Anti-TRAP220/MED1 (phospho T1457) antibody
5
(2 Reviews)
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(15 Publications)
Rabbit Polyclonal TRAP220/MED1 phospho T1457 antibody. Suitable for ChIP, ELISA, WB, IHC-P, ICC/IF and reacts with Mouse, African green monkey, Human samples. Cited in 15 publications. Immunogen corresponding to Synthetic Peptide within Human MED1 phospho T1457.
View Alternative Names
ARC205, CRSP1, CRSP200, DRIP205, DRIP230, PBP, PPARBP, PPARGBP, RB18A, TRAP220, TRIP2, MED1, Mediator of RNA polymerase II transcription subunit 1, Activator-recruited cofactor 205 kDa component, Mediator complex subunit 1, Peroxisome proliferator-activated receptor-binding protein, Thyroid hormone receptor-associated protein complex 220 kDa component, Thyroid receptor-interacting protein 2, Vitamin D receptor-interacting protein complex component DRIP205, p53 regulatory protein RB18A, PPAR-binding protein, Trap220, TR-interacting protein 2, TRIP-2
- IHC-P
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAP220/MED1 (phospho T1457) antibody (AB60950)
ab60950 at 1/50 - 1/100 dilution staining TRAP220/MED1 in human heart by Immunohistochemistry, Paraffin embedded tissue, in the absence or presence of the immunising peptide
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-TRAP220/MED1 (phospho T1457) antibody (AB60950)
ab60950 at 1/500 - 1/1000 dilution staining TRAP220/MED1 in HeLa cells by Immunofluorescence.
- WB
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Western blot - Anti-TRAP220/MED1 (phospho T1457) antibody (AB60950)
All lanes:
Western blot - Anti-TRAP220/MED1 (phospho T1457) antibody (ab60950) at 1/500 dilution
Lane 1:
HuvEc cell extractstreated with Serum (20%, 30mins)
Lane 2:
HuvEc cell extractstreated with Serum (20%, 30mins) with immunising peptide
Predicted band size: 168 kDa
Observed band size: 170 kDa
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- WB
CiteAb
Western blot - Anti-TRAP220/MED1 (phospho T1457) antibody (AB60950)
TRAP220/MED1 (phospho T1457) western blot using anti-TRAP220/MED1 (phospho T1457) antibody ab60950. Publication image and figure legend from Zhao, W., Breese, E., et al., 2013, PLoS One, PubMed 23630580.
ab60950 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 ab60950 please see the product overview.
TNFα induced formation of SIMPL-MED1 complexes is p65 dependent.(A) HEK 293 cells or (B) wild-type MEFs or MEFs lacking p65 were transfected with SIMPL-FLAG or empty FLAG-vector, 72 h later cells were left untreated (-) or treated with rhTNFα (10 ng/ml) for 45 min. Upper panels : immunocomplexing assays were performed with antibody to MED1 (IP : MED1) and/or FLAG (IP : FLAG) and immunocomplexed materials were subjected to Western analysis with the antibody to the proteins indicated on the right hand side of the figure. Lower panels : Cell lysates (50 ug) used in immunocomplexing assays were subjected to Western analysis with antibodies to the indicated proteins. (C) HEK 293 cells were transfected with the indicated constructs, 72 h later cells were left untreated or treated with rhTNFα (10 ng/ml) for 45 min. Cell lysates were either analyzed directly (panel labeled input) or were subjected to immunocomplexing assays with Flag-antibody coupled sepharose beads, materials bound to the agaroase beads were eluted with Flag peptide and subjected to immunocomplexing assays with antibody to p65. Immunocomplexed materials were subjected to Western analysis with the antibodies to the proteins indicated on the right hand side of the figure. All assays were repeated at least three times.
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Reactivity data
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TRAP220/MED1 functions within the larger mediator complex a multi-protein coactivator essential for gene transcription by RNA polymerase II. It plays an important role in nuclear receptor signaling facilitating the transcriptional activation by various nuclear hormone receptors. MED1 interacts directly with these receptors through its various domains allowing the transcription of target genes responsive to hormonal signals.
Pathways
TRAP220/MED1 contributes significantly to transcriptional activation pathways involving nuclear receptors such as the PPAR (Peroxisome Proliferator-Activated Receptor) and thyroid hormone receptor pathways. It closely interacts with other proteins in these pathways including MED12 and MED14 which form integral parts of the mediator complex's function. Its involvement in these pathways highlights its critical role in lipid metabolism and energy homeostasis.
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Publications (15)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:7065 PubMed40764481
2025
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NPJ breast cancer 11:39 PubMed40287441
2025
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Journal of experimental & clinical cancer research : CR 43:69 PubMed38443991
2024
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British journal of cancer 128:2326-2337 PubMed37076563
2023
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Nucleic acids research 51:99-116 PubMed36535377
2022
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Journal of visualized experiments : JoVE : PubMed35225292
2022
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Nucleic acids research 48:7182-7196 PubMed32510157
2020
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eNeuro 4: PubMed28955722
2017
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Genes to cells : devoted to molecular & cellular m 22:265-276 PubMed28151579
2017
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Chemical research in toxicology 27:1496-503 PubMed25068892
2014
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WB
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