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Bioss
spin4 ![]() Spin4, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/spin4/product/Bioss Average 94 stars, based on 1 article reviews
spin4 - by Bioz Stars,
2026-06
94/100 stars
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World Precision Instruments
4-way stopcock, yellow, 2 female luer locks, male luer with spin lock ![]() 4 Way Stopcock, Yellow, 2 Female Luer Locks, Male Luer With Spin Lock, supplied by World Precision Instruments, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/4-way stopcock, yellow, 2 female luer locks, male luer with spin lock/product/World Precision Instruments Average 93 stars, based on 1 article reviews
4-way stopcock, yellow, 2 female luer locks, male luer with spin lock - by Bioz Stars,
2026-06
93/100 stars
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Santa Cruz Biotechnology
rabbit anti dystrophin ![]() Rabbit Anti Dystrophin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/rabbit anti dystrophin/product/Santa Cruz Biotechnology Average 90 stars, based on 1 article reviews
rabbit anti dystrophin - by Bioz Stars,
2026-06
90/100 stars
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Human SPIN4 Protein Lysate 20ug from Innovative Research is provided as a Lyophilized powder. This is a Recombinant Protein Lysate produced in HEK293T cells. This protein lysate can be reconsituted using SDS Sample Buffer. Once
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SPIN4 (Spindlin Family Member 4) is a Protein Coding gene. An important paralog of this gene is SPIN1. Exhibits H3K4me3-binding activity.
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SPIN4 (Spindlin Family Member 4) is a Protein Coding gene. An important paralog of this gene is SPIN1. Exhibits H3K4me3-binding activity.
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Spin4 Mouse 3 unique 27mer siRNA duplexes 2 nmol each
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Recombinant protein of human spindlin family member 4 SPIN4
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Rabbit polyclonal antibody against SPIN4 conjugated to Biotin. Isotype Note: IgG Host Note: Rabbit Conjugation Note: Biotin Reactivity Note: Human Application Note: ELISA
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Using a secreted and robust Gaussia Luciferase (GLuc) as the reporter, GeneCopoeia GLuc-ON promoter clones are designed for promoter analysis by detecting the real-time activities of about 39,500 human, 28,700 mouse and 17,500 rat promoters
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Rabbit anti-Human SPIN4 Polyclonal Antibody
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Transient overexpression lysate of spindlin family, member 4 (SPIN4)
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Image Search Results
Journal: Oncogenesis
Article Title: Human papillomavirus16 E7 enhances cell stemness by regulating the APC2/SPIN4/β-catenin axis in cervical cancer
doi: 10.1038/s41389-026-00602-8
Figure Lengend Snippet: A Venn diagram showing the overlap of HPV16 E7 silence-related DEGs and TCGA data of APC2-related DEGs in cervical cancer. (B) FPKM value of these overlap genes (** p < 0.01, * p < 0.05). C The bar graph represents the qPCR analysis of these overlap DEG expressions in siR-E7-treated SiHa cells ( n = 3; student’s t -test; ** p < 0.01, * p < 0.05). D WB analysis of SPIN4 expression in Caski and SiHa cells treated with siR-NC or siR-E7 ( n = 3; student’s t -test; ** p < 0.01, * p < 0.05). E Correlation analysis between APC2 and SPIN4 expression in cervical cancer tissues. A scatter plot with the correlation coefficient ( R ) and p -value is shown. F The expression of SPIN4 in clinical samples was detected by IHC assay. (200× and 400× magnification; Scale bar: 100 μm and 50 μm; n = 10; student’s t -test; ** p < 0.01). G The expression of SPIN4 in HPV16 E7-silenced xenograft tumor tissues was detected by IHC assay. (200× and 400× magnification; Scale bar: 100 μm and 50 μm; n = 3; student’s t -test; * p < 0.05). H WB analysis of SPIN4 expression in cervical cancer cells transfected with APC2 overexpression or APC2 silencing ( n = 3; student’s t-test; ** p < 0.01, * p < 0.05).
Article Snippet:
Techniques: Expressing, Transfection, Over Expression
Journal: Oncogenesis
Article Title: Human papillomavirus16 E7 enhances cell stemness by regulating the APC2/SPIN4/β-catenin axis in cervical cancer
doi: 10.1038/s41389-026-00602-8
Figure Lengend Snippet: A Box plot comparing SPIN4 expression levels between adjacent healthy and tumor tissues in cervical cancer patients from the TCGA database. p = 0.027 by the Wilcoxon signed-rank test. B Kaplan–Meier curve illustrating the overall survival of cervical cancer patients stratified by high (blue line) or Low (red line) SPIN4 expression. Using C GO enrichment analysis and D KEGG methods, we evaluated the functional categories and potential signaling pathways enriched by SPIN4-related DEGs. E SiHa cells were transfected with siR-SPIN4 or siR-NC, and the transfection efficiency was examined by WB assay (n = 3; student’s t -test; ** p < 0.01). F Proliferation ability of SiHa cells transfected with pcDNA3.1+siR-NC, APC2+siR-NC, or APC2+siR-SPIN4 was assessed by MTT assay at 0, 24, 48, and 72 h, respectively ( n = 3; ANOVA; ** p < 0.01). G The transwell assay evaluated the impact of APC2 overexpression combined with SPIN4 silencing on SiHa cell migration and invasion, contrasted with control cells. The image was magnified 100× (Scale bar: 100 μm; n = 3; ANOVA; ** p < 0.01, * p < 0.05). H S p here-forming assay showing the effects of SPIN4 silencing on sphere formation in SiHa cells with APC2 overexpression (Scale bar: 50 μm; n = 3; ANOVA; ** p < 0.01). I The protein levels of OCT4, SOX2, Nanog, and β-catenin expressed in SiHa cells that overexpressed APC2 and simultaneously silenced SPIN4 were tested by WB assays ( n = 3; ANOVA; ** p < 0.01, * p < 0.05).
Article Snippet:
Techniques: Expressing, Functional Assay, Protein-Protein interactions, Transfection, MTT Assay, Transwell Assay, Over Expression, Migration, Control
Journal: Oncogenesis
Article Title: Human papillomavirus16 E7 enhances cell stemness by regulating the APC2/SPIN4/β-catenin axis in cervical cancer
doi: 10.1038/s41389-026-00602-8
Figure Lengend Snippet: A Representative images of xenograft tumors harvested from mice injected with SiHa cells stably expressing either non-targeting control shRNA (Lenti-sh-NC) or SPIN4-targeting shRNA (Lenti-sh-SPIN4) ( n = 3). B Mouse body weights were monitored throughout the experiment. C Quantitative analysis of tumor volume and weight ( n = 6; student’s t -test; ** p < 0.01). D IHC staining of xenograft tumor sections for the stemness markers OCT4, SOX2, and Nanog, and the Wnt pathway component β-catenin ( n = 3; student’s t -test; ** p < 0.01).
Article Snippet:
Techniques: Injection, Stable Transfection, Expressing, Control, shRNA, Immunohistochemistry