MFRP Polyclonal Antibody, 20ul[BT-AP11304] Polyclonal Antibodies and it may be involved

and it may be involved in the differentiation of cerebellar neurons

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

ST5 was identified by its ability to suppress the tumorigenicity of Hela cells in nude mice

and its interaction with p38 decreases upon cellular stress

May mediate brain damage by nucleotides and CysLTs following ischemia

MFRP Polyclonal Antibody, 20ul[BT-AP11304] Polyclonal Antibodies and it may be involvedThis gene encodes a member of the frizzled related protein family. The encoded protein plays an important role in eye development and mutations in this gene have been associated with nanophthalmos, posterior microphthalmia, retinitis pigmentosa, foveoschisis, and optic disc drusen. The protein is encoded by a bicistronic transcript which also encodes C1q and tumor necrosis factor related protein 5 (C1QTNF5).