FoxO1/3/4(Phospho Thr24/32) Polyclonal Antibody, 100ul Capsule Filter Mutations in CSH1 result in

Mutations in CSH1 result in placental lactogen deficiency and Silver-Russell syndrome

The intensity of the color reaction is directly proportional to the concentration of TNF-α in the samples

The protein encoded by this gene belongs to the natriuretic peptide family

This gene is located in a chromosomal region that was genetically linked to Parkinson disease type 11

NCOA5 (nuclear receptor coactivator 5) encodes a coregulator for the alpha and beta estrogen receptors and the orphan nuclear receptor NR1D2

FoxO1/3/4(Phospho Thr24/32) Polyclonal Antibody, 100ul Capsule Filter Mutations in CSH1 result inThis gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma.