Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
NACC1 encodes a member of the BTB/POZ protein family. Additionally we are shipping Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing Proteins (3) and many more products for this protein.
Showing 10 out of 60 products:
Human Monoclonal NACC1 Primary Antibody for EIA, IHC (p) - ABIN1108376
Korutla, Wang, Lewis, Neustadter, Stromberg, Mackler: Differences in expression, actions and cocaine regulation of two isoforms for the brain transcriptional regulator NAC1. in Neuroscience 2002
Show all 2 references for ABIN1108376
Human Monoclonal NACC1 Primary Antibody for IHC, ELISA - ABIN969307
Beausoleil, Jedrychowski, Schwartz, Elias, Villén, Li, Cohn, Cantley, Gygi: Large-scale characterization of HeLa cell nuclear phosphoproteins. in Proceedings of the National Academy of Sciences of the United States of America 2004
Cow (Bovine) Polyclonal NACC1 Primary Antibody for WB - ABIN2775934
Yeasmin, Nakayama, Ishibashi, Katagiri, Iida, Purwana, Nakayama, Miyazaki: Expression of the bric-a-brac tramtrack broad complex protein NAC-1 in cervical carcinomas seems to correlate with poorer prognosis. in Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Dog (Canine) Polyclonal NACC1 Primary Antibody for WB - ABIN374830
Wang, Rao, Chu, Shen, Levasseur, Theunissen, Orkin: A protein interaction network for pluripotency of embryonic stem cells. in Nature 2006
Cow (Bovine) Polyclonal NACC1 Primary Antibody for IHC, WB - ABIN2775909
Ota, Suzuki, Nishikawa, Otsuki, Sugiyama, Irie, Wakamatsu, Hayashi, Sato, Nagai, Kimura, Makita, Sekine, Obayashi, Nishi, Shibahara, Tanaka, Ishii, Yamamoto, Saito, Kawai, Isono, Nakamura, Nagahari et al.: Complete sequencing and characterization of 21,243 full-length human cDNAs. ... in Nature genetics 2003
No causative variants were identified in any of non-DS epileptic patients in our cohort, suggesting a minor, but not irrelevant role for SCN1A (show SCN1A Antibodies) in patients with other types of childhood epilepsy.
Mutations in SCN1A (show SCN1A Antibodies) and SCN2A (show SCN2A Antibodies) are a predisposing factor of acute encephalopathy with biphasic seizures and late reduced diffusion
Evaluation of Presumably Disease Causing SCN1A (show SCN1A Antibodies) Variants in a Cohort of Common Epilepsy Syndromes.
The SCN1A (show SCN1A Antibodies) IVS5-91G>A SNP is associated with susceptibility to epilepsy. SNPs in EPHX1 (show EPHX1 Antibodies) gene are influencing CBZ metabolism and disposition
Human Nav1.6 (show SCN8A Antibodies) channels generate larger resurgent currents than human Nav1.1 (show SCN1A Antibodies) channels, but the SCN4B (show SCN4B Antibodies)-derived Navbeta4 (show SCN4B Antibodies) peptide does not protect either isoform from use-dependent reduction.
NAC1 has potential as a marker for distinguishing OED from CIS (show CISH Antibodies)/OSCC
We report the association of two novel homozygous missense mutations of the SCN1A (show SCN1A Antibodies) gene in four children with infantile epilepsies from two consanguineous pedigrees
This study provide the evidence SCN1A (show SCN1A Antibodies) mutation releate to Autism Spectrum Disorder.
Molecular genetic testing detected a de novo SCN1A (show SCN1A Antibodies) gene deletion in heterozygous form, and revealed SCN1A (show SCN1A Antibodies) gene associated monogenic epileptic syndrome being in the genetic background of therapy-resistant seizures.
Combining the TALEN and iPSC methods, we developed two iPS (show SLC27A4 Antibodies) cell lines by generating the point mutation A5768G in the SCN1A (show SCN1A Antibodies) gene, which encodes the voltage-gated sodium channel Nav1.1 (show SCN1A Antibodies) alpha subunit (show POLG Antibodies).
The interaction of Nac1 with Miz1 (show PIAS2 Antibodies) may thus be relevant to its mechanism of tumourigenesis in ovarian cancer.
NAC1 participates in the motility and differentiation of developing chondrocytes and cartilaginous tissues, and its expression is necessary to maintain normal axial patterning of murine skeleton.
The mouse Nac1 gene consist of six exons, with exon 2 containing an alternative splice donor, providing a molecular explanation of the splice variants observed in mouse and rat.
these data indicate involvement of NAC1 in the acute behavioral and neurochemical responses to psychomotor stimulants
Nanog (show NANOG Antibodies) interacts with Nac1 through WNAAP to regulate the cell cycle of stem cells via the ERas/phosphatidylinositol 3-kinase/Akt (show AKT1 Antibodies) pathway, but not pluripotency
The vertebrate sodium channel is a voltage-gated ion channel essential for the generation and propagation of action potentials, mainly in nerve and muscle. Voltage-sensitive sodium channels are heteromeric complexes consisting of a large central pore-forming glycosylated alpha subunit, and two smaller auxiliary beta subunits. This gene encodes the large alpha subunit, and mutations in this gene have been associated with several epilepsy, convulsion and migraine disorders. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript.
BEN domain containing 8
, BTB/POZ domain-containing protein 14B
, nucleus accumbens-associated protein 1
, transcriptional repressor NAC1
, nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
, BTB (POZ) domain containing 14B
, nucleus accumbens-1
, sodium channel protein type 1 subunit alpha
, sodium channel protein type I subunit alpha
, sodium channel protein, brain I alpha subunit
, sodium channel voltage gated type 1 alpha subunit
, sodium channel, voltage-gated, type I, alpha polypeptide
, voltage-gated sodium channel subunit alpha Nav1.1