|Western Blot (WB)||0.3-1.0 ug/ml|
|Tested Species reactivity||Human|
|Host / Isotype||Goat / IgG|
|Immunogen||Synthetic peptide sequence (HLKTQAEQLHNH) corresponding to the C-terminus amino acids of TAZ|
|Purification||Antigen affinity chromatography|
|Storage buffer||TBS, pH 7.3, with 0.5% BSA|
|Contains||0.02% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
This antibody is predicted to react with canine, mouse and rat based on sequence homology.
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 , hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction . 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: BTHS; cardiomyopathy, dilated 3A (X-linked); CMD3A; EFE2; FLJ27390; G4.5; HGNC:11577; LVNCX; OTTHUMP00000061673; Protein G4.5; Tafazzin; tafazzin (cardiomyopathy, dilated 3A (X-linked) endocardial fibroelastosis 2 Barth syndrome); TAZ; Taz1; XX-FW83563B9.3
Gene Aliases: BTHS; CMD3A; EFE; EFE2; G4.5; LVNCX; TAZ; Taz1
UniProt ID: (Human) Q16635
Entrez Gene ID: (Human) 6901
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