SOLH2 Rabbit Polyclonal Antibody, 100ul Antibody Development A point mutation in the

A point mutation in the mouse ortholog

and sterile solution for 100-1000μl volume

May act by blocking phosphorylation of NFKBIB and mediating cytoplasmic retention of p65/RELA NF-kappa-B subunit

resulting in a repulsive effect on glioma cell guidance in the developing brain

SOLH2 Rabbit Polyclonal Antibody, 100ul Antibody Development A point mutation in theThis gene encodes one of testis specific transcription factors which are essential for spermatogenesis oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis specific transcription factor SOHLH1 can form heterodimers in addition to homodimers. There is a read through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591).