Chimaeric mice were generated by standard protocols.

Luckily the Unitarian Church had a big open space in the basement, and here is where we and our chimaeric partners fit ourselves together.

THP-1 cells bound to these chimaeric proteins, and binding was blocked by the anti-LFA-1 antibody 38.

All chimaeric fusions and inserts generated by PCR were verified by DNA sequencing.

Hagberg H, Lundholm L: Rituximab, a chimaeric anti-CD20 monoclonal antibody, in the treatment of hairy cell leukaemia.

Downing JR: The AML1-ETO chimaeric transcription factor in acute myeloid leukaemia: biology and clinical significance.

The problem presented by the uniform morphology of conventionally stained mouse chromosomes in the recognition of chimaeric or mosaic conditions can be overcome by using marker chromosomes to label cells.

Nonviral proteins have been incorporated into viral particles, for example, CD4 and chimaeric CD4-envelope proteins into avian retroviruses 12, but the displayed proteins were not shown to be folded.

In general, any experiment on the pre-implantation embryo which makes the epiblast chimaeric, even the addition of a single marked epiblast cell to the blastocyst, will result in chimaerism in each and every tissue of the fetus.

One method of constructing chimaeric (or "allophenic" ) mice is to aggregate two or more genotypically distinct morulae together and re-implant the composite embryo into the uterus of a pseudopregnant foster mother (23, and see Chapter 6, Section 2.2).

Although strategies to overcome problems with chimaeric YACs and marker-poor regions are still being worked out, it is clearly only a matter of time before a combined version of the two maps will be available to guide efforts to sequence the human genome.

In this assay, activation of the serum-response element (SRE) -LacZ reporter gene is strictly dependent on the interaction between chimaeric proteins containing the serum-response factor (SRF) DNA-binding and the VP16 transactivation domains, respectively.

The chimaeric genes were created by using polymerase chain reaction (PCR) to amplify two N-terminal domains of each ICAM, with restriction sites compatible for ligation, into an expression vector, pIg1, containing hinge, CH2 and CH3 exons of human IgG 1.

Originally, non-Ti-plasmid dependent DNA uptake was demonstrated in 1985 by R. Hain and A.P. Czernilofsky et al., in the article "Uptake, integration, expression and genetic transmission of a selectable chimaeric gene by plant protoplasts" using the Ca-phosphate coprecipitation technique.