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anti-Human TUBA8 Antibodies:
anti-Mouse (Murine) TUBA8 Antibodies:
anti-Rat (Rattus) TUBA8 Antibodies:
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Human Monoclonal TUBA8 Primary Antibody for ICC, FACS - ABIN969446
Abdollahi, Morrison, Sirey, Molnar, Hayward, Carr, Springell, Woods, Ahmed, Hattingh, Corry, Pilz, Stoodley, Crow, Taylor, Bonthron, Sheridan: Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia. in American journal of human genetics 2009
Show all 2 Pubmed References
Data provide evidence for a role of TUBA8 in hepatic fibrogenesis and malignancies making it a novel player in non-alcoholic steatohepatitis and hepatocellular carcinoma pathology.
TUBA8 can play a role in the regulation of cell growth, proliferation, and cell migration in a cell-specific manner in vitro.
TUBA8 is expressed at low levels in the developing human brain.
Mutation of the variant alpha-tubulin (show TUBA4A Antibodies) TUBA8 results in polymicrogyria with optic nerve hypoplasia.
Tuba8 is expressed at low levels in the developing mouse brain.
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.
alpha 4 tubulin
, tubulin alpha-4 chain
, tubulin, alpha 8
, tubulin alpha chain-like 2
, tubulin alpha-8 chain
, alpha tubulin 8
, alpha-tubulin 8
, 3,2-trans-enoyl-CoA isomerase
, L-3-hydroxyacyl-CoA dehydrogenase
, L-bifunctional protein, peroxisomal
, enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase
, peroxisomal bifunctional enzyme
, peroxisomal enoyl-CoA hydratase
, tubulin alpha 8 L homeolog