Genome - Wide Methylated DNA
Immunoprecipitation Analysis of Patients with Polycystic Ovary Syndrome Hao - ran Shen, 1 Li - hua Qiu, 1 Zhi - qing Zhang, 2 Yuan - yuan Qin, 1 Cong Cao, 2, * andWen Di1, *
For Western blot assay and
immunoprecipitation analysis, CD4 + T cells were isolated from mice spleen on day 21 after transplantation using a Mouse CD4 + T Cell Isolation Kit (Miltenyi Biotec), and the procedures were performed as described previously (35).
(G)
Immunoprecipitation analysis of the acetylation of Akt.
Previous whole - genome chromatin
immunoprecipitation analyses have identified a wide set of Oct4 target genes [6], [28], as well as describing co-occupancy of Oct4 and other transcription factors at many of these genes [6].
Not exact matches
Chromatin
immunoprecipitation sequencing
analysis revealed enrichment of H3K27me3 at specific loci in KDM6A - null cells, including PRC2 / EZH2 and their downstream targets.
Services include global and gene - specific DNA methylation
analysis, and chromatin
immunoprecipitation (ChIP) followed by library preparation in a high - throughput format (HT ChIP - Seq).
(e, g) Western blot (WB)
analysis of tyrosine phosphorylation (pTyr) and total Tie2 after Tie2
immunoprecipitation (IP) in BP (e) and HUVEC (g) upon stimulation with recombinant human (rh) Ang1 compared to unstimulated (us) cells.
Importantly, this is one of the first reports applying Aβ
immunoprecipitation followed by MALDI - MS
analysis in CSF from a transgenic AD model, providing a robust, novel platform for the assessment of Aβ expression profiles in biological fluids of transgenic models.
To evaluate whether loss of ABL kinases affected TAZ activity, we performed chromatin
immunoprecipitation (ChIP)
analysis using primers for TAZ targets identified by ChIP sequencing
analysis (42).
Chromatin
immunoprecipitation and chip
analyses revealed that both active and silenced genes in ES cells are directly bound by one or more of these three proteins [17], [19].
Here we present fCCAC, an application of functional canonical correlation
analysis to assess covariance of nucleic acid sequencing datasets such as chromatin
immunoprecipitation followed by deep sequencing (ChIP - seq).
(D) Treatment with 1 mM 8 - Br - cAMP for four hours enhances Oct4 binding to genomic loci as determined by chromatin
immunoprecipitation, followed by real - time PCR
analysis at Nanog and fgf12 sites.
A detailed description of the methods and
analyses of methylated DNA
immunoprecipitation (MeDIP) and microarrays hybridization used in this study were previously described [43] and can be found in File S1.