Tau Polyclonal Antibody, 20ul[BT-AP08838] Buffers & Solutions A loss of function mutation

A loss of function mutation in GPT2 has been associated with developmental encephalopathy

Designed to support the growth of CHO cells

Polymorphisms at this locus (CCL3) may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1

Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions

and overexpression of a kinase-dead version of the protein interferes with normal cell cycle progression

Tau Polyclonal Antibody, 20ul[BT-AP08838] Buffers & Solutions A loss of function mutationMAPT encodes the microtubule associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico