Titlebook: Leukocyte Typing II; Volume 2 Human B Lym Ellis L. Reinherz,Barton F. Haynes,Irwin D. Bernst Conference proceedings 1986 Springer-Verlag Ne

ligature

闲逛

明确

Pathogen

Use of Two Monoclonal Anti-Human B Cell Antibodies in the Study of Early B Cell Differentiationsewhere (1). Briefly somatic cell hybridization and growth of hybridomas UL-38 and UL-90 was performed essentially as described by Köhler and Milstein (2). As fusion partners PAI-O BALB/c myeloma cells (3), a nonproducing subclone of the mouse myeloma cell P3x63Ag8, were used (obtained from Dr. J.W.

Resistance

Characterization of a Human B Lymphocyte-Specific Antigen Defined by Monoclonal Antibodies HD6 and Hbrane immunoglobulin (1). Together with some non-lineage restricted cell surface markers including HLA-class II antigen, the receptor of the Fc portion of IgG, the complement component C3 receptor, and others, several distinct stages of differentiation from the pluripotent stem cell via the mature B

Induction

Six Distinct Antigen Systems of Human B Cells as Defined by Monoclonal Antibodies, Ia-like antigens, and receptors for immunoglobulin Fc (FcR) and complement C3 (CR). In recent years, a number of cell surface markers, either specific for or associated with human B cells, have also been identified using monoclonal antibodies (mAbs) to delineate human B cell development (1).

Permanent

平躺

Human B Cells: Is FMC7 a Marker for Relatively Mature B Cells or Does It Define a Population Equivaltions. These distinct cells derive from common progenitors, but cannot be converted from one subset to the other. Thus the differentiation pathway may be said to fork into parallel paths. Does the B cell lineage also fork into parallel pathways, or are all the different phenotypes which can be obser

使乳化

治愈

Human B Cell Surface Molecules Defined by an International Workshop Panel of Monoclonal Antibodies of monoclonal antibodies (mAbs) which have a similar specificity and react with the same biochemically defined antigen. The antigens detected by the First Workshop panel were identified by immunoprecipitation and PAGE gel analysis (1,2); assignment of antibodies to specific groups was also possible