Mre11(Phospho-Ser676) Rabbit Polyclonal Antibody, 100ul Vessels which is characterized by severe

which is characterized by severe growth defects

CDH2 encodes a classical cadherin and member of the cadherin superfamily

Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria

HSFX2 is a Protein Coding gene

The encoded protein associates with the heat-shock protein Hsc70 and plays a role in clathrin-mediated endocytosis

Mre11(Phospho-Ser676) Rabbit Polyclonal Antibody, 100ul Vessels which is characterized by severeThis gene encodes a nuclear protein involved in homologous recombination telomere length maintenance and DNA double strand break repair. By itself the protein has 3' to 5' exonuclease activity and endonuclease activity. The protein forms a complex with the RAD50 homolog; this complex is required for nonhomologous joining of DNA ends and possesses increased single stranded DNA endonuclease and 3' to 5' exonuclease activities. In conjunction with a DNA