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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 92 products:
Human Monoclonal NACC1 Primary Antibody for ICC, FACS - ABIN259549
Nakayama, Nakayama, Davidson, Sheu, Jinawath, Santillan, Salani, Bristow, Morin, Kurman, Wang, Shih: A BTB/POZ protein, NAC-1, is related to tumor recurrence and is essential for tumor growth and survival. in Proceedings of the National Academy of Sciences of the United States of America 2006
Show all 11 references for 259549
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 1108376
Human Polyclonal NACC1 Primary Antibody for ELISA, WB - ABIN188846
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
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
genetic variants in 3'UTR (show UTS2R Antibodies) of SCN1A (show SCN1A Antibodies)
Among these transmissions were two likely disease-causing mutations: an SCN1A (show SCN1A Antibodies) mutation transmitted to an SUDC proband and her sibling with Dravet syndrome, as well as an SLC6A1 (show SLC6A1 Antibodies) mutation in a proband with epileptic encephalopathy.
study presents a phenotype-genotype correlation for SCN1A (show SCN1A Antibodies); described a distinct SCN1A (show SCN1A Antibodies) phenotype, early infantile SCN1A (show SCN1A Antibodies) encephalopathy, which is readily distinguishable from the Dravet syndrome and genetic epilepsy with febrile seizures plus
This study demonstrated that early-life prolonged FSs have a profound long-term impact on neuronal function and adult seizure phenotypes in a mouse model of human SCN1A (show SCN1A Antibodies) dysfunction.
this study showed that SCN1A (show SCN1A Antibodies) testing be considered in all individuals with febrile seizures or Dravet syndrome , as well as in familial cases consistent with febrile seizures.
This study found significant differences in the distribution of truncating and missense variants across the SCN1A (show SCN1A Antibodies) sequence among healthy individuals, patients with Dravet syndrome.
SCN1A (show SCN1A Antibodies) mutations may alter axonal function, causing motor neuropathy/neuronopathy. This may contribute to gait disturbance and orthopedic misalignment, which is characteristic of patients with Dravet syndrome.
The association study indicated that age at first seizure and frameshift mutations of SCN1A (show SCN1A Antibodies) were associated with Dravet syndrome.
NAC1 forms a protein complex to function as a transcriptional regulator in cancer cells
a mutation in NACC1 causes microcephaly, profound developmental delays and/or intellectual disability, cataracts, severe epilepsy including infantile spasms, irritability, failure to thrive, and stereotypic hand movements
a sub-network of four factors, Nac1, Oct4 (show POU5F1 Antibodies), Tcf3 (show TCF7L1 Antibodies), and Sox2 (show SOX2 Antibodies), regulates mouse embryonic stem cell differentiation into the alternative mesendodermal and neuroectodermal fates.
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