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R0884

Sigma-Aldrich

RNA-Polymerase, T7 aus E. coli HMS 174/pAR1219

recombinant, expressed in E. coli, buffered aqueous solution

Synonym(e):

T7-RNA-Polymerase

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About This Item

CAS-Nummer:
EC-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352204

Rekombinant

expressed in E. coli

Qualität

for molecular biology

Form

buffered aqueous solution

Mol-Gew.

98.8 kDa

Konzentration

10,000-50,000 U/mL

UniProt-Hinterlegungsnummer

Fremdaktivität

DNase and RNase, none detected

Lagertemp.

−20°C

Angaben zum Gen

bacteriophage T7 ... T7p07(1261050)

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Allgemeine Beschreibung

T7 RNA polymerase is highly specific for the bacteriophage T7 promoter and terminator sequences. It is extensively used to prepare RNA transcripts for stuctural and metabolic studies. The RNA transcripts can be converted to probes for sensitive hybridization detection studies. T7 polymerase and dideoxynucleotides can be used to directly sequence DNA.

Komponenten

T7 RNA Polymerase is supplied as a solution of 100 mM NaCl, 50 mM Tris-HCl (pH 7.9), 0.1 mM EDTA, 0.1% Triton X-100, 1 mM DTT, and 50% (v/v) glycerol.

Einheitendefinition

One unit will catalyze the incorporation of 1 nmol of rNTP into acid-precipitable material in 60 min at 37°C.

Hinweis zur Analyse

Activity assay: 40 mM Tris-HCl, pH 7.9, 6 mM MgCl2, 4 mM spermidine, 10 mM DTT, 0.5 μM each rNTP + 10 μCi α-32P-UTP, 3-10 units of enzyme, and 1 μg of a 350 bp template are incubated for 10 min at 37°C in a total volume of 100 μl. Typical results are ≥50% incorporation of labeled nucleotide into ≥90% full-length transcript.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Kunden haben sich ebenfalls angesehen

Characterization of T7-specific ribonucleic acid polymerase. 1. General properties of the enzymatic reaction and the template specificity of the enzyme.
M Chamberlin et al.
The Journal of biological chemistry, 248(6), 2235-2244 (1973-03-25)
Byung-Chun Kim et al.
Journal of microbiology and biotechnology, 23(2), 189-194 (2013-02-16)
In a study of hydrogen-producing bacteria, strain T4384 was isolated from rice field samples in the Republic of Korea. The isolate was identified as Enterobacter sp. T4384 by phylogenetic analysis of 16S rRNA and rpoB gene sequences. Enterobacter sp. T4384
Ran Furman et al.
FEBS letters, 587(6), 614-619 (2013-02-19)
Transcription factor DksA contains a four-Cys Zn(2 +)-finger motif thought to be responsible for structural integrity and the relative disposition of its domains. Pseudomonas aeruginosa encodes an additional DksA paralog (DksA2) that is expressed selectively under Zn(2+) limitation. Although DksA2
Looking for a promoter in 3D.
Vladimir Svetlov et al.
Nature structural & molecular biology, 20(2), 141-142 (2013-02-06)
Yuko Murayama et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 69(Pt 2), 174-177 (2013-02-07)
DNA-dependent RNA polymerase (RNAP) synthesizes RNA complementary to the template DNA. During transcript elongation, RNAP often undergoes backward translocation ('backtracking') by dissociating the 3' end of the nascent RNA transcript from the template DNA. While the backtracked state of RNAP

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