PRDM3 Polyclonal Antibody, 20ul Stepper GNB5 encodes a beta subunit

GNB5 encodes a beta subunit

Mutations in this gene have been associated with atherosclerosis and a higher risk of myocardial infarction

Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK)

FOXO3 likely functions as a trigger for apoptosis through expression of genes necessary for cell death

which is the product of this gene

PRDM3 Polyclonal Antibody, 20ul Stepper GNB5 encodes a beta subunitPRDM3 can be produced either as a separate transcript and as a fusion transcript with EVI1. A chromosomal aberration involving PRDM3 is found in a form of acute myeloid leukemia. The myelodysplastic syndromes (MDS, formerly known as "preleukemia") are a diverse collection of hematological conditions united by ineffective production of blood cells and varying risks of transformation to acute myelogenous leukemia.