Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Other assay [2]
Submit
Validation data
Reference
Comment
Report error
- Product number
- PA5-71284 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- WWC2 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- This target displays homology in the following species: Cow: 92%; Dog: 100%; Guinea Pig: 92%; Horse: 93%; Human: 100%; Mouse: 92%; Pig: 100%; Rat: 92%; Yeast: 83%
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 0.5 mg/mL
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references MicroRNA-10a promotes epithelial-to-mesenchymal transition and stemness maintenance of pancreatic cancer stem cells via upregulating the Hippo signaling pathway through WWC2 inhibition.
Wang C, Yin W, Liu H
Journal of cellular biochemistry 2020 Nov;121(11):4505-4521
Journal of cellular biochemistry 2020 Nov;121(11):4505-4521
No comments: Submit comment
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- 5 Figure miR-10a targets WW and C2 domain containing 2 (WWC2) expression. A, Heat map for the top 30 differentially expressed genes in GSE22780 microarray. B, Combination of the results from TargetScan and mirDIP predictions and differentially expressed genes in GSE22780 microarray, and the intersection, WWC2, was found. C, Binding sites of miR-10a and WWC2 predicted on http://34.236.212.39/microrna/home.do . D, Target relation between miR-10a and WWC2 validated by dual luciferase reporter gene assay. E, F, mRNA expression (E) and protein level (F) of WWC2 PANC-1 CSCs following miR-10a intervention detected using RT-qPCR and Western blot analysis, respectively. G, H, mRNA expression (G) and protein levels (H) of WWC2 in PANC-1 CSCs, PAMC-1, and HPDE6-C7 detected using RT-qPCR and Western blot analysis, respectively. Measurement data were expressed as mean +- SD. Differences between every group pair were analyzed using independent samples t test, while differences among multiple groups were analyzed using one-way ANOVA and Tukey's multiple comparison test. *, compared to the control group, P < .05; repetition = 3. ANOVA, analysis of variance; miR-10a, microRNA-10a; mRNA, messenger RNA; RT-qPCR, reverse transcription quantitative polymerase chain reaction; SD, standard derivation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- 6 Figure miR-10a promotes EMT and stemness maintenance of PANC-1 CSCs by inhibiting WWC2 expression. A, Proliferation activity of PANC-1 CSCs detected using EdU assay (x200). B, Invasion and migration abilities of PANC-1 CSCs measured using Transwell assays (x200). C, Tumor formation ability of PANC-1 CSCs detected via self-renewal assay. D, Colony formation ability of PANC-1 CSCs assessed using colony formation assay in soft agar. E, Expression of miR-10a and stem cancer biomarkers (CD44, CD24, EpCAM, Nanog, OCT-4, and SOX-2) in PANC-1 CSCs evaluated using RT-qPCR. F, Protein levels of EMT-related proteins (E-cadherin, N-cadherin, and Vimentin) and stemness-related proteins (CD44, CD24, EpCAM, Nanog, OCT-4, and SOX-2) detected using Western blot analysis. Measurement data were expressed as mean +- SD. Differences between every group pair were analyzed using independent samples t test, while differences among multiple groups were analyzed using one-way ANOVA and Tukey's multiple comparison test. *, compared to the control group, P < .05; repetition = 3. ANOVA, analysis of variance; CSC, cancer stem cell; EdU, 5-ethynyl-2'-deoxyuridine; EMT, epithelial-to-mesenchymal transition; EpCAM, epithelial cellular adhesion molecule; miR-10a, microRNA-10a; OCT-4, octamer-binding transcription factor-4; RT-qPCR, reverse transcription quantitative polymerase chain reaction; SD, standard derivation; SOX-2, SRY-related high-mobility-group (HMG)-box protein-2; WWC2, WW and C2 domain containi