Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing (NACC1) ELISA Kits

NACC1 encodes a member of the BTB\\/POZ protein family. Additionally we are shipping Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing Antibodies (90) and Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human NACC1 NACC1 112939 Q96RE7
Anti-Mouse NACC1 NACC1 66830 Q7TSZ8
Anti-Rat NACC1 NACC1 171454 O35260
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More ELISA Kits for Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing Interaction Partners

Human Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing (NACC1) interaction partners

  1. study presents a phenotype-genotype correlation for SCN1A (show SCN1A ELISA Kits); described a distinct SCN1A (show SCN1A ELISA Kits) phenotype, early infantile SCN1A (show SCN1A ELISA Kits) encephalopathy, which is readily distinguishable from the Dravet syndrome and genetic epilepsy with febrile seizures plus

  2. 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 ELISA Kits) dysfunction.

  3. this study showed that SCN1A (show SCN1A ELISA Kits) testing be considered in all individuals with febrile seizures or Dravet syndrome , as well as in familial cases consistent with febrile seizures.

  4. This study found significant differences in the distribution of truncating and missense variants across the SCN1A (show SCN1A ELISA Kits) sequence among healthy individuals, patients with Dravet syndrome.

  5. SCN1A (show SCN1A ELISA Kits) 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.

  6. The association study indicated that age at first seizure and frameshift mutations of SCN1A (show SCN1A ELISA Kits) were associated with Dravet syndrome.

  7. NAC1 forms a protein complex to function as a transcriptional regulator in cancer cells

  8. 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

  9. Study reported the range of rare copy number variants found in SCN1A (show SCN1A ELISA Kits) gene in a series of Welsh patients with childhood-onset epilepsy and intellectual disability and identified clearly or likely pathogenic CNVs in 8.8 % of the patients including 5 rare de novo deletions.

  10. Our findings suggest that SCN1A (show SCN1A ELISA Kits) mutation leads to changes in the dopamine system that may contribute to the behavioral abnormalities in DS.

Mouse (Murine) Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing (NACC1) interaction partners

  1. a sub-network of four factors, Nac1, Oct4 (show POU5F1 ELISA Kits), Tcf3 (show TCF7L1 ELISA Kits), and Sox2 (show SOX2 ELISA Kits), regulates mouse embryonic stem cell differentiation into the alternative mesendodermal and neuroectodermal fates.

  2. The interaction of Nac1 with Miz1 (show PIAS2 ELISA Kits) may thus be relevant to its mechanism of tumourigenesis in ovarian cancer.

  3. 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.

  4. 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.

  5. these data indicate involvement of NAC1 in the acute behavioral and neurochemical responses to psychomotor stimulants

  6. Nanog (show NANOG ELISA Kits) interacts with Nac1 through WNAAP to regulate the cell cycle of stem cells via the ERas/phosphatidylinositol 3-kinase/Akt (show AKT1 ELISA Kits) pathway, but not pluripotency

Nucleus Accumbens Associated 1, BEN and BTB (POZ) Domain Containing (NACC1) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with NACC1

  • nucleus accumbens associated 1, BEN and BTB (POZ) domain containing (NACC1) antibody
  • nucleus accumbens associated 1, BEN and BTB (POZ) domain containing (Nacc1) antibody
  • sodium channel, voltage-gated, type I, alpha subunit (SCN1A) antibody
  • 2010001H03Rik antibody
  • 4930511N13Rik antibody
  • BEND8 antibody
  • Btbd14b antibody
  • BTBD30 antibody
  • EIEE6 antibody
  • FEB3 antibody
  • FEB3A antibody
  • FHM3 antibody
  • GEFSP2 antibody
  • HBSCI antibody
  • Nac-1 antibody
  • Nac1 antibody
  • NACC1 antibody
  • Nav1.1 antibody
  • SCN1 antibody
  • SMEI antibody

Protein level used designations for NACC1

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 , NAC-1 , 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

GENE ID SPECIES
112939 Homo sapiens
484918 Canis lupus familiaris
525378 Bos taurus
66830 Mus musculus
171454 Rattus norvegicus
6323 Homo sapiens
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