Integrin beta 1(Phospho Tyr795) Polyclonal Antibody, 50ul In vitro Transcription disease:A chromosomal aberration involving FOXO3

disease:A chromosomal aberration involving FOXO3 is found in secondary acute leukemias

Defects in HCCS are a cause of microphthalmia syndromic type 7 (MCOPS7)

Accumulation of EXPAND1/MUM1 at damaged DNA sites is thought to modify the structure of the chromatin and allow access to other DNA repair factors

With the ability to store at 2-8℃ for maximum stability

Requires p18 NF-E2 for binding to the NF-E2 motif

Integrin beta 1(Phospho Tyr795) Polyclonal Antibody, 50ul In vitro Transcription disease:A chromosomal aberration involving FOXO3Integrins are heterodimeric proteins made up of alpha and beta subunits. At least 18 alpha and 8 beta subunits have been described in mammals. Integrin family members are membrane receptors involved in cell adhesion and recognition in a variety of processes including embryogenesis, hemostasis, tissue repair, immune response and metastatic diffusion of tumor cells. This gene encodes a beta subunit. Multiple alternatively spliced transcript variants