SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts protein tyrosine kinase 2 beta

protein tyrosine kinase 2 beta undergoes rapid tyrosine phosphorylation and activation in response to increases in the intracellular calcium concentration

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Alterations in this region may be associated with the Beckwith-Wiedemann syndrome

but also play a role in other tissues such as bone

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

SOLH2 Rabbit Polyclonal Antibody, 20ul Culture Plate Inserts protein tyrosine kinase 2 betaThis 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).