Review



rabbit anti lifr  (Proteintech)


Bioz Verified Symbol Proteintech is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 92

    Structured Review

    Proteintech rabbit anti lifr
    Rabbit Anti Lifr, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lifr/LIFR+Antibody/pmc12994253-129-35-38
    Average 92 stars, based on 30 article reviews
    rabbit anti lifr - by Bioz Stars, 2026-09
    92/100 stars

    Images

    Related Articles

    Extraction:

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018- 1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018-1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    SDS Page:

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018- 1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018-1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Nucleic Acid Electrophoresis:

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018- 1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018-1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Incubation:

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018- 1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Total protein was extracted with a RIPA extraction reagent (Beyotime, Shanghai, China), and the proteins were separated through 10% SDS-PAGE gel electrophoresis, transferred to PVDF membranes, and blocked with 5% skimmed milk powder on a 37 °C shaker for 1 h, washed three times with TBST buffer, and incubated with primary antibodies E-cadherin (1:2000; 20874-1-AP; Proteintech, Wuhan, China), N-cadherin (1:2000; 22018-1-AP; Proteintech), Vimentin (1:10000; 10366-1-AP; Proteintech), LIFR (1:2000; 22779-1-AP; Proteintech), GAPDH (1:2000; 60004-1-Ig; Proteintech) on a shaker at room temperature for 30 min and overnight at 4 °C. .. Then, the bands were visualized with a chemiluminescence kit (Beyotime, Shanghai, China).

    Article Title: Distinct adipose progenitor cells emerging with age drive active adipogenesis.
    Article Snippet: INTRODUCTION: Adipose tissue plays a crucial role in regulating various hormonal andmetabolic processes and demonstrates substantial compositional and phenotypic plasticity.. From middle age to early aging, adults often experience a notable increase in visceral adipose tissuemass.. Visceral adiposity is believed to be an important risk factor for various metabolic disorders.

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H 2 O 2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.

    Article Title: Genome-wide analysis reveals porcine LIFR regulated by DNA methylation promotes the implantation process via the STAT3 signaling.
    Article Snippet: Embryo-uterine interaction during embryo implantation depends on the coordinated expression of numerous genes in the receptive endometrium.. While DNA methylation is known to play a significant role in controlling gene expression, specific molecular mechanisms underlying this regulatory event remain elusive in early porcine pregnancy.. Here, we investigated the genome-wide DNA methylation landscape in the Yorkshire and Meishan pig’s endometrium.

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H2O2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.

    Immunohistochemistry:

    Article Title: Use of integrated spatial transcriptomics and histopathological analysis in adamantinomatous craniopharyngiomas to identify stromal cells as a new cellular source of leukemia inhibitory factor
    Article Snippet: © 2025 The authors, CC BY-NC-ND 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) ABBREVIATIONS ACP = adamantinomatous craniopharyngioma; AOD = average optical density; DEG = differentially expressed gene; GSEA = Gene Set Enrichment Analysis; H&E = hematoxylin and eosin; IL = interleukin; KEGG = Kyoto Encyclopedia of Genes and Genomes; LIF = leukemia inhibitory factor; LIFR = LIF receptor; OSM = oncostatin M; PE = palisade epithelium; SR = stellate reticulum.. SUBMITTED December 18, 2024.. ACCEPTED April 16, 2025.

    Immunofluorescence:

    Article Title: Use of integrated spatial transcriptomics and histopathological analysis in adamantinomatous craniopharyngiomas to identify stromal cells as a new cellular source of leukemia inhibitory factor
    Article Snippet: © 2025 The authors, CC BY-NC-ND 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) ABBREVIATIONS ACP = adamantinomatous craniopharyngioma; AOD = average optical density; DEG = differentially expressed gene; GSEA = Gene Set Enrichment Analysis; H&E = hematoxylin and eosin; IL = interleukin; KEGG = Kyoto Encyclopedia of Genes and Genomes; LIF = leukemia inhibitory factor; LIFR = LIF receptor; OSM = oncostatin M; PE = palisade epithelium; SR = stellate reticulum.. SUBMITTED December 18, 2024.. ACCEPTED April 16, 2025.

    Staining:

    Article Title: Use of integrated spatial transcriptomics and histopathological analysis in adamantinomatous craniopharyngiomas to identify stromal cells as a new cellular source of leukemia inhibitory factor
    Article Snippet: © 2025 The authors, CC BY-NC-ND 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) ABBREVIATIONS ACP = adamantinomatous craniopharyngioma; AOD = average optical density; DEG = differentially expressed gene; GSEA = Gene Set Enrichment Analysis; H&E = hematoxylin and eosin; IL = interleukin; KEGG = Kyoto Encyclopedia of Genes and Genomes; LIF = leukemia inhibitory factor; LIFR = LIF receptor; OSM = oncostatin M; PE = palisade epithelium; SR = stellate reticulum.. SUBMITTED December 18, 2024.. ACCEPTED April 16, 2025.

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H 2 O 2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H2O2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.

    Activity Assay:

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H 2 O 2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.

    Article Title: miR-196a-5p promotes the proliferation, migration, and invasion of esophageal squamous cell carcinoma by targeting LIFR.
    Article Snippet: .. Endogenous peroxidase activity was blocked with 3% H2O2 for 10 min, and antigenicity was determined after boiling in EDTA buffer (pH = 9) for 20 min. After incubation with bovine serum albumin for 20 min at room temperature, the primary antibody E-cadherin (1:200; 20874-1-AP; Proteintech), Ki67 (1:200; 27309-1-AP; Proteintech), Vimentin (1:200; 10366-1-AP; Proteintech), LIFR (1:200; 22779-1-AP; Proteintech) was incubated overnight at 4, followed by 30 min at room temperature with enzyme-labeled secondary antibodies and stained with DAB. .. All data were statistically analyzed with GraphPad Prism 8.0 software, and results were presented as mean ± standard deviation of at least three independent experiments.



    Similar Products

    95
    Thermo Fisher gene exp lifr mm00442942 m1
    (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of <t>lifr</t> expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.
    Gene Exp Lifr Mm00442942 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lifr/Gene+Exp%2E+Lifr%2C+Mm00442942_m1/bio_rxiv__64898__2026__02__24__707802-252-16--1
    Average 95 stars, based on 1 article reviews
    gene exp lifr mm00442942 m1 - by Bioz Stars, 2026-09
    95/100 stars
      Buy from Supplier

    90
    Sino Biological lifr
    (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of <t>lifr</t> expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.
    Lifr, supplied by Sino Biological, 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/lifr/LIFR+Antibody%2C+Rabbit+PAb%2C+Antigen+Affinity+Purified/pm41543620-82-71-76
    Average 90 stars, based on 1 article reviews
    lifr - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    92
    Proteintech rabbit anti lifr
    (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of <t>lifr</t> expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.
    Rabbit Anti Lifr, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lifr/LIFR+Antibody/pmc12994253-129-35-38
    Average 92 stars, based on 1 article reviews
    rabbit anti lifr - by Bioz Stars, 2026-09
    92/100 stars
      Buy from Supplier

    92
    Proteintech lifr
    (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of <t>lifr</t> expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.
    Lifr, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lifr/LIFR+Antibody/bio_rxiv__64898__2026__02__24__707802-261-10-11
    Average 92 stars, based on 1 article reviews
    lifr - by Bioz Stars, 2026-09
    92/100 stars
      Buy from Supplier

    94
    OriGene lifr expression detection
    Expression validation of <t>LIFR</t> in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing <t>LIFR</t> <t>expression</t> patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.
    Lifr Expression Detection, supplied by OriGene, 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/product/lifr/LIFR+Rabbit+Polyclonal+Antibody/pmc12915430-72-33-30
    Average 94 stars, based on 1 article reviews
    lifr expression detection - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    94
    OriGene lifr
    Expression validation of <t>LIFR</t> in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing <t>LIFR</t> <t>expression</t> patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.
    Lifr, supplied by OriGene, 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/product/lifr/LIFR+(NM_001127671)+Human+Untagged+Clone/pmc12915430-72-29-30
    Average 94 stars, based on 1 article reviews
    lifr - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    90
    Sino Biological lif receptor
    Expression validation of <t>LIFR</t> in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing <t>LIFR</t> <t>expression</t> patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.
    Lif Receptor, supplied by Sino Biological, 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/lifr/LIFR+Antibody%2C+Rabbit+PAb%2C+Antigen+Affinity+Purified/pm41543620-74-210-217
    Average 90 stars, based on 1 article reviews
    lif receptor - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    92
    Proteintech anti lifr
    Expression validation of <t>LIFR</t> in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing <t>LIFR</t> <t>expression</t> patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.
    Anti Lifr, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lifr/LIFR+Antibody/pm41380876-151-18-21
    Average 92 stars, based on 1 article reviews
    anti lifr - by Bioz Stars, 2026-09
    92/100 stars
      Buy from Supplier

    Image Search Results


    (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of lifr expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.

    Journal: bioRxiv

    Article Title: The LIF-LIFR Axis Promotes Liver Regeneration via Modulation of Angiogenesis and HGF Release from LSECs

    doi: 10.64898/2026.02.24.707802

    Figure Lengend Snippet: (A) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy (HEA1+HEA2) mice. The top panel is a bar plot of lifr expression, the bottom panel is a bubble plot of multiple receptors as indicated. (B) Expression of IL-6 family receptors in scRNA-seq across cell types of livers from healthy human. The top panel is a bar plot of LIFR expression, the bottom panel is a bubble plot of multiple receptors as indicated. (C) Circular network plot of LIF-LIFR interaction between different cell types in liver from healthy human (HEA5). (D) qPCR of lifr in isolated LSECs and whole liver from lifr f/f and lifrΔEC mice. (E) Western blot of LIFR in isolated LSECs from lifr f/f and lifrΔEC mice. (F) Liver-to-body weight ratio at 24 h post-PHx in male lifr f/f and lifrΔEC mice. (G) Liver-to-body weight ratio at 24 h post-PHx in female lifr f/f and lifrΔEC mice.

    Article Snippet: TaqMAn® expression assays were used: Actb (Mm02619580_g1), Anpep (Mm00476227_m1), Cdh5 (Mm00486938_m1), Hgf (Mm01135184_m1), Kdr (Mm01222421_m1), Lifr (Mm00442942_m1), Lyve1 (Mm00475056_m1), Pdgfrb , (Mm00435546_m1), Pecam (Mm01242576_m1).

    Techniques: Expressing, Isolation, Western Blot

    (A-C) Proliferation assays of primary LSECs treated with increasing doses of hLIF (A), hOSM (B) or hCT-1 (C). 100 ng/mL hLIF was used as positive control. (D) Proliferation assays of LSECs isolated from lifrΔEC mice treated with increasing doses of hLIF. (E&F) Proliferation assays of LSECs isolated from lifr f/f (E) or lifrΔEC (F) mice treated with increasing doses of hVEGF. (G&H) Western blot analysis of primary LSECs treated with hVEGF (G) or hLIF (H) (I) Western blot of primary hepatocytes treated with hLIF. (J) Proliferation assays of primary hepatocytes treated with increasing doses of hLIF. (K) Proliferation assays of AML12 cells treated with increasing doses of hLIF. (L) Immunofluorescence staining of AML12 cells treated with 80 ng/mL hHGF or hLIF. DAPI (blue), Ki67 (green). Scale bar: 50 μm.

    Journal: bioRxiv

    Article Title: The LIF-LIFR Axis Promotes Liver Regeneration via Modulation of Angiogenesis and HGF Release from LSECs

    doi: 10.64898/2026.02.24.707802

    Figure Lengend Snippet: (A-C) Proliferation assays of primary LSECs treated with increasing doses of hLIF (A), hOSM (B) or hCT-1 (C). 100 ng/mL hLIF was used as positive control. (D) Proliferation assays of LSECs isolated from lifrΔEC mice treated with increasing doses of hLIF. (E&F) Proliferation assays of LSECs isolated from lifr f/f (E) or lifrΔEC (F) mice treated with increasing doses of hVEGF. (G&H) Western blot analysis of primary LSECs treated with hVEGF (G) or hLIF (H) (I) Western blot of primary hepatocytes treated with hLIF. (J) Proliferation assays of primary hepatocytes treated with increasing doses of hLIF. (K) Proliferation assays of AML12 cells treated with increasing doses of hLIF. (L) Immunofluorescence staining of AML12 cells treated with 80 ng/mL hHGF or hLIF. DAPI (blue), Ki67 (green). Scale bar: 50 μm.

    Article Snippet: TaqMAn® expression assays were used: Actb (Mm02619580_g1), Anpep (Mm00476227_m1), Cdh5 (Mm00486938_m1), Hgf (Mm01135184_m1), Kdr (Mm01222421_m1), Lifr (Mm00442942_m1), Lyve1 (Mm00475056_m1), Pdgfrb , (Mm00435546_m1), Pecam (Mm01242576_m1).

    Techniques: Positive Control, Isolation, Western Blot, Immunofluorescence, Staining

    (A) Volcano plot of differentially secreted proteins from primary LSECs treated with 40 ng/mL LIF versus control (n = 4). (B&C) qPCR of lifr (B) and hgf (C) levels in LSECs isolated from lifr f/f mice with indicated treatments. (D) HGF concentrations in conditioned medium from LSECs treated with hLIF at the indicated doses. (E) HGF concentrations in conditioned medium from LSECs treated with 40 ng/mL hLIF in the presence of the STAT3 inhibitor C188-9 at the indicated doses. (F) HGF concentrations in conditioned medium from LSECs isolated from lifr f/f or lifrΔEC mice treated with hLIF, hCT-1 or hOSM. (G) Western blot analysis of hepatocytes co-cultured with LSECs with or without 40 ng/mL LIF. Quantification is shown in Figure S4C. (H) Model depicting LIF action on LSECs to stimulate angiogenesis and HGF release, thereby supporting hepatocyte proliferation via paracrine regulation.

    Journal: bioRxiv

    Article Title: The LIF-LIFR Axis Promotes Liver Regeneration via Modulation of Angiogenesis and HGF Release from LSECs

    doi: 10.64898/2026.02.24.707802

    Figure Lengend Snippet: (A) Volcano plot of differentially secreted proteins from primary LSECs treated with 40 ng/mL LIF versus control (n = 4). (B&C) qPCR of lifr (B) and hgf (C) levels in LSECs isolated from lifr f/f mice with indicated treatments. (D) HGF concentrations in conditioned medium from LSECs treated with hLIF at the indicated doses. (E) HGF concentrations in conditioned medium from LSECs treated with 40 ng/mL hLIF in the presence of the STAT3 inhibitor C188-9 at the indicated doses. (F) HGF concentrations in conditioned medium from LSECs isolated from lifr f/f or lifrΔEC mice treated with hLIF, hCT-1 or hOSM. (G) Western blot analysis of hepatocytes co-cultured with LSECs with or without 40 ng/mL LIF. Quantification is shown in Figure S4C. (H) Model depicting LIF action on LSECs to stimulate angiogenesis and HGF release, thereby supporting hepatocyte proliferation via paracrine regulation.

    Article Snippet: TaqMAn® expression assays were used: Actb (Mm02619580_g1), Anpep (Mm00476227_m1), Cdh5 (Mm00486938_m1), Hgf (Mm01135184_m1), Kdr (Mm01222421_m1), Lifr (Mm00442942_m1), Lyve1 (Mm00475056_m1), Pdgfrb , (Mm00435546_m1), Pecam (Mm01242576_m1).

    Techniques: Control, Isolation, Western Blot, Cell Culture

    Expression validation of LIFR in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing LIFR expression patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.

    Journal: Journal of Inflammation Research

    Article Title: Association of Increased Nasal Fluids-Serum Concordance of Protein Profile with Prognosis in Nasal Polyps

    doi: 10.2147/JIR.S567454

    Figure Lengend Snippet: Expression validation of LIFR in CRSwNP. ( A ) Transcriptional levels of biomarkers (LIFR, LIF, IL-5, IL-13) in PR versus non-PR groups. ELISA quantification of LIFR concentrations in both ( B ) serum and ( C ) NF of PR patients compared to non-PR and control groups. ( D ) Representative images of H&E and LIFR immunohistochemical staining (Magnification ×400). ( E ) Quantification of LIFR protein expression intensity (n=6/group). ( F and G ) scRNA-seq analysis of CRSwNP tissues showing LIFR expression patterns across cell populations (left: cell type clusters; right: LIFR expression). ( H ) Immunofluorescence of LIFR (red) co-localization with vascular endothelial cells (CD31+, green) and nuclear staining (DAPI, blue) at ×400 magnifications (n=6/group). * P < 0.05, ** P < 0.01, **** P < 0.0001.

    Article Snippet: After 1 h blocking with 10% BSA at room temperature, sections were incubated overnight at 4°C with primary antibodies, including neutrophil elastase (NE; Abcam #ab68672) for neutrophil quantification or LIFR (Origene #TA386958) for LIFR expression detection, followed by DAB substrate.

    Techniques: Expressing, Biomarker Discovery, Enzyme-linked Immunosorbent Assay, Control, Immunohistochemical staining, Staining, Immunofluorescence