NFκB-p52 (Cleaved-A454) Rabbit Polyclonal Antibody, 100ul Human Genome Knockout Libraries Typing for these polymorphisms is

Typing for these polymorphisms is routinely done for bone marrow and kidney trans

Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported| with the most common allele| Ile654/Ile655| shown here

Many of the effects of laminin are mediated through interactions with cell surface receptors

The protein is an important drug target for the treatment of type 2 diabetes and stroke

Translocation t(3

NFκB-p52 (Cleaved-A454) Rabbit Polyclonal Antibody, 100ul Human Genome Knockout Libraries Typing for these polymorphisms isdisease: A chromosomal aberration involving NFKB2 is found in a case of B cell non Hodgkin lymphoma (B NHL). Translocation t(10; 14)(q24; q32) with IGHA1. The resulting oncogene is also called Lyt 10C alpha variant. disease: A chromosomal aberration involving NFKB2 is found in a cutaneous T cell leukemia (C TCL) cell line. This rearrangement produces the p80HT gene which encodes for a truncated 80 kDa protein (p80HT). disease: In B cell leukemia (B