R3378
Red blood cells from sheep
dry powder (glutaraldehyde treated)
biological source
sheep
form
dry powder (glutaraldehyde treated)
technique(s)
ELISA: suitable
storage temp.
2-8°C
Application
Red blood cells from sheep have been used to analyze T-lymphocyte dependent antibody response by ELISA. SRBCs are treated with glutaraldehyde to improve binding of the cells to the assay plate.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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A P Cutrera et al.
The Journal of experimental biology, 213(5), 715-724 (2010-02-16)
It was recently hypothesised that specific induced defences, which require substantial time and resources and are mostly beneficial against repeated infections, are more likely to be favoured in 'slow-living-pace' species. Therefore, understanding how different types of immune defences might vary
Ai Koganei et al.
Journal of immunotoxicology, 4(1), 77-82 (2008-10-30)
An enzyme-linked immunosorbent assay (ELISA) using whole sheep red blood cells (SRBC) has been reported as one of the methods for detecting a T-lymphocyte-dependent antibody response. However, it has not been widely used because of SRBC problems such as the
Murat Muradoglu et al.
Biomedical optics express, 3(10), 2465-2470 (2012-10-20)
In the context of a bioreactor, cells are sensitive to cues from other cells and mechanical stimuli from movement. The ability to provide the latter in a discrete fluidic system presents a significant challenge. From a prior finding that the
Louis T McLane et al.
Biophysical journal, 104(5), 986-996 (2013-03-12)
A voluminous polymer coat adorns the surface of many eukaryotic cells. Although the pericellular matrix (PCM) often extends several microns from the cell surface, its macromolecular structure remains elusive. This massive cellular organelle negotiates the cell's interaction with surrounding tissue
Matthew A Inlay et al.
Journal of immunology (Baltimore, Md. : 1950), 177(2), 1146-1151 (2006-07-05)
Somatic hypermutation (SHM) of the rearranged Ig genes is required for the affinity maturation of Abs. SHM is almost exclusively targeted to the rearranged Ig loci, but the mechanism of this gene-specific targeting remains unclear. The Ig kappa L chain
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