GRIP2 Polyclonal Antibody, 20ul Gene Synthesis A rare microsatellite polymorphism in

A rare microsatellite polymorphism in XRCC5 is associated with cancer in patients of varying radiosensitivity

Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype

Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to TGF-beta signaling

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DNA ligase 1 functions in DNA replication

GRIP2 Polyclonal Antibody, 20ul Gene Synthesis A rare microsatellite polymorphism inPDZ 5 mediates the C terminal binding of GRIA2 and GRIA3. PDZ 6 mediates interaction with the PDZ recognition motif of EFNB1. PDZ 7 mediates interaction with CSPG4.,May play a role as a localized scaffold for the assembly of a multiprotein signaling complex and as mediator of the trafficking of its binding partners at specific subcellular location in neurons.,Belongs to the GRIP2 family.,Contains 7 PDZ (DHR) domains.,subunit: Interacts with EFNB1,