CHD2 Polyclonal Antibody, 100ul Vessels Deficiencies in this protein's function

Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases

The protein encoded by SSTR1 (somatostatin receptor 1) is a member of the superfamily of somatostatin receptors having seven transmembrane segments

increased RB3 is a unique response protein in the stathmin-related proteins following optical nerve axotomy and RB3 may be a critical target for neurodegenerative diseases

Caffey Disease and idiopathic osteoporosis

Mutations in this gene have been found in some patients with the CHARGE syndrome

CHD2 Polyclonal Antibody, 100ul Vessels Deficiencies in this protein's functionThe CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2 related helicase ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.