Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
TTBK2 encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Additionally we are shipping TTBK2 Antibodies (77) and TTBK2 Proteins (7) and many more products for this protein.
Showing 1 out of 6 products:
Study shows that TTBK2 is a dedicated regulator of the initiation of ciliogenesis in vivo; TTBK2 acts at the distal end of the basal body, where it promotes the removal of CP110, which caps the mother centriole, and promotes recruitment of intraflagellar transport proteins.
Our findings suggest a possible etiology for the two most common frontotemporal lobar degeneration subtypes through a TTBK1/2 activation driven mechanism of neurodegeneration
Enhanced expression of circ-TTBK2 promoted cell proliferation, migration, and invasion, while inhibited apoptosis in glioma cells.
TTBK2 down-regulates GluK2 activity by decreasing the receptor protein abundance in the cell membrane via RAB5-dependent endocytosis.
TTBK1/2 kinases may represent attractive targets for therapeutic intervention for TDP-43 proteinopathies such as Amyotrophic lateral sclerosis and Frontotemporal lobar degeneration-TDP.
TTBK2 is a multifunctional kinase involved in important cellular processes and demands augmented efforts in investigating its functions
TTBK2 phosphorylates KIF2A and antagonizes KIF2A-induced depolymerization at microtubules plus ends for cell migration.
TTBK2 bound EB1 and Cep164 through its SxIP motifs and a proline-rich motif, respectively.
data suggest that TTBK2 also acts upstream of Cep164, contributing to the assembly of distal appendages
Dominant truncating mutations in human TTBK2 cause spinocerebellar ataxia type 11 (SCA11); these mutant proteins do not promote ciliogenesis and inhibit ciliogenesis in wild-type cells.
TTBK2 is a completely novel regulator of Na(+)-coupled glucose transport.
findings reveals a major role of PRKX, TTBK2 and RSK4 in triggering Sunitinib resistance formation; data suggest transcriptional regulation of these kinases together with other proteins might play an important role in formation of Sunitinib resistance by affecting transcription factors
two-basepair deletion (c.1306_1307delGA, p.D435fs448X in exon 12) lead to a premature stop codon in the TTBK2 gene; spinocerebellar ataxia patients had phenotypic of slowly progressive almost pure cerebellar ataxia with normal life expectancy
Examination the TTBK2 gene in 68 unrelated spinocerebellar ataxia patients displayed the normal elution profile, which denoted that no disease-related mutation was identified. We provided the evidence that SCA11 is a rare form of ataxia in China.
These data suggest that TTBK2 is important in the tau cascade and in spinocerebellar degeneration.
that SCA11 is an extremely rare cause for dominantly inherited ataxias (TTBK2) in the German population.
This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11)\; a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.
tau tubulin kinase 2
, tau-tubulin kinase 2
, protein bartleby
, tau tubulin kinase 1