Purified anti-RNA Polymerase II Antibody anti-RNA Polymerase II - CTD4H8,BioLegend,904001

This antibody is effective in immunoblotting, immunoprecipitation and ELISA. It can also be used in chromatin immunoprecipitation assays.The antibody CTD4H8 recognizes the C-terminal repeat of the largest subunit of RNA polymerase II from HeLa andS. cerevisiaecells. This antibody recognizes both the phosphorylated and unphosphorylated forms of the RNA polymerase II.Based on sequence identity, this clone is liable to react with a broad range of species.Clone CTD4H8 is also known as 4H8 or CTD 4H8.Predicted MW is ~ 217 kD, Observed MW is on WB gel is ~240 kD

Host

Mouse

Reactivity

Human, Mouse, Rat

Application

WB -Quality testedICC -Verified

Platform ID

BAB716557940

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Product Specifications
Scientific Background

Specifications

NamePurified anti-RNA Polymerase II Antibody anti-RNA Polymerase II - CTD4H8
Cat. No.904001
HostMouse
RRIDAB_2565036 (BioLegend Cat. No. 904001)
IsotypeMouse IgG1, κ
ReactivityHuman, Mouse, Rat
ApplicationWB -Quality testedICC -Verified
ClonalityMonoclonal
Clone NumberCTD4H8
Concentration1 mg/ml
TargetRNA Polymerase II
ImmunogenThe immunogen used was a peptide containing 10 repeats of the synthetic peptide YSPTSPS using chemically synthesized phospho-ser5.
PurityThe antibody was purified by affinity chromatography.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
StorageThe antibody solution should be stored undiluted between 2°C and 8°C. Please note the storage condition for this antibody has been changed from -20°C to between 2°C and 8°C. You can also check your vial or your CoA to find the most accurate storage condition for this antibody.
Regulatory StatusResearch Use Only

Scientific Background

RPB1 is the catalytic and largest component of RNA polymerase II, which synthesizes mRNA precursors and many functional non-coding RNAs. It forms the polymerase active center together with RPB2, the second largest subunit. Polymerase II (Pol II) is the central component of the basal RNA polymerase II transcription machinery. It is composed of mobile elements that move relatively to each other. RPB1 is part of the core element with the central large cleft, the clamp element that moves to open and close the cleft, and the jaws that are thought to grab the incoming DNA template. At the start of transcription, a single DNA template strand of the promoter is positioned within the central active site cleft of Pol II. Then, a bridging helix emanates from RPB1 and crosses the cleft near the catalytic site, which acts as a ratchet that moves the RNA-DNA hybrid through the active site by switching from straight to bent conformations during each neuocleotide addition. This promotes translocation of Pol II. Pol II moves on the template during transcription elongation. Elongation is influenced by the phosphorylation status of the C-terminal domain (CTD) of Pol II's largest subunit (RPB1), which serves as a platform for assembling factors that regulate transcription initiation, elongation, termination, and mRNA processing. It can act as a RNA-dependent RNA polymerase when associated with small delta antigen of Hepatitis delta virus, being able to conform as both a replicate and transcriptase for the viral RNA circular genome.

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