Purification and biochemical analysis of antigen-specific suppressor factors isolated from T-cell hybridomas. 1982

D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder

UI MeSH Term Description Entries
D008222 Lymphokines Soluble protein factors generated by activated lymphocytes that affect other cells, primarily those involved in cellular immunity. Lymphocyte Mediators,Mediators, Lymphocyte
D005796 Genes A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms. Cistron,Gene,Genetic Materials,Cistrons,Genetic Material,Material, Genetic,Materials, Genetic
D006825 Hybridomas Cells artificially created by fusion of activated lymphocytes with neoplastic cells. The resulting hybrid cells are cloned and produce pure MONOCLONAL ANTIBODIES or T-cell products, identical to those produced by the immunologically competent parent cell. Hybridoma
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000941 Antigens Substances that are recognized by the immune system and induce an immune reaction. Antigen
D012333 RNA, Messenger RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm. Messenger RNA,Messenger RNA, Polyadenylated,Poly(A) Tail,Poly(A)+ RNA,Poly(A)+ mRNA,RNA, Messenger, Polyadenylated,RNA, Polyadenylated,mRNA,mRNA, Non-Polyadenylated,mRNA, Polyadenylated,Non-Polyadenylated mRNA,Poly(A) RNA,Polyadenylated mRNA,Non Polyadenylated mRNA,Polyadenylated Messenger RNA,Polyadenylated RNA,RNA, Polyadenylated Messenger,mRNA, Non Polyadenylated
D013491 Suppressor Factors, Immunologic Proteins, protein complexes, or glycoproteins secreted by suppressor T-cells that inhibit either subsequent T-cells, B-cells, or other immunologic phenomena. Some of these factors have both histocompatibility (I-J) and antigen-specific domains which may be linked by disulfide bridges. They can be elicited by haptens or other antigens and may be mass-produced by hybridomas or monoclones in the laboratory. Immunologic Suppressor Factors,Suppressor T-Cell Factors,T-Cell Suppressive Factors,T-Suppressor Factors,Factors, Immunologic Suppressor,Factors, T Suppressor,Suppressor Factor (SF4),T Cell Suppressor Factors,Factors, Suppressor T-Cell,Factors, T-Cell Suppressive,Factors, T-Suppressor,Suppressive Factors, T-Cell,Suppressor Factors, T,Suppressor T Cell Factors,T Cell Suppressive Factors,T Suppressor Factors,T-Cell Factors, Suppressor
D013601 T-Lymphocytes Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen. T Cell,T Lymphocyte,T-Cells,Thymus-Dependent Lymphocytes,Cell, T,Cells, T,Lymphocyte, T,Lymphocyte, Thymus-Dependent,Lymphocytes, T,Lymphocytes, Thymus-Dependent,T Cells,T Lymphocytes,T-Cell,T-Lymphocyte,Thymus Dependent Lymphocytes,Thymus-Dependent Lymphocyte
D014176 Protein Biosynthesis The biosynthesis of PEPTIDES and PROTEINS on RIBOSOMES, directed by MESSENGER RNA, via TRANSFER RNA that is charged with standard proteinogenic AMINO ACIDS. Genetic Translation,Peptide Biosynthesis, Ribosomal,Protein Translation,Translation, Genetic,Protein Biosynthesis, Ribosomal,Protein Synthesis, Ribosomal,Ribosomal Peptide Biosynthesis,mRNA Translation,Biosynthesis, Protein,Biosynthesis, Ribosomal Peptide,Biosynthesis, Ribosomal Protein,Genetic Translations,Ribosomal Protein Biosynthesis,Ribosomal Protein Synthesis,Synthesis, Ribosomal Protein,Translation, Protein,Translation, mRNA,mRNA Translations
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
April 1988, Cellular immunology,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
August 1981, Immunology,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
January 1978, Current topics in microbiology and immunology,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
January 1981, International archives of allergy and applied immunology,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
July 1979, European journal of immunology,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
December 1983, Journal of immunology (Baltimore, Md. : 1950),
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
July 1990, Journal of immunology (Baltimore, Md. : 1950),
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
August 1984, Hospital practice (Office ed.),
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
April 1989, Hybridoma,
D R Webb, and B A Araneo, and C Healy, and J A Kapp, and K Krupen, and I Nowowiejski, and C W Pierce, and C M Sorensen, and S Stein, and K J Wieder
January 2000, Advances in immunology,
Copied contents to your clipboard!