Sequencing of coding parts of the human genome

Determining the level of biochemical parameters

Determining the level of urine indicators

Material sustainability study

Biodegradation Profile Study

Study of the effectiveness of the sterilization regime

Identification of causative agents of nosocomial infections

Protein engineering

Tests of combinations of enzyme preparations and modifiers

Lifetime new biological substances

Preparative Preparation of Characterized Monoclonal…

Technical testing of medical device (MI) (1 item)

Development and manufacture of experimental samples

Isolation and characterization of new antimicrobial…

Testing the metabolic and chemical stability of the…

Test metabolism compounds in the panel in vitro ADME…

Test metabolism compounds on the express panel ADME…

Tests to assess the risk of interactions interactions…

Testing the toxicity of compounds on the panel in vitro…

Research trials on the prediction of possible metabolites

Pilot pharmacokinetics test with determination of basic…

Laboratory of bioanalytics

Works and services for the creation of prototypes of…

Preparation and support of the registration process

Development and implementation of a management system

Analysis of the expression of polyA transcripts

Analysis of miRNA expression, 1 sample, at least 5…

Obtaining polyA fraction of RNA from a customer’s biological…

Library sequencing

Analysis of gene expression in FFPE samples

Isolation of nucleic acid fraction

NGS-based genome sequencing

Development of individual test systems

Genome-wide amplification

Research on the search for mutations and their verification…

Analysis of single cells and the study of their specific…

Sequencing

Preparation of genomic DNA shotgun libraries (1-12…

Preparation of RNA libraries (1-12 samples)

Preparation of libraries with a long insert (3-10 Kb,…

Preparation of amplicon libraries (1-24 samples)

Preparation of exomic libraries (1-12 samples)

Cultivation

Obtaining experimental batches of dry biomass

Development of experimental batches of finished forms

Preparation of a clinical study protocol

Development of a monitoring plan

Writing informed consent

Medical and scientific expertise of the project

Development of basic principles and protocol synopsis

Check and amendment of the protocol