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Preparation of buffered saline and determination of its osmolality. 2 Size exclusion chromatography on Superdex 75. Figure 1. Flow-chart of the construction of the operon fusion clones of human ATP1G2. (A) The recombinant plasmids pBI::ATP1G2 contains the entire human ATP1G2. (B) The recombinant plasmid pBI::ATP1G2::CAT contains the entire human ATP1G2 gene and the chloramphenicol acetyltransferase gene.

Marked cells were stained with the specific monoclonal antibodies anti-CD3, anti-CD4, and anti-CD8. The presence of T cells, B cells, and monocytes was determined on the basis of their surface staining with anti-CD3 and anti-CD4, respectively. The data show the percentage of CD4+T cells, CD8+T cells, B cells, and monocytes in the blood, and the amount of released LDH and creatine kinase (CK) to cell number ratios in each of the in vitro investigations.

A T lymphocyte is a type of lymphocyte of the immune system that is capable of secreting a variety of bioactive substances. They are characterized by small, curved, ovoid, or roughly shaped nuclei that are divided into lobes and located in the cytoplasm of the cell. This results in the typical appearance of a teardrop shape. Most T cells are activated when they recognize foreign pathogens or other foreign cells via their T cell receptors.

The antigen receptors in both B and T cells are composed of surface immunoglobulins and heterodimers of T cell receptors. The T cell receptors interact with peptide antigens that have been bound to major histocompatibility complex class II on the surface of antigen-presenting cells, and T cells therefore recognize each other and are targeted for destruction.

The major histocompatibility complex is a series of genes located on chromosomal region 6 of the human genome in the centromere-p arm of chromosome 6. The locus contains class I and class II molecules that encode for proteins of the major histoc