Human ROR2 Antibody

Detection of Human ROR2 by Western Blot.

Western blot shows lysates of HeLa human cervical epithelial carcinoma cell line and T47D human breast cancer cell line. PVDF membrane was probed with 0.1 µg/mL of Goat Anti-Human ROR2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2064) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). A specific band was detected for ROR2 at approximately 105 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.

Detection of Human ROR2 by Simple Western^TM.

Simple Western lane view shows lysates of HeLa human cervical epithelial carcinoma cell line, loaded at 0.2 mg/mL. A specific band was detected for ROR2 at approximately 139 kDa (as indicated) using 10 µg/mL of Goat Anti-Human ROR2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2064) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.

Detection of Human ROR2 by Western Blot

ROR2 negatively regulates the differentiation of hiPSCs into NS/PCs. (a) Microarray data of ROR2 expression in 10 hiPSC lines (n = 6, biological replicates). Using one-way ANOVA, a significant difference in ROR2 expression was observed between cell lines (P < 0.0001). (b) ROR2 KD was confirmed using qRT-PCR analysis (n = 3, biological replicates). (c) Western blotting analysis of the total extracts obtained from control and ROR2 KD cells. beta -actin was used as a loading control. Molecular weight is indicated as Mr (k). (d) qRT-PCR analysis of undifferentiated hPSC markers, OCT3/4 and LIN28A. Total RNA was isolated from R-2A ROR2 KD cells and R-2A control shRNA cells in the undifferentiated state (n = 3, biological replicates). (e, f) qRT-PCR analysis of NS/PC and astrocyte marker genes in NS/PCs derived from ROR2 KD and control shRNA cells (n = 3, biological replicates). Suspension method (e) and adhesion method (f) are shown. (g) Immunofluorescence staining of PAX6 (red) and DAPI (blue) in control (upper) and ROR2 KD (lower) cells. Scale bars, 100 µm. *P < 0.05, **P < 0.01, ****P < 0.0001 (two-tailed unpaired t-test). Error bars represent mean ± SD. Image collected and cropped by CiteAb from the following open publication (https://www.nature.com/articles/s41598-023-51082-4), licensed under a CC-BY license. Not internally tested by R&D Systems.