Bcl-6 (Acetyl Lys379) Rabbit Polyclonal Antibody, 50ul Hepatocytes Defects in this gene can

Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision

Contains 1 Ig-like C2-type (immunoglobulin-like) domain

Aberrant expression of CDX2 is associated with intestinal inflammation and tumorigenesis

where it constitutes the Yt blood group antigen

Bcl-6 (Acetyl Lys379) Rabbit Polyclonal Antibody, 50ul Hepatocytes Defects in this gene candisease: A chromosomal aberration involving BCL6 may be a cause of a form of B cell leukemia. Translocation t(3; 11)(q27; q23) with POU2AF1 OBF1. disease: A chromosomal aberration involving BCL6 may be a cause of lymphoma. Translocation t(3; 4)(q27; p11) with ARHH TTF. disease: Chromosomal aberrations involving BCL6 may be a cause of B cell non Hodgkin lymphoma. Translocation t(3; 14)(q27; q32); translocation t(3; 22)(q27; q11) with immunoglobulin