activation of TPX2 transcription

doi: 10.1016/j.ebiom.2026.106182

Figure Lengend Snippet: Spatial transcriptomic delineation of TPX2 positive epithelial cells and their tumour microenvironmental interactions in UTUC. A. Representative haematoxylin and eosin (H&E)-stained sections (left) and corresponding spatial transcriptomic cell-type annotations (right) from MI (upper) and NMI (lower)-UTUC biopsy, scale bar = 1 mm. Spatial spots were annotated by integrating spatial transcriptomics with single-cell reference datasets, revealing the spatial organisation of epithelial tumour populations and diverse TME components. B. Box plots showing TPX2 expression levels across major spatially defined cell types in MI-UTUC biopsy. TPX2 expression was significantly enriched in basal epithelial tumour cells and specific urothelial tumour subpopulations compared with immune and stromal compartments (∗∗∗∗, P < 0.0001; Wilcoxon rank-sum test). C. Bar plot comparing the proportion of TPX2 positive spots across spatial cell types between MI- and NMI-UTUC samples. TPX2 positive epithelial tumour populations were markedly enriched in MI-UTUC relative to NMI-UTUC. D. Box plots showing average epithelial mesenchymal transition (EMT) signature scores in spatial neighbours of TPX2 positive versus TPX2 negative epithelial tumour cells. Neighbourhoods surrounding TPX2 positive cells exhibited significantly higher EMT associated transcriptional activity (P = 3.33 × 10 −3 ; Wilcoxon rank-sum test), indicating localisation of TPX2 positive tumour cells within invasion-promoting microenvironments. E. Bar plot showing log2 fold changes of EGFR- and EPHA2-associated ligand expression in spatial neighbours of TPX2 positive compared with TPX2 negative epithelial tumour cells.

Techniques: Staining, Spatial Transcriptomics, Single Cell, Expressing, Activity Assay

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rabbit anti tpx2 (Novus Biologicals)

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