MRGRD Polyclonal Antibody, 50ul Molecular Biology Mutations in SPTAN1 are the

Mutations in SPTAN1 are the cause of early infantile epileptic encephalopathy-5

MIM 605977) are the catalytic subunits of the IMP complex (Burri et al

The protein encoded by E2F4 is a member of the E2F family of transcription factors

This gene encodes a protein that belongs to a family of helicases that are involved in the ATP-dependent unwinding of nucleic acid duplexes

Homotetramers consisting of a proteolytically cleaved form of the protein| or type A subunit| exhibit low affinity for heparin and do not interact with the ECM

MRGRD Polyclonal Antibody, 50ul Molecular Biology Mutations in SPTAN1 are theMay regulate nociceptor function and or development, including the sensation or modulation of pain. Functions as a specific membrane receptor for beta alanine. Beta alanine at micromolar doses specifically evoked Ca(2+) influx in cells expressing the receptor. Beta alanine decreases forskolin stimulated cAMP production in cells expressing the receptor, suggesting that the receptor couples with G protein G(q) and G(i).,Belongs to the G protein coupled