+34 9340006100 -ext. 437807-info@nanbiosis.com

Posts on Jan 1970

U1.E05. Tangential filtration Unit for purification

Tangential filtration Unit for purification.

U1.E05_TANGENTIAL FILTRATION UNIT FOR PURIFICATION_1
Read More

U1.E04. FPLC ÄKTA Chromatography systems for purification

FPLC ÄKTA Chromatography systems for purification

ÄKTA Purifier equipment for protein purification
Read More

U1.E03. Incubator shaker with cooling unit for insect cells suspension cultures

Incubator shaker with cooling unit for insect cells suspension cultures.

U1.E03_INCUBATOR SHAKER WITH COOLING UNIT FOR INSECT CELL SUSPENSION
Read More

U1.E02. 10 liter WAVE bioreactor for insect cells

10 liter WAVE bioreactor for insect cells.

U1.E02_10 LITER WAVE BIOREACTOR FOR INSECT CELLS
Read More

U1.E01. 2 and 7 liter bioreactors for bio production

2 and 7 liter bioreactors for bio production

U1.E01_2 AND 7 LITER BIOREACTORS FOR BIO PRODUCTION_1
Read More

U1-S06. Criopreservation (On-site&Remote)

Criopreservation of Proteins, Plasmids, etc

Read More

U1-S04. Consultancy in protein production (On-site&Remote)

In all matters dealing with protein production, expresion systems, etc, according to the final application of the product.

Read More

U1-S03: Proteins purification (On-site&Remote) OUTSTANDING

  • Identification of the most appropriate strategy for purification, given the physical and chemical properties, opting either for purification modules or, in the case of fusion proteins, elements which enable purification by affinity.
  • Purification (downstream processing) using FPLC chromatography and/or tangential filtration.
  • Quality control of the purified protein ( molecular weight and purity by SDS-PAGE, biological activity, conformation by FTIR and DLS.
Read More

U1-S02. Bioproduction of proteins (On-site&Remote) OUTSTANDING

  • Production of the plasmid DNA that contains the gene of the relevant protein to be incorporated into the producing cells by transformation/transfection.
  • Selection of the optimal protein production conditions using small and medium-scale expression; confirmation of the expression using Westernblot and SDS-PAGE analysis and quantification by densitometry.
  • Measurements of the solubility/aggregation of the protein under study.
  • Scale-up of the upstream processing in bioreactors or incubator shaker according to requirements.”
Read More

U1-S01. Molecular cloning (On-site&Remote) OUTSTANDING

  • Identification of the most appropriate system, selecting between Escherichia coli, insect cells (with expression systems based on infection with Baculovirus) and mammalian cells, according to the characteristics of the desired protein in terms of its size, modifications, etc.
  • Cloning of the gene that codifies for the protein of interest in the chosen expression vector; selection of the positive genes and their characterization by sequencing.
Read More