细胞功能测定

Hybridoma technology makes it possible to produce almost unlimited amounts of monospecific antibodies. Each hybridoma represents only one of several B-lymphocytes responding to a particular antigen, and for this reason, monoclonal antibodies can also be produced against impure ...

Hybrid clones will appear within 2–3 wk after fusion (see Chapter 46). It is of utmost importance that a newly established hybridoma is cloned thoroughly to ensure that the cells growing in the tissue culture are of monoclonal origin and not a mixture of two or more hybridomas. A mixture of cells may result in a ...

Two distinct populations of lymphocytes have been identified: T lymphocytes, which are thymus-dependent, and B cells, first observed in the Bursa Fabricus of birds. Mammals do not have an equivalent structure, and there are varying opinions as to the similarity of these cells between species. ...

Hybridomas are exposed to many threats, such as contamination with bacteria and fungi, loss of chromosomes coding for antibody production, overgrowth by nonsecreting mutants, and cell death resulting from overgrowth. Therefore, newly established hybridomas should be frozen and s ...

Enzyme-linked immunosorbent assay (ELISA) is a rapid and convenient method for screening of antibody producing hybridomas (1,2). The method is highly sensitive and can be applied to detect antibodies directed against soluble antigens as well as cell-bound antigens. Over a thousand cul ...

Immunodiffusion is an important qualitative method for the detection of antigens and antibodies. The technique may be used to determine the immunoglobulin heavy and light chain class and subclass of hybridoma antibodies. The monoclonal antibodies are allowed to diffuse toward anti ...

Isoelectric focusing of monoclonal antibodies in agarose gel is one of several ways to characterize a hybridoma. Isoelectric focusing is performed on each monoclonal antibody, and the mouse immunoglobulin bands are immobilized by soaking the gel with rabbit antimouse immunoglobu ...

Hybridoma technology has made possible the production of highly specific, homogeneous antibodies with predefined binding characteristics, which can be produced in large amounts, from immortal cell lines. They probably represent the immunochemist’s ideal as reagents, and mono ...

The end product of all the selection and cloning procedures described in Chapters 45–48 will be a monoclonal hybridoma culture growing in a 0.2-mL culture well. From this single well, sufficient cells must be grown for storage in liquid nitrogen. It is advisable that at least six ampules, divided bet ...

There is an increasing interest in the preparation of rat � rat hybridomas, because they have been found to be more stable in culture than mouse hybridomas and they secrete consistently high levels (10 �g/mL and above) of monoclonal antibody. In addition, certain subclasses of rat IgG have been found ...

Free GSL molecules are poorly immunogenic using conventional immunization procedures (1,2). Although immunogenicity has been increased by immunizing with purified glycolipids coated onto the surface of Salmonella minnesota organisms (3,4), this has not always been successf ...

Mycoplasma is the generic term used by cell biologists to denote organisms belonging to the Order Mycoplasmatales, which can infect cell cultures. Of particular interest are those organisms that belong to the Families Mycoplasmataceae (Mycoplasma) and Acholeplasmataceae (Ach ...

In this chapter, scale-up is described in a laboratory context (10–20 L), but the principles and techniques employed have been successfully adapted so that cells are now grown industrially in unit volumes of up to 8000 L for vaccine, interferon, and monoclonal antibody production. The need to scal ...

The ability to establish long-term B lymphocyte cultures from patients carrying particular genetic characteristics or with the ability to secrete specific antibodies (1) is an extremely valuable technique. However, there are several basic principles to follow in the approach to this ...

Prenatal diagnosis of genetic disorders associated with specific biochemical, chromosomal, or molecular characteristics can be achieved from amniotie fluid (AF) or placenta (chorionic villus: CV) samples. Chorion material is usually obtained by sampling the placenta at the imp ...

The functional cells of the blood are short-lived; they are replaced continuously by proliferation and differentiation of hematopoietic precursors. Since cell division is required, exposure to agents that destroy proliferative potential is followed by loss or reduction in blood ...

Within our field, improvement in fluorescence-activated cell sorting (FACS) and molecular technologies has led to various types of correlative studies that imply the developmental sequence and subsequent emigration of thymic-lymphocyte subsets. Unfortunately, the impli ...

In designing functional assays for the various classes of hematopoietic cells described in this book, one needs to consider the properties of the cell to be measured which must be incorporated into the assay design, and the end points to allow its specific detection. The most primitive hematopo ...

The last decade has seen major advances in our knowledge of the molecular control of hematopoiesis, widespread access to cytokines, and the development of practical assays for quantitating highly primitive hematopoietic cells. This progress has now made feasible the predictable ma ...

Under appropriate culture conditions, ES cells will spontaneously differentiate and generate colonies known as embryoid bodies (EBs) that contain precursors of multiple lineages, including those of the hematopoietic system (1–7). Previous studies have demonstrated that the m ...