Identification of Fetal Red Blood cells after mixing with adult (75%)
and cord erythrocytes (25%)
A second application concerns monitoring the level of HbF after
treatment of sickle-cell anaemia and b-thalassemia with fetal hemoglobulin
stimulating reagents. The measurement of HbF level and the number
of cells containing fetal hemoglobin is considered to be of prognostic
value in these hemoglobinopathies and would help to evaluate the
effect of therapy.
Fetal hemoglobin can be detected by staining peripheral blood cells
with a pure or fluorochrome-labeled mouse monoclonal antibody, clone
NaM16-2F4, specific for the g chain of human Hb (1,2).
It can be used to measure a wide range of fetal cell percentages
and also in dual staining along with other hemoglobin variants and
erythrocyte surface antigens. Measurement by flow cytometry saves
time compared to traditional methods, is reproducible and gives
accurate fetal blood cell counts (3).
Specifications:
Clone NaM16-2F4, produces IgG1 immunoglobulins directed against the
human gama chain of human Hb (1,2). A protocol for use is supplied
with the purchased monoclonal antibody.
References:
1. Navenot,J-M., et al. 1997. Cytometry. 32: 186-190
2. Maier-Redelsperger, M., et al., 1994 Blood 84: 3182-3188
3. Campbell, T.A., Ware, R.E., Mason, M., 1999. Cytometry, 35, 242-248
For research only. Not for use in humans. For in vitro use only.