Tau Polyclonal Antibody, 100ul[BT-AP08844] Cytokines This suggests that the human

This suggests that the human gene is therefore a pseudogene

Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus

Defects in PARK7 are the cause of autosomal recessive early-onset Parkinson disease 7

which are typical of the ADAMTS family

The encoded protein has four extracellular C2-type immunoglobulin domains

Tau Polyclonal Antibody, 100ul[BT-AP08844] Cytokines This suggests that the humanMAPT 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