MFRP Polyclonal Antibody, 20ul[BT-AP11304] Polyclonal Antibodies Defects in HSPB1 are a

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

Binding to ATP mediates synaptic transmission between neurons and from neurons to smooth muscle

a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes

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and its interaction with p38 decreases upon cellular stress

MFRP Polyclonal Antibody, 20ul[BT-AP11304] Polyclonal Antibodies Defects in HSPB1 are aThis 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).