anti ftl Search Results


polyclonal rabbit anti human 478 jo urn al pr pr oo f 13 ferritin  (Sino Biological)
93
Sino Biological polyclonal rabbit anti human 478 jo urn al pr pr oo f 13 ferritin
Polyclonal Rabbit Anti Human 478 Jo Urn Al Pr Pr Oo F 13 Ferritin, supplied by Sino Biological, 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/product/anti+ftl/FTL+%2F+ferritin%2C+light+polypeptide+Antibody%2C+Rabbit+PAb%2C+Antigen+Affinity+Purified/10__1016_slash_j__isci__2025__113738-227-31-48
Average 93 stars, based on 1 article reviews
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ftl  (NSJ Bioreagents)
90
NSJ Bioreagents ftl
Ftl, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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ftl  (Atlas Antibodies)
88
Atlas Antibodies ftl
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Ftl, supplied by Atlas Antibodies, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ftl/Anti-FTL/pmc06127892-174-48-49
Average 88 stars, based on 1 article reviews
ftl - by Bioz Stars, 2026-10
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anti ferritin light chain ftl polyclonal antibody  (Proteintech)
96
Proteintech anti ferritin light chain ftl polyclonal antibody
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Anti Ferritin Light Chain Ftl Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ftl/Ferritin+light+chain+Antibody/pm41855087-52-0-10
Average 96 stars, based on 1 article reviews
anti ferritin light chain ftl polyclonal antibody - by Bioz Stars, 2026-10
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mouse anti ftl monoclonal antibody  (Chengdu Zen Bioscience)
90
Chengdu Zen Bioscience mouse anti ftl monoclonal antibody
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Mouse Anti Ftl Monoclonal Antibody, supplied by Chengdu Zen Bioscience, 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/product/anti+ftl/mouse+anti+ftl+monoclonal+antibody/pmc11290555-163-50-55
Average 90 stars, based on 1 article reviews
mouse anti ftl monoclonal antibody - by Bioz Stars, 2026-10
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goat anti-ftl abnova pab11455  (Abnova)
90
Abnova goat anti-ftl abnova pab11455
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Goat Anti Ftl Abnova Pab11455, supplied by Abnova, 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/product/anti+ftl/goat+anti+ftl+abnova+pab11455/pm22693571-70-32-34
Average 90 stars, based on 1 article reviews
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mouse anti-ftl monoclonal antibody 220988  (Chengdu Zen Bioscience)
90
Chengdu Zen Bioscience mouse anti-ftl monoclonal antibody 220988
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Mouse Anti Ftl Monoclonal Antibody 220988, supplied by Chengdu Zen Bioscience, 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/product/anti+ftl/mouse+anti+ftl+monoclonal+antibody+220988/pm39083563-159-54-60
Average 90 stars, based on 1 article reviews
mouse anti-ftl monoclonal antibody 220988 - by Bioz Stars, 2026-10
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rabbit polyclonal anti ftl  (Biorbyt)
85
Biorbyt rabbit polyclonal anti ftl
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Rabbit Polyclonal Anti Ftl, supplied by Biorbyt, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ftl/FTL+antibody/pm22103328-96-33-36
Average 85 stars, based on 1 article reviews
rabbit polyclonal anti ftl - by Bioz Stars, 2026-10
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ferritin light chain  (Novus Biologicals)
93
Novus Biologicals ferritin light chain
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Ferritin Light Chain, supplied by Novus Biologicals, 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/product/anti+ftl/Ferritin+Light+Chain+Antibody+(FTL%2F1386)+%5BDyLight+350%5D/pm40571738-594-91-96
Average 93 stars, based on 1 article reviews
ferritin light chain - by Bioz Stars, 2026-10
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ftl  (Huabio Inc)
86
Huabio Inc ftl
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Ftl, supplied by Huabio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ftl/anti+ftl/pmc12796233-74-12-15
Average 86 stars, based on 1 article reviews
ftl - by Bioz Stars, 2026-10
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ftl  (Servicebio Inc)
86
Servicebio Inc ftl
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Ftl, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ftl/anti+ftl/pmc13194551-407-52-56
Average 86 stars, based on 1 article reviews
ftl - by Bioz Stars, 2026-10
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anti ftl  (Abmart Inc)
86
Abmart Inc anti ftl
A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), <t>FTL</t> ( P = 0.0001) (C), LGALS7 ( P = 0.0001) <t>and</t> <t>FAM83H</t> ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.
Anti Ftl, supplied by Abmart Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), FTL ( P = 0.0001) (C), LGALS7 ( P = 0.0001) and FAM83H ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.

Journal: EMBO Molecular Medicine

Article Title: Comparative proteomics reveals a diagnostic signature for pulmonary head‐and‐neck cancer metastasis

doi: 10.15252/emmm.201708428

Figure Lengend Snippet: A Volcano plot relating adjusted p values for differential protein expression to averaged normalised SILAC ratios of two replicates. Red (higher expression in HNSCC) and blue (higher expression in SQCLC) dots indicate significantly regulated proteins ( P < 0.05). B Two‐class comparison of genetic dependencies from a publically available genome‐scale CRISPR‐Cas9 screen of HNSCC (12 cell line) versus SQCLC (10 cell lines) identified a subset of differentially expressed proteins that were also differential dependencies in these tumour types. The x ‐axis represents the effect size of the mean difference of dependency scores in HNSCC compared to SQCLC cell lines. Positive effect size indicates a greater mean dependency in HNSCC; negative effect size indicates a greater mean dependency in SQCLC. The y ‐axis represents the statistical significance of differential enrichment calculated as ‐log10( P ‐value) from a two‐sided t ‐test. The P ‐values used for this plot are uncorrected for multiple hypothesis testing. Highlighted in green are genetic dependencies that were also identified as differentially expressed proteins in our study. C, D Immunohistochemical analysis of the expression of HMGCS‐1 ( P = 0.0014), FTL ( P = 0.0001) (C), LGALS7 ( P = 0.0001) and FAM83H ( P = 0.0001) (D) in an independent cohort of 212 SQCLC and 343 HNSCC cases. Scale bar indicates 100 μm. Shown are mean values and standard deviation. Statistical significance was assessed using Wilcoxon–Mann–Whitney test. E Pathway enrichment analysis for proteins differentially expressed in HNSCC and SQCLC.

Article Snippet: Briefly, 2‐μm tissue sections were incubated in EnVision Flex Target Retrieval Solution, pH high or low (Dako) followed by incubation of primary antibodies against CK5/6 (Dako, prediluted, high), CK7 (Dako, prediluted, high), p63 (Bio‐Genex, prediluted, high), TTF‐1 (Dako, prediluted, high), CD34 (Dako, prediluted, low), CK19 (Dako, prediluted, high), FTL (Atlas antibodies, 1:1,000, high), FAM83H (1:500, low), LGALS7 (Abcam, 1:20,000, high) or HMGCS1 (Atlas antibodies, 1:200, low) at room temperature for 20 min. Polymeric secondary antibodies coupled to HRPO peroxidase (EnVision Flex + , Dako) and DAB (Dako) were applied to visualise the sites of immunoprecipitations.

Techniques: Expressing, Multiplex sample analysis, Comparison, CRISPR, Immunohistochemical staining, Standard Deviation, MANN-WHITNEY