Description
Instant freeze (FF)Freezing in histological gel O.C.T.
Fixing in the RNA stabilizer
Formalin fixation, automated histological wiring and paraffin block preparation (FFPE)
Production of slices from paraffin blocks and preparation of histopreparations
Preparation of matrix O.C.T. TMA block of frozen samples
Preparation of matrix paraffin TMA block from FFPE samples on the basis of molds on 2 mm / 60 holes, etc.
Automated preparation of matrix paraffin TMA block from FFPE samples with a sample size of 0.6, 1, 1.5 or 2 mm
Production of slices from paraffin TMA blocks and preparation of TMA histopreparations
Production of harmonized TMA histopreparations of normal tissues for the study of cross-reactivity of biosimilars
Lyse tissue
Preservation of viable tissue fragments using cryobiology protocols
Dissociation of tissues, isolation and preservation of viable cells using cryobiology protocols
Isolation of lymph nodes and preservation of viable mononuclear cells (monocytes and lymphocytes)
Isolation from tumors and preservation of viable tumor-infiltrating lymphocytes (TIL)
The establishment of primary cell cultures and the expansion of cells in vitro, the preservation of viable cells using cryobiology protocols
Isolation of serum
Isolation of blood plasma (EDTA, Li-Hep, Na-Hep) by the standard method
Double and triple unscrew plasma isolation (citrate, BCT, etc.)
Instant saliva freeze
DNA stabilization of saliva
Instant freezing of urine
Isolation of urine fractions (with lysing and instant freezing of cell urine sediment, preservation of cell fraction using cryobiology protocols, freezing of the supernatant)
Freezing of whole blood samples for DNA extraction
Preparation of blood smears
Stabilization of blood nucleic acids (DNA and RNA using PAXgene systems)
Isolation of viable peripheral blood mononuclear cells (PBMCs), their preservation using cryobiology protocols
Isolation of viable peripheral blood mononuclear cells (PBMCs), their instant freezing (FF)
Preparation of blood prints on filters
Instant freezing of bone marrow aspirate samples
Preparation of bone marrow aspirate smears
Stabilization of bone marrow RNA (using PAXgene systems)
Isolation of viable mononuclear cells of the bone marrow (IADC), their preservation using cryobiology protocols
Isolation of viable mononuclear cells of the bone marrow (IADM), their instant freezing (FF)
Preparation of instantly frozen samples of bone marrow aspirate clots
Preparation of paraffin blocks (FFPE) from samples of bone marrow aspirate by pouring in OCT-gel or from clots.
Isolation of various biological fluid fractions (exudate, wound discharge, ascites fluid, synovial fluid, etc.) (with lizirovanie and instant freezing of cell urine sediment, preservation of cell fraction using cryobiology protocols, supernatant freezing)
Magnetic sorting of viable cells (MACS) by surface markers (CD34 +, CD133 +, CD138 +, etc.), instant freezing of cell fractions or their preservation using cryobiology protocols
Isolation of RNA from stabilized and instantly frozen tissue samples, and measurement of the RIN index (RNA integrity index)
Isolation of RNA from stabilized blood samples and measurement of the RIN index
Isolation of RNA from stabilized and instantly frozen bone marrow aspirate samples, and measurement of the RIN index
DNA isolation from different types of tissue samples
DNA isolation from blood samples
DNA isolation from bone marrow aspirate samples
Determination of nucleic acid concentration
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