EKLF/CKLF/UKLF Polyclonal Antibody, 100ul Electronic Pipette Mutations in TMPO are associated

Mutations in TMPO are associated with dilated cardiomyopathy

surface immunoglobulin (Ig)

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Mutations in KAL1 cause the X-linked Kallmann syndrome

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EKLF/CKLF/UKLF Polyclonal Antibody, 100ul Electronic Pipette Mutations in TMPO are associatedKLF1 encodes a hematopoietic specific transcription factor that induces high level expression of adult beta globin and other erythroid genes. The zinc finger protein binds to the DNA sequence CCACACCCT found in the beta hemoglobin promoter. Heterozygous loss of function mutations in KLF1 result in the dominant In (Lu) blood phenotype.