HXA11 Polyclonal Antibody, 100ul Gene Editing a region associated with Cornelia

a region associated with Cornelia de Lange syndrome

subcellular location:Associated with the endoplasmic reticulum and nuclear

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

and higher expression of this gene may be correlated with shorter survival time in lung cancer patients

have similar tissue specificities

HXA11 Polyclonal Antibody, 100ul Gene Editing a region associated with CorneliaIn vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved