HXB3 Polyclonal Antibody, 20ul Liquid Handling ＆Storage also known as Simpson dysmorphia

also known as Simpson dysmorphia syndrome

Capacity：50mL x 4 Diameter×depth：29

|The C-terminus of p100 might be involved in cytoplasmic retention| inhibition of DNA-binding by p52 homodimers| and/or transcription activation

oculoleptomeningeal amyloidosis

HXB3 Polyclonal Antibody, 20ul Liquid Handling ＆Storage also known as Simpson dysmorphiaThis gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence specific transcription factor that is involved in development. Increased expression of this gene is associated with a distinct biologic subset of acute myeloid leukemia (AML).