EphA7 Polyclonal Antibody, 50ul[BT-AP03002] Reservoirs Defects in this gene are

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

Loss of expression of the related gene in mouse affects coat and eye pigmentation

HIST1H2BA is intronless and encodes a replication-dependent histone that is a testis/sperm-specific member of the histone H2B family

such as HIV-1: acts by inhibiting an early step of viral infection

This gene encodes a member of the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins

EphA7 Polyclonal Antibody, 50ul[BT-AP03002] Reservoirs Defects in this gene areEPHA7 belongs to the ephrin receptor subfamily of the protein tyrosine kinase family. EPH and EPH related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their