Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade,Abcam,AB26721
Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade (ab26721) is a rabbit polyclonal antibody and is validated for use in ChIP, ICC/IF, IHC-P, IP, WB in arabidopsis thaliana, caenorhabditis elegans, drosophila melanogaster, human, mouse, rat, saccharomyces cerevisiae, schizosaccharomyces pombe, xenopus laevis, zebrafish samples. Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade (ab26721) has been cited over 55 times in peer reviewed journals and is trusted by the scientific community. Abcam's high quality validation processes ensure Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade (ab26721) has high sensitivity and specificity. Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade (ab26721) has 8 independent reviews from customers. Anti-RNA polymerase II CTD repeat YSPTSPS antibody - ChIP Grade (ab26721) specifically detects RNA polymerase II CTD repeat YSPTSPS (UniProt ID: P24928; Molecular weight: 217kDa) and is sold in 100 µg selling sizes. RNA polymerase II CTD repeat YSPTSPS is essential for transcription regulation and gene expression. Utilizing our highly specific RNA polymerase II CTD repeat YSPTSPS antibody can significantly enhance the detection and study of this modification. Research indicates that phosphorylation of the CTD repeat YSPTSPS is crucial for the transition from transcription initiation to elongation, impacting various cellular processes and disease states. Phosphorylation of RNA polymerase II at the CTD repeat YSPTSPS is critical for proper mRNA synthesis and processing. Abnormal phosphorylation patterns are linked to transcriptional dysregulation in cancer, pediatric gliomas, chondroblastomas, and neurodevelopmental syndromes. Studying these modifications can provide insights into potential therapeutic targets for various conditions.
Host
Rabbit
Reactivity
Human
Application
IP, WB, ChIP, ICC/IF, IHC-P
Platform ID
BAB833011900

Abcam
Contact
Tel: +44 (0)1223 696000
Fax: +44 (0)1223 215 215
Email:
Specifications
Scientific Background
Target data Catalytic core component of RNA polymerase II (Pol II), a DNA-dependent RNA polymerase which synthesizes mRNA precursors and many functional non-coding RNAs using the four ribonucleoside triphosphates as substrates (By similarity) (PubMed : 23748380, PubMed : 27193682, PubMed : 30190596, PubMed : 9852112). Pol II-mediated transcription cycle proceeds through transcription initiation, transcription elongation and transcription termination stages. During transcription initiation, Pol II pre-initiation complex (PIC) is recruited to DNA promoters, with focused-type promoters containing either the initiator (Inr) element, or the TATA-box found in cell-type specific genes and dispersed-type promoters that often contain hypomethylated CpG islands usually found in housekeeping genes. Once the polymerase has escaped from the promoter it enters the elongation phase during which RNA is actively polymerized, based on complementarity with the template DNA strand. Transcription termination involves the release of the RNA transcript and polymerase from the DNA (By similarity) (PubMed : 23748380, PubMed : 27193682, PubMed : 28108474, PubMed : 30190596, PubMed : 9852112). Forms Pol II active center together with the second largest subunit POLR2B/RPB2. Appends one nucleotide at a time to the 3' end of the nascent RNA, with POLR2A/RPB1 most likely contributing a Mg(2+)-coordinating DxDGD motif, and POLR2B/RPB2 participating in the coordination of a second Mg(2+) ion and providing lysine residues believed to facilitate Watson-Crick base pairing between the incoming nucleotide and template base. Typically, Mg(2+) ions direct a 5' nucleoside triphosphate to form a phosphodiester bond with the 3' hydroxyl of the preceding nucleotide of the nascent RNA, with the elimination of pyrophosphate. The reversible pyrophosphorolysis can occur at high pyrophosphate concentrations (By similarity) (PubMed : 30190596, PubMed : 8381534, PubMed : 9852112). Can proofread the nascent RNA transcript by means of a 3' -> 5' exonuclease activity. If a ribonucleotide is mis-incorporated, backtracks along the template DNA and cleaves the phosphodiester bond releasing the mis-incorporated 5'-ribonucleotide (By similarity) (PubMed : 8381534). Through its unique C-terminal domain (CTD, 52 heptapeptide tandem repeats) serves as a platform for assembly of factors that regulate transcription initiation, elongation and termination. CTD phosphorylation on Ser-5 mediates Pol II promoter escape, whereas phosphorylation on Ser-2 is required for Pol II pause release during transcription elongation and further pre-mRNA processing. Additionally, the regulation of gene expression levels depends on the balance between methylation and acetylation levels of the CTD-lysines. Initiation or early elongation steps of transcription of growth-factor-induced immediate early genes are regulated by the acetylation status of the CTD. Methylation and dimethylation have a repressive effect on target genes expression. Cooperates with mRNA splicing machinery in co-transcriptional 5'-end capping and co-transcriptional splicing of pre-mRNA (By similarity) (PubMed : 24207025, PubMed : 26124092).. RNA-dependent RNA polymerase that catalyzes the extension of a non-coding RNA (ncRNA) at the 3'-end using the four ribonucleoside triphosphates as substrates. An internal ncRNA sequence near the 3'-end serves as a template in a single-round Pol II-mediated RNA polymerization reaction. May decrease the stability of ncRNAs that repress Pol II-mediated gene transcription.. (Microbial infection) Acts as an RNA-dependent RNA polymerase when associated with small delta antigen of Hepatitis delta virus, acting both as a replicase and transcriptase for the viral RNA circular genome. See full target information POLR2A
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