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Tafazzin Polyclonal Antibody, 20ul Enzymes & Activity Assays HIST1H2AI is intronless and encodes

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Tafazzin Polyclonal Antibody, 20ul Enzymes & Activity Assays HIST1H2AI is intronless and encodesTAZ (tafazzin) encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in TAZ have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is

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Description

HIST1H2AI is intronless and encodes a replication-dependent histone that is a member of the histone H2A family

one in the cytoplasm and one in the mitochondria

Both the human and orthologous mouse genes have been reported to encode two isoforms (with preferential cellular localization) resulting from the use of alternative in-frame translation initiation codons

TPD52L3 (tumor protein D52 like 3) encodes a member of the tumor protein D52-like family of proteins

the DHJHC m-protein or the p55 chain

Tafazzin Polyclonal Antibody, 20ul Enzymes & Activity Assays HIST1H2AI is intronless and encodesTAZ (tafazzin) encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in TAZ have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is

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