Sp2 Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene are

Defects in this gene are a cause of autosomal dominant cutis laxa

the immune response

preserving monolayer cells due to insert movement and preventing the loss of media due to capillary action

APEX1 encodes the major AP endonuclease in human cells

may interact with and regulate the activity of this kinase

Sp2 Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene areSP2 (Sp2 transcription factor) encodes a member of the Sp subfamily of Sp XKLF transcription factors. Sp family proteins are sequence specific DNA binding proteins characterized by an amino terminal trans activation domain and three carboxy terminal zinc finger motifs. This protein contains the least conserved DNA binding domain within the Sp subfamily of proteins, and its DNA sequence specificity differs from the other Sp proteins. It localizes