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94
Proteintech fzd7 antibody
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Fzd7 Antibody, supplied by Proteintech, 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/fzd7 antibody/product/Proteintech
Average 94 stars, based on 1 article reviews
fzd7 antibody - by Bioz Stars, 2026-02
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94
Proteintech anti fzd7
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Anti Fzd7, supplied by Proteintech, 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/anti fzd7/product/Proteintech
Average 94 stars, based on 1 article reviews
anti fzd7 - by Bioz Stars, 2026-02
94/100 stars
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94
Proteintech rabbit polyclonal anti fzd7
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Rabbit Polyclonal Anti Fzd7, supplied by Proteintech, 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/rabbit polyclonal anti fzd7/product/Proteintech
Average 94 stars, based on 1 article reviews
rabbit polyclonal anti fzd7 - by Bioz Stars, 2026-02
94/100 stars
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90
Shanghai GenePharma sirna for braf, fzd7
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Sirna For Braf, Fzd7, supplied by Shanghai GenePharma, 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/sirna for braf, fzd7/product/Shanghai GenePharma
Average 90 stars, based on 1 article reviews
sirna for braf, fzd7 - by Bioz Stars, 2026-02
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94
Proteintech human fzd7
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Human Fzd7, supplied by Proteintech, 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/human fzd7/product/Proteintech
Average 94 stars, based on 1 article reviews
human fzd7 - by Bioz Stars, 2026-02
94/100 stars
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94
Proteintech fzd7
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Fzd7, supplied by Proteintech, 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/fzd7/product/Proteintech
Average 94 stars, based on 1 article reviews
fzd7 - by Bioz Stars, 2026-02
94/100 stars
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90
Cell Signaling Technology Inc antibodies anti- fzd7, anti- mica, anti- hif- 1α, anti- cd44 and anti- nk1.1 (cd161)
a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of <t>FZD7</t> expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).
Antibodies Anti Fzd7, Anti Mica, Anti Hif 1α, Anti Cd44 And Anti Nk1.1 (Cd161), supplied by Cell Signaling Technology Inc, 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/antibodies anti- fzd7, anti- mica, anti- hif- 1α, anti- cd44 and anti- nk1.1 (cd161)/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
antibodies anti- fzd7, anti- mica, anti- hif- 1α, anti- cd44 and anti- nk1.1 (cd161) - by Bioz Stars, 2026-02
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94
Proteintech antibody against fzd7
( A , C , E , G , I ) <t>FZD7</t> is significantly up-regulated in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets. ( B , D , F , H , J ) The receiver-operating characteristic (ROC) curve and the area under the curve (AUC) curve of FZD7 in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets.
Antibody Against Fzd7, supplied by Proteintech, 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/antibody against fzd7/product/Proteintech
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antibody against fzd7 - by Bioz Stars, 2026-02
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Image Search Results


a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of FZD7 expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).

Journal: Nature Communications

Article Title: Deep learning-assisted discovery of a potent and cell-active inhibitor of RNA N 6 -methyladenosine recognition protein YTHDC2

doi: 10.1038/s41467-025-65542-0

Figure Lengend Snippet: a Western blot analyses of H3K4me3 expression in DC2-C1 -treated PANC-1 or MiaPACA-2 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . b Quantitative analysis of Western blot for PANC-1 or MiaPACA-2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. c Colony formation assay of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . d Abilities of invasion of PANC-1 or MiaPACA-2 cells treated with DC2-C1 or 16o . Scale bar, 50 μm. e-g ACC1 , FASN and SREBP-1C mRNA expression were determined by RT-qPCR in DC2-C1 -treated HepG2 cells. Data are shown as the mean ± SD from three technical replicates in three independent experiments. h Western blot analyses of ID2 expression in DC2-C1 -treated PANC-1 cells; Western blot analyses of FZD7 expression in DC2-C1 -treated HGC27 cells. Blots shown are representative of three biological replicates. Full blots can be found in Supplementary Fig. . i FZD7 mRNA expression was determined by RT-qPCR in DC2-C1 -treated HGC27 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. j ID2 mRNA expression was validated by RT-qPCR in DC2-C1 -treated PANC-1 cells. Data are shown as the mean ± SD from four technical replicates in four independent experiments. Source data are provided as a Source Data file. (* P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001; by two-tailed unpaired Student's t-test).

Article Snippet: Antibodies used: YTHDC2 antibody (ZenBio, R27443 ), AMIGO2 antibody (ImmunoWay, YN2372), ID2 antibody (HUABIO, M1301-2), H3K4me3 antibody (Abcam, ab8580), FZD7 antibody (Proteintech, 16974-1-AP), DYKDDDDK Tag (Flag-tag) antibody (Cell Signaling Technology, 14793), GAPDH antibody (Proteintech, 60004-1-Ig), HRP-conjugated Affinipure Goat Anti-Rabbit IgG(H + L) (Proteintech, SA00001-2), HRP-conjugated Affinipure Goat Anti-Mouse IgG(H + L) (Proteintech, SA00001-1).

Techniques: Western Blot, Expressing, Colony Assay, Quantitative RT-PCR, Two Tailed Test

( A , C , E , G , I ) FZD7 is significantly up-regulated in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets. ( B , D , F , H , J ) The receiver-operating characteristic (ROC) curve and the area under the curve (AUC) curve of FZD7 in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets.

Journal: Scientific Reports

Article Title: Identification of FZD7 as a potential ferroptosis-related diagnostic gene in endometriosis by bioinformatics analysis

doi: 10.1038/s41598-025-90803-9

Figure Lengend Snippet: ( A , C , E , G , I ) FZD7 is significantly up-regulated in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets. ( B , D , F , H , J ) The receiver-operating characteristic (ROC) curve and the area under the curve (AUC) curve of FZD7 in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets.

Article Snippet: The membrane was blocked with 5% skimmed milk powder solution for 2 h, then incubated with primary antibody against FZD7 (16974-1-AP, Proteintech, China) overnight at 4 °C, followed by incubation with secondary antibody for 2 h at room temperature.

Techniques:

GO and KEGG pathways for the overlapping FZD7 positively associated genes in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets.

Journal: Scientific Reports

Article Title: Identification of FZD7 as a potential ferroptosis-related diagnostic gene in endometriosis by bioinformatics analysis

doi: 10.1038/s41598-025-90803-9

Figure Lengend Snippet: GO and KEGG pathways for the overlapping FZD7 positively associated genes in GSE11691, GSE7305, GSE5108, GSE23339 and GSE25628 datasets.

Article Snippet: The membrane was blocked with 5% skimmed milk powder solution for 2 h, then incubated with primary antibody against FZD7 (16974-1-AP, Proteintech, China) overnight at 4 °C, followed by incubation with secondary antibody for 2 h at room temperature.

Techniques:

( A , C ) The infiltration of 22 immune cells in EMS of GSE11691dataset. ( B ) The relationship between FZD7 and 22 immune cells in GSE11691 dataset. ( D ) The expression of FZD7 in GSE19834. ( E ) Immunofluorescence images staining with CD206 in Vehicle group and F7H group.

Journal: Scientific Reports

Article Title: Identification of FZD7 as a potential ferroptosis-related diagnostic gene in endometriosis by bioinformatics analysis

doi: 10.1038/s41598-025-90803-9

Figure Lengend Snippet: ( A , C ) The infiltration of 22 immune cells in EMS of GSE11691dataset. ( B ) The relationship between FZD7 and 22 immune cells in GSE11691 dataset. ( D ) The expression of FZD7 in GSE19834. ( E ) Immunofluorescence images staining with CD206 in Vehicle group and F7H group.

Article Snippet: The membrane was blocked with 5% skimmed milk powder solution for 2 h, then incubated with primary antibody against FZD7 (16974-1-AP, Proteintech, China) overnight at 4 °C, followed by incubation with secondary antibody for 2 h at room temperature.

Techniques: Expressing, Immunofluorescence, Staining

( A-C ) The expression of FZD7 in ectopic (Ec) endometrial tissues, eutopic (Eu) endometrial tissues and normal endometrial (NE) tissues. ** p < 0.01, *** p < 0.001, ns, no significant difference by one-way analysis of variance (ANOVA) test.

Journal: Scientific Reports

Article Title: Identification of FZD7 as a potential ferroptosis-related diagnostic gene in endometriosis by bioinformatics analysis

doi: 10.1038/s41598-025-90803-9

Figure Lengend Snippet: ( A-C ) The expression of FZD7 in ectopic (Ec) endometrial tissues, eutopic (Eu) endometrial tissues and normal endometrial (NE) tissues. ** p < 0.01, *** p < 0.001, ns, no significant difference by one-way analysis of variance (ANOVA) test.

Article Snippet: The membrane was blocked with 5% skimmed milk powder solution for 2 h, then incubated with primary antibody against FZD7 (16974-1-AP, Proteintech, China) overnight at 4 °C, followed by incubation with secondary antibody for 2 h at room temperature.

Techniques: Expressing