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http://acervodigital.unesp.br/handle/11449/65686
- Title:
- Preparation of N2, N2,7-trimethylguanosine affinity columns
- CSIC
- Universidade Estadual Paulista (UNESP)
- Hospitalet de Llobregat
- EMBL
- 0732-8311
- 2,2,7-trimethylguanosine (TMG) binding proteins from human cells were purified through TMG-affinity columns. TMG synthesis was improved and the TMG obtained was shown to be similar to the TMG in the 5' cap of the UsnRNAs. The eluates obtained with TMG-affinity chromatographies were very different from those isolated with m7G-affinity columns, thus suggesting that specific TMG- binding proteins were obtained. The fraction may be enriched with factors associated with import and/or hypermethylation of UsnRNPs.
- 1-Jan-1999
- Nucleosides and Nucleotides, v. 18, n. 1, p. 125-136, 1999.
- 125-136
- binding protein
- guanosine derivative
- small nuclear RNA
- antibody
- carrier protein
- drug derivative
- fungal protein
- guanosine
- hemocyanin
- keyhole limpet hemocyanin
- keyhole-limpet hemocyanin
- monoclonal antibody
- N(2),N(2),7 trimethylguanosine
- N(2),N(2),7-trimethylguanosine
- nuclear protein
- sepharose
- serum albumin
- affinity chromatography
- animal experiment
- extraction
- human
- mouse
- nonhuman
- nucleotide metabolism
- protein methylation
- protein purification
- spliceosome
- synthesis
- animal
- cell nucleus
- chemistry
- cytoplasm
- HeLa cell
- instrumentation
- isolation and purification
- methodology
- rabbit
- Saccharomyces cerevisiae
- Animals
- Antibodies
- Antibodies, Monoclonal
- Carrier Proteins
- Cell Nucleus
- Chromatography, Affinity
- Cytoplasm
- Fungal Proteins
- Guanosine
- Hela Cells
- Hemocyanin
- Humans
- Mice
- Nuclear Proteins
- Rabbits
- Sepharose
- Serum Albumin
- http://dx.doi.org/10.1080/07328319908045599
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/65686
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