SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts cell-cell signalling

cell-cell signalling

Mutations in a related gene on chromosome X cause X-linked amelogenesis imperfecta

Alternate transcription initiation sites result in two transcript variants of this gene

Members of this family contain a C-terminal DNA-binding domain with three Kruppel-like zinc fingers

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SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts cell-cell signallingThis 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).