What are HeLa and HEp 2 cells
Translation of "HEp- 2" in German
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HEp- 2 cells are recommended for isolation.
Be for isolation HEp- 2 Cells recommended.
HEp- 2 cells are the most widely used for growth.
For growth are usually HEp- 2 Cells used.
Continuous human epithelial cell lines such as HeLa or HEp- 2 appear to be the most sensitive cell lines for primary isolation of RSV.
Continuous human epithelial cell lines, e.g. B: HeLa or HEp- 2 , appear to be the most sensitive cell lines for primary isolation from RSV.
Cell culture isolation of RSV can be attained with a number of cell lines including HEp- 2, HeLa, A 549, and Vero cells.
Cell culture isolation of RSV can be done using one or more cell lines, including HEp- 2 , HeLa, A 549 and Vero cells.
Each control slide contains one positive and one negative well with infected (RSV, Long Strain) and uninfected HEp- 2 cells, respectively, fixed with acetone.
Each control slide contains a positive well with infected (RSV, strain Long) HEp-2 cells and a negative well with uninfected cells HEp- 2 -Cells fixed with acetone.
Primary monkey kidney cells, MDCK, LLC-MK 2, HEp- 2, or other cells known to be susceptible to the different respiratory viruses are recommended for isolation.
Primary monkey kidney cells, MDCK, LLC-MK 2, HEp- 2 or other cells susceptible to the various respiratory viruses are recommended.
METHODS FOR ACQUIRING SHAPES FROM HEP-2 CELL SECTIONS AND THE CASE-BASED RECOGNITION OF HEP-2 CELLS
The method of claim 5, wherein said cells are HEp-2, macrophages, macrophage cell lines or McCoy cells.
The method of claim 5 wherein the cells HEp-2, Macrophages, macrophage cell lines, or McCoy cells.
BIOCHIP combination of HEp-2 cells and prime liver for ANA diagnostics
BIOCHIP combination of HEp-2 cells and primate liver for ANA diagnostics
high throughput HEp-2 screening, 96 samples in less than 60 minutes
High throughput HEp-2 screening, 96 samples in less than 60 minutes
The antigen on the ANA / AMA immunoblot is a nuclear extract from HEp 2 cells (enriched with cytoplasmic proteins).
The antigen on the ANA / AMA immunoblot is a nuclear extract of HEp 2 Cells (enriched with cytoplasmic proteins).
IIF on HEp-2 (punctate staining pattern throughout the nucleus; only the nucleolar regions are generally unstained).
IIF with HEp-2 (Dotted staining pattern throughout the nucleus; only the nucleolar regions are generally not stained).
The method of claim 10 wherein said culture cells are HEp-2 cells which are cultured in the absence of microcarriers.
The method of claim 10 wherein the culture cells are are HEp-2 cellsgrown in the absence of microcarriers.
As a standard for routine diagnosis, parallel tests should be carried out on both tissue sections and HEp-2 cells, since some antibodies react differently in each of these systems.
In routine diagnostics, parallel tests on tissue sections and HEp2 cells as some antibodies react differently in both systems.
The software is adapted to HEp-2 screening, cell counting, apoptosis assays, HLA screening and many more applications.
The software was designed for the Hep-2 Screening, counting cells, HLA screening, and much more. adapted.
Fluorescence pattern of ANA on RPE differed from the well known pattern on Hep-2 cells.
However, fluorescence patterns found on RPE differ from the Hep-2 patterns.
A compound according to claim 2 wherein the monoclonal antibody is of the IgM subtype and whose EC₅₀ of downmodulation on HEp-2 cells [ATCC No. CCL 23] is in the range of 30 ng / ml to 90 ng / ml.
A connection according to claim 2, whereby the monoclonal antibody is of the IgM subtype and its EC₅₀ of the down regulation HEp-2 Cells [ATCC No. CCL 23] is in the range of 30 ng / ml to 90 ng / ml.
Shell vials (with caps) containing healthy HEp-2 cells or other susceptible cells should be used for inoculation., 14
Shell vials (with lids) that are healthy should be used for inoculation HEp-2 cells or contain other susceptible cells., 14
The learned abstract shape models are either averaged shapes from groups of groups of objects or medians in the form of individual groups of HEp-2 cells.
The learned abstract form models are either averaged forms from groups of objects or medians as individual forms from groups of HEp-2 cells.
An immunofluorescence test on cell cultures (e.g. HEp-2 cells) identifies nuclear antigenic systems. However, this method often also detects unspecific stimulated nuclear antibodies (e.g. in case of an infection).
An immunofluorescence test on cell cultures (e.g. HEp2 cells, human epithelial cells) recognizes nuclear antigen systems. However, this method often also detects non-specifically stimulated core antibodies (e.g. in the event of an infection).
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