Fli-1 Polyclonal Antibody, 100ul Dialysis Deletion or mutation of this

Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders

It is localized in nuclear bodies of the nucleus

Online Calibration: The DLAB pipette can be calibrated online via the official website

ROBO3 lacks motif CC1

Fli-1 Polyclonal Antibody, 100ul Dialysis Deletion or mutation of thisFLI1 encodes friend leukemia integration 1 transcription factor containing an ETS DNA binding domain. FLI1 can undergo a t (11; 22) (q24; q12) translocation with the Ewing sarcoma gene on chromosome 22, which results in a fusion gene that is present in the majority of Ewing sarcoma cases. An acute lymphoblastic leukemia associated t (4; 11) (q21; q23) translocation involving this gene has also been identified. Alternative splicing results in multiple