CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CDKL3 was identified as a

CDKL3 was identified as a gene absent in leukemic patients with chromosome 5q deletion

These DNase/RNase-free tips come in a 2-20μl size

NFKB1/p105

making it ideal for Cell Culture Applications

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

CYTSA Rabbit Polyclonal Antibody, 100ul Bottles CDKL3 was identified as aThis gene encodes a coiled coil domain containing protein. The encoded protein may play a critical role in actin cytoskeletal reorganization during facial morphogenesis. Mutations in this gene are a cause of oblique facial clefting 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A read through transcript composed of SPECC1L (sperm antigen with calponin homology and coiled coil domains 1 like)