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LYAG Rabbit Polyclonal Antibody, 100ul Culture Media such as pyrimidine-4-aldehyde

SKU: 29203256752

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LYAG Rabbit Polyclonal Antibody, 100ul Culture Media such as pyrimidine-4-aldehydeThis gene encodes lysosomal alpha glucosidase which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II also known as Pompe's disease which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in

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Description

such as pyrimidine-4-aldehyde

Polymorphisms in the promoter of this gene are associated with defects in bile acid synthesis

This gene is a member of the dedicator of cytokinesis (DOCK) family and encodes a protein with a DHR-1 (CZH-1) domain| a DHR-2 (CZH-2) domain and an SH3 domain

Potassium voltage-gated channel subfamily C member 4 encoded by KCNC4 belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes

LYAG Rabbit Polyclonal Antibody, 100ul Culture Media such as pyrimidine-4-aldehydeThis gene encodes lysosomal alpha glucosidase which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II also known as Pompe's disease which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in

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