TAFAZZIN/TAZ Target & Gene Products-cDNA ORF clones/siRNA/antibody/protein

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Target sublocation: Introcelluar Protein.
This gene encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in this gene 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 produced; the short form lacks a hydrophobic leader sequence and may exist as a cytoplasmic protein rather than being membrane-bound. Other alternatively spliced transcripts have been described but the full-length nature of all these transcripts is not known. [provided by RefSeq, Jul 2008]

Pre-made viral vector of TAFAZZIN/TAZ cDNA Clones/ORF Plasmid

TAFAZZIN/TAZ siRNA/miRNA/oligo for RNA interfence (RNAi)

TAFAZZIN/TAZ antibody/GMab

TAFAZZIN/TAZ recombinant protein