Anti-HEY1 antibody
4
(2 Reviews)
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(23 Publications)
Rabbit Polyclonal HEY1 antibody. Suitable for WB, ICC/IF and reacts with Human samples. Cited in 23 publications. Immunogen corresponding to Recombinant Fragment Protein within Human HEY1 aa 1 to C-terminus.
View Alternative Names
BHLHB31, CHF2, HERP2, HESR1, HRT1, HEY1, Hairy/enhancer-of-split related with YRPW motif protein 1, Cardiovascular helix-loop-helix factor 2, Class B basic helix-loop-helix protein 31, HES-related repressor protein 1, Hairy and enhancer of split-related protein 1, Hairy-related transcription factor 1, CHF-2, bHLHb31, HESR-1, HRT-1, hHRT1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-HEY1 antibody (AB154077)
ab154077 staining HEY1 in HeLa cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 4% paraformaldehyde. Samples were incubated with primary antibody (1/2000) (green). Alpha tubulin stained red and nuclei stained blue
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-HEY1 antibody (AB154077)
ab154077 staining HEY1 in H1299 cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 4% paraformaldehyde. Samples were incubated with primary antibody (1/1000) (green). Nuclei were stained blue with Hoechst 33342
- WB
Unknown
Western blot - Anti-HEY1 antibody (AB154077)
12% SDS PAGE
All lanes:
Western blot - Anti-HEY1 antibody (ab154077) at 1/1000 dilution
Lane 1:
A549 whole cell lysate at 30 µg
Lane 2:
H1299 whole cell lysate at 30 µg
Lane 3:
HCT116 whole cell lysate at 30 µg
Lane 4:
MCF-7 whole cell lysate at 30 µg
Predicted band size: 33 kDa
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- WB
CiteAb
Western blot - Anti-HEY1 antibody (AB154077)
HEY1 western blot using anti-HEY1 antibody ab154077. Publication image and figure legend from Jiang, S., Zhou, F., et al., 2020, J Cancer, PubMed 32284759.
ab154077 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab154077 please see the product overview.
HEY1 is a key factor in the tumorigenicity of 143B osteosarcoma cells. (A) Protein expression level of HEY1 in six osteosarcoma cell lines (MG-63, Saos-2, U-2 OS, MNNG/HOS, 143B, and SJSA-1). (B) Protein expression level of HEY1 after lentivirus-mediated RNA interference in 143B osteosarcoma cells. (C) Lentivirus infection efficiency detected by fluorescence microscopy (scale bar = 200 μm). (D) Lentivirus-infected 143B osteosarcoma cell pellet under visible light. (E) Images of 143B cell-bearing mice under 530-nm laser irradiation at the experimental endpoint. Subcutaneous tumors at the experimental endpoint (F), tumor growth curves (G), and tumor weight (H) are shown. (I) Protein expression level of HEY1 in Saos-2 and HEY1-overexpressed Saos-2 cells. (J) Tumorigenicity assay of Saos-2 cells after HEY1-overexpression. Subcutaneous tumors at the experimental endpoint (K), tumor growth curves (L), and tumor weight (M) of Saos-2 cells after HEY1-overexpression are shown.
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Reactivity data
Properties and storage information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
HEY1 functions as an important regulator of developmental processes. It participates in the Notch signaling pathway and regulates the transcription of genes involved in cell fate decisions. HEY1 forms a part of transcriptional complexes often associating with other proteins to modulate expression patterns important for differentiation and proliferation. These complexes enable it to exert control over target gene expression influencing processes like angiogenesis and myogenesis.
Pathways
HEY1 is prominently involved in the Notch signaling and Wnt pathways. Notch signaling regulates cell communication important for cell differentiation while the Wnt pathway influences cell growth and development. In both pathways HEY1 modulates signal transduction by interacting with proteins like RBPJ in the Notch pathway. HEY1's role in these pathways reveals its importance in maintaining cellular architecture and instructive developmental cues.
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Publications (23)
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Acta neuropathologica communications 11:198 PubMed38102708
2023
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Molecular carcinogenesis 63:22-33 PubMed37877736
2023
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Cells 11: PubMed36231088
2022
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Cell stem cell 29:1402-1419.e8 PubMed36055194
2022
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Thoracic cancer 13:1961-1973 PubMed35599381
2022
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Nature communications 13:1537 PubMed35318302
2022
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Journal of materials science. Materials in medicine 33:4 PubMed34940936
2021
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Bioengineered 12:10878-10890 PubMed34666595
2021
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Molecular medicine (Cambridge, Mass.) 27:103 PubMed34496740
2021
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European journal of pharmacology 906:174268 PubMed34166702
2021
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