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DCDC2 encodes a doublecortin domain-containing family member. Additionally we are shipping DCDC2 Proteins (5) and many more products for this protein.
Showing 10 out of 96 products:
Human Polyclonal DCDC2 Primary Antibody for IF (p), IHC (p) - ABIN1385734
Choi, de Poot, Lee, Kim, Han, Kim, Finley, Lee: Open-gate mutants of the mammalian proteasome show enhanced ubiquitin-conjugate degradation. in Nature communications 2016
Human Polyclonal DCDC2 Primary Antibody for ELISA, IHC - ABIN251255
Cope, Harold, Hill, Moskvina, Stevenson, Holmans, Owen, ODonovan, Williams: Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. in American journal of human genetics 2005
Mouse (Murine) Polyclonal DCDC2 Primary Antibody for ELISA, WB - ABIN251687
McGrath, Smith, Pennington: Breakthroughs in the search for dyslexia candidate genes. in Trends in molecular medicine 2006
Human Polyclonal DCDC2 Primary Antibody for ICC, IF - ABIN4304490
Jeruschke, Jeruschke, DiStasio, Karaterzi, Büscher, Nalbant, Klein-Hitpass, Hoyer, Weiss, Stottmann, Weber: Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression. in PLoS ONE 2015
Study identified biallelic missense mutations or in-frame deletion in DCDC2 in children affected with neonatal sclerosi. Mutations involve highly conserved amino acids in the doublecortin (show DCX Antibodies) domains of the protein. In cholangiocytes, DCDC2 protein is normally located in the cytoplasm and cilia, whereas in patients the mutated protein is accumulated in the cytoplasm, absent from cilia, and associated with ciliogenesis defect.
Developmental dyslexia genetic (DCDC2) and environmental factors (smoke and miscarriage) underlie ADHD traits supporting a potential pleiotropic effect.
that endogenous DYX1C1 (show DYX1C1 Antibodies) localizes to the base of the cilium, whereas DCDC2 localizes along the entire axoneme of the cilium
DCDC2 Polymorphism is associated with reading disability.
off-target, non-immune mediated effects of the mTOR (show FRAP1 Antibodies)-inhibitor everolimus on the podocyte cytoskeleton might involve regulation of microtubules, revealing a potential novel role of TUBB2B (show TUBB2B Antibodies) and DCDC2 in glomerular podocyte development
This study demonstrated that DCDC2 intron 2 deletion impair illusory visual motion perception-specifically processed by the magnocellular-dorsal (M-D) stream-is impaired in children with Developmental dyslexia.
A nonsynonymous polymorphism in DCDC2 (corrected P = 0.002) and a noncoding variant in S100B (show S100B Antibodies) (corrected P = 0.016) showed a significant association with spelling performance in families of German origin.
Our results reveal DCDC2a to be a deafness gene and a player in hair cell kinocilia and supporting cell (show PTPRJ Antibodies) primary cilia length regulation likely via its role in microtubule formation and stabilization.
the association of DCDC2 and KIAA0319 (show KIAA0319 Antibodies) with Developmental dyslexia in Chinese population should be further validated
In a population carrying a deletion in the DCDC2 gene, impaired motion perception was identified in subjects with dyslexia.
Behavioral results revealed deficits in rapid auditory processing, working memory and reference memory in Dcdc2(del2/del2) mice when compared with matched wild types.
Results link the function of the dyslexia-associated gene Dcdc2 to spike timing through activity of N-methyl-D-aspartate receptor (show GRIN1 Antibodies) (NMDAR (show GRIN1 Antibodies))
These results indicate that Dcdc2 is not required for neurogenesis, neuronal migration or differentiation in mice, but may have partial functional redundancy with doublecortin (show DCX Antibodies).
heterozygous and homozygous mutations of Dcdc2 result in persistent visuo-spatial memory deficits, as well as visual discrimination and long-term memory deficits
This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
doublecortin domain containing 2
, doublecortin domain-containing protein 2
, doublecortin domain-containing protein 2-like