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STMN2 encodes a member of the stathmin family of phosphoproteins. Additionally we are shipping Stathmin-Like 2 Antibodies (106) and Stathmin-Like 2 Proteins (10) and many more products for this protein.
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Zeb (show KIAA1279 ELISA Kits)rafish studies further demonstrated an epistatic interaction between KBP and SCG10 in vivo.
Results provide a starting point for future studies that will investigate the in vivo function of SCG10 orthologues in zebrafish neural development.
RARB (show RARB ELISA Kits) and STMN2 polymorphisms were not associated with sporadic CJD (show PRNP ELISA Kits) in the Korean population.
PAK4 (show PAK4 ELISA Kits)-SCG10 signaling occurs in gastric cancer cell invasion.
STMN and SCG10 are similarly targeted by JNK (show MAPK8 ELISA Kits) but there are clear differences in JNK (show MAPK8 ELISA Kits) recognition and phosphorylation of the closely related family member, SCLIP (show STMN3 ELISA Kits).
CaMy1 via SCG10 couples Ca(2 (show CA2 ELISA Kits)+) signals with the dynamics of microtubules during neuronal outgrowth in the developing brain.
SCG10 is upregulated in the IKAP/Elp1 (show IKBKAP ELISA Kits)-deficient familial dysautonomia cerebrum lending support to the concept that SCG10 elevation can alter the microtubule organization and dynamics
Overexpression of SCG10 is associated with Liver Fibrosis.
RGS6 (show RGS6 ELISA Kits) interacts with this protein and promotes neuronal differentiation; role of the G gamma subunit-like (GGL (show GGT5 ELISA Kits)) domain of RGS6 (show RGS6 ELISA Kits)
STMN2 is required for maintaining the anchorage-independent growth state of beta-catenin (show CTNNB1 ELISA Kits)/TCF (show HNF4A ELISA Kits)-activated hepatoma cells
activity at opposite microtubule ends may play role role in regulating growth cone microtubules; ability to promote plus end growth may facilitate microtubule extension; ability to destabilize minus ends may provide tubulin (show TUBB ELISA Kits) for net plus end elongation
Review proposes a model reconciling the microtubule regulatory properties of superior cervical ganglion protein 10 with its role as a c-Jun N-terminal kinase 1 (JNK1 (show MAPK8 ELISA Kits)) effector of regeneration.
SCG10 promotes non-amyloidogenic processing of amyloid precursor protein (show APP ELISA Kits) by facilitating its trafficking to the cell surface.
This study demonstrated that axonal injury induces a dynamic regulation of SCG10 protein levels with selective accumulation in proximal axon segments.
JNK (show MAPK8 ELISA Kits) phosphorylation targets SCG10 for degradation.
SCG10 is not directly implicated in Hirschsprung diseased evelopment
the Rarb (show RARB ELISA Kits) region of Mmu14 and Stmn2, but not Cr1 (show TDGF1 ELISA Kits) or Clu (show CLU ELISA Kits) or Picalm (show PICALM ELISA Kits) have roles in prion (show PRNP ELISA Kits) disease
These findings indicate that the phosphorylation of SCG10 by JNK1 (show MAPK8 ELISA Kits) is a fundamental mechanism that governs the transition from the multipolar stage and the rate of neuronal cell movement during cortical development.
KBP binds exclusively to microtubule associated or related proteins, specifically SCG10.
This gene encodes a member of the stathmin family of phosphoproteins. Stathmin proteins function in microtubule dynamics and signal transduction. The encoded protein plays a regulatory role in neuronal growth and is also thought to be involved in osteogenesis. Reductions in the expression of this gene have been associated with Down's syndrome and Alzheimer's disease. Alternatively spliced transcript variants have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 6.
, stathmin-like 2c
, superiorcervical ganglia, neural specific 10
, neuron-specific growth-associated protein
, neuronal growth-associated protein (silencer element)
, superior cervical ganglia, neural specific 10
, superior cervical ganglion-10 protein
, stathmin 2