Beta-actin Monoclonal Antibody(A02), 20ul Cell Function Analysis Mutations in PEX1 have been

Mutations in PEX1 have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy

CDC37L1 is a cytoplasmic phosphoprotein that exists in complex with HSP90 (HSPCA

apoptosis and differentiation

and mutations in this gene have been associated with congenital chloride diarrhea

TERF1 (telomeric repeat binding factor 1) encodes a telomere specific protein which is a component of the telomere nucleoprotein complex

Beta-actin Monoclonal Antibody(A02), 20ul Cell Function Analysis Mutations in PEX1 have beenThis gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, and integrity. This actin is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins.