Western blot analysis of extracts from HUVEC cells treated with serum using PPAR-BP (Phospho-Thr1457) Antibody. The lane on the left is treated with the antigen-specific peptide.
Rabbit Polyclonal antibody to MED1 (phospho Thr1457)The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. It also regulates p53-dependent apoptosis and it is essential for adipogenesis. This protein is known to have the ability to self-oligomerize. [provided by RefSeq, Jul 2008]
Immunogen
Peptide sequence around phosphorylation site of Threonine 1457 (A-Y-T(p)-P-Q) derived from Human PPAR-BP.
Modification
p-Thr1457
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WB
WB: 1:500 - 1:1000:
Species Reactivity
HumanMouse
Concentration
1mg/ml (Please refer to the vial label for the specific concentration)
The antibody detects endogenous level of PPAR-BP only when phosphorylated at Threonine 1457.
Application
Application
Western blot analysis of extracts from HUVEC cells treated with serum using PPAR-BP (Phospho-Thr1457) Antibody. The lane on the left is treated with the antigen-specific peptide.
Application Notes
WB: 1:500 - 1:1000:
Additional Information
Form
Liquid
Storage Instructions
Store at -20˚C/1 year
Storage Buffer
Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.