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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Transcription >> Polymerase associated factors >> Pol II Transcription >> Other
Anti-TRAP220/MED1 antibody
See all TRAP220/MED1 products (8) ...
Rabbit polyclonal to TRAP220/MED1
ELISA, IHC-P, WBmore details
Reacts with
Mouse, Human
Synthetic peptide derived from internal region of human TRAP220/MED1
Human breast carcinoma tissue. Extracts from Jurkat cells.
Liquid
Store at -20°C. Stable for 12 months at -20°C
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS, 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Epigenetics and Nuclear Signaling >> Nuclear Signaling Pathways >> Nuclear Receptors >> Co-activators/co-repressors
Epigenetics and Nuclear Signaling >> Transcription >> Polymerase associated factors >> Pol II Transcription >> Other
Our Abpromise guarantee covers the use of ab64965 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: 1/10000
IHC-P: 1/50 - 1/100.Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
WB: 1/500 - 1/1000.Detects a band of approximately 170 kDa (predicted molecular weight: 180 kDa).
Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors.
Ubiquitously expressed.
Belongs to the Mediator complex subunit 1 family.
Phosphorylated by MAPK1 or MAPK3 during G2/M phase which may enhance protein stability and promote entry into the nucleolus. Phosphorylated upon DNA damage, probably by ATM or ATR.
Nucleus. A subset of the protein may enter the nucleolus subsequent to phosphorylation by MAPK1 or MAPK3.
Target information above from: UniProt accessionQ15648
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - TRAP220/MED1 antibody (ab64965)

All lanes : Anti-TRAP220/MED1 antibody (ab64965) at 1/500 dilution
Lane 1 : extracts from Jurkat cells, without immunising peptide
Lane 2 : extracts from Jurkat cells, with immunising peptide
Predicted band size : 180 kDa
Observed band size : 170 kDa (why is the actual band size different from the predicted?)
Additional bands at : 110 kDa. We are unsure as to the identity of these extra bands.
The amount of positive control loading for the WB is 5-30 ug of total protein. The amount of the peptide for the WB is 5-10 ug.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - TRAP220/MED1 antibody (ab64965)

Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue using 1/50 ab64965, after antigen retrieval by boiling in a pressure cooker for 2-3 min. Polymer system was used for signal enhancing and DAB staining was performed for visualising the signal.
This product has been referenced in:
See all 2 publications for this product
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All lanes : Anti-TRAP220/MED1 antibody (ab64965) at 1/500 dilution
Lane 1 : extracts from Jurkat cells, without immunising peptide
Lane 2 : extracts from Jurkat cells, with immunising peptide
Predicted band size : 180 kDa
Observed band size : 170 kDa (why is the actual band size different from the predicted?)
Additional bands at : 110 kDa. We are unsure as to the identity of these extra bands.
The amount of positive control loading for the WB is 5-30 ug of total protein. The amount of the peptide for the WB is 5-10 ug.

Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue using 1/50 ab64965, after antigen retrieval by boiling in a pressure cooker for 2-3 min. Polymer system was used for signal enhancing and DAB staining was performed for visualising the signal.
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