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.
IgG
Rabbit
pH: 7
Preservative: 0.025% Proclin 300
Constituents: 79% PBS, 20% Glycerol (glycerin, glycerine)
Liquid
Polyclonal
WB | ICC/IF | |
---|---|---|
Human | Tested | Tested |
Mouse | Predicted | Predicted |
Cow | Predicted | Predicted |
Dog | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/3000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Cow, Dog | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Cow, Dog | Dilution info - | Notes - |
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Transcriptional repressor which binds preferentially to the canonical E box sequence 5'-CACGTG-3' (PubMed:11095750). Downstream effector of Notch signaling required for cardiovascular development. Specifically required for the Notch-induced endocardial epithelial to mesenchymal transition, which is itself criticial for cardiac valve and septum development. May be required in conjunction with HEY2 to specify arterial cell fate or identity. Promotes maintenance of neuronal precursor cells and glial versus neuronal fate specification. Represses transcription by the cardiac transcriptional activators GATA4 and GATA6 and by the neuronal bHLH factors ASCL1/MASH1 and NEUROD4/MATH3 (PubMed:15485867). Involved in the regulation of liver cancer cells self-renewal (PubMed:25985737).
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
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.
IgG
Rabbit
pH: 7
Preservative: 0.025% Proclin 300
Constituents: 79% PBS, 20% Glycerol (glycerin, glycerine)
Liquid
Polyclonal
Affinity purification Immunogen
Blue Ice
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
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This supplementary information is collated from multiple sources and compiled automatically.
The HEY1 protein also known as Hes-related family bHLH transcription factor with YRPW motif 1 plays a significant role as a transcriptional repressor. It weighs approximately 33 kilodaltons. HEY1 is part of the hairy and enhancer of split family of proteins. Expression of HEY1 occurs in various tissues including the heart brain and liver. Within cells HEY1 localizes to the nucleus where it modulates gene expression by binding to specific DNA sequences.
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.
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.
HEY1 is associated with various cancers and cardiovascular diseases. Abnormal HEY1 expression correlates with tumorigenesis in cancers such as osteosarcoma where it may interact with proteins like HES1 to influence tumor growth. Additionally HEY1's involvement in cardiovascular diseases links to its role in regulating vascular remodeling and heart development where an imbalance in HEY1 expression might contribute to pathological outcomes.
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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
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
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
Image collected and cropped by CiteAb under a CC-BY license from the publication
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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