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Обратной транскриптазы структурированное изображение

Обратной транскриптазы

  • английское имяREVERSE TRANSCRIPTASE
  • CAS №9068-38-6
  • CBNumberCB4702207
  • мольный вес0
  • EINECS232-964-5
  • номер MDLMFCD00283754
  • файл MolMol file
химическое свойство
температура хранения -20°C
форма Liquid
цвет colorless
Биологические источники Porcine intestinal mucosa
Конкретная деятельность ≥10,000units/mL
≥5,000units/mg protein
UNSPSC Code 41105600
NACRES NA.55
Заявления об опасности и безопасности
WGK Германия 3
кода HS 3504009000

Обратной транскриптазы химические свойства, назначение, производство

Описание

Enzyme possessed by retroviruses that allows transcription of DNA from an RNA template. Such an enzyme has never been isolated from other sources, but speculation about its possible occurrence continues. Such an enzyme is widely used experimentally in genetic engineering to allow the formation of complementary DNA (cDNA) from purified RNA. The discovery of this enzyme faulted the widely held central dogma, which stated that the information flow in nature was always from DNA to RNA.

Использование

Synthesizes a complementary DNA strand using single-stranded RNA or DNA in the presence of a primer

Общее описание

M-MLV (Moloney murine leukemia virus) reverse transcriptase enzyme is isolated from E. coli expressing a portion of the pol gene of M-MLV on a plasmid. MoMLV RT is made up of 671 amino acid residues. It is a DNA polymerase that uses single-stranded RNA, DNA, or an RNA-DNA hybrid (using a primer) to synthesize a complementary DNA strand.

Методы очистки

This enzyme produces the complementary DNA from the RNA (as template). These are purified by solubilising the virus with non-ionic detergents. Lysed virions are adsorbed on DEAE-cellulose or DEAE-Sephadex columns, and the enzymes are eluted with a salt gradient, then chromatographed on a phosphocellulose column and fractions with enzyme activity are eluted in a salt gradient. They are also purified from other viral proteins by affinity chromatography on a pyran-Sepharose column. [Verna Biochim Biophys Acta 473 1 1977, Smith Methods Enzymol 65 560 1980; see commercial catalogues for other transcriptases.]

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