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Sodium Channel, Voltage-Gated, Type VIII, alpha (SCN8A) ELISA Kits

SCN8A encodes a member of the sodium channel alpha subunit gene family. Additionally we are shipping SCN8A Antibodies (52) and SCN8A Proteins (11) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
SCN8A 6334 Q9UQD0
Anti-Rat SCN8A SCN8A 29710 O88420
Anti-Mouse SCN8A SCN8A 20273 Q9WTU3
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Top SCN8A ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 9.77 pg/ml 39.07-2500 pg/mL 96 Tests Log in to see 11 to 13 Days
$910.56
Details

More ELISA Kits for SCN8A Interaction Partners

Human Sodium Channel, Voltage-Gated, Type VIII, alpha (SCN8A) interaction partners

  1. the calpain-dependent cleavage of Nav1.6 channels expressed in human embryonic kidney (HEK) 293 cells caused the upregulation of I(NaP)

  2. Our study establishes SCN8A as a novel gene in which a recurrent mutation causes BFIS/ICCA, expanding the clinical-genetic spectrum of combined epileptic and dyskinetic syndromes.

  3. Human Nav1.6 channels generate larger resurgent currents than human Nav1.1 (show SCN1A ELISA Kits) channels, but the SCN4B (show SCN4B ELISA Kits)-derived Navbeta4 (show SCN4B ELISA Kits) peptide does not protect either isoform from use-dependent reduction.

  4. These data strengthen previous findings linking gain-of-function mutations of SCN8A with EIEE and demonstrate the importance of functional testing in establishing the pathogenicity of de novo mutations.

  5. Expression profiling of SCN8A and NDUFC2 (show NDUFC2 ELISA Kits) genes in colorectal carcinoma is reported. There was no NDUFC2 (show NDUFC2 ELISA Kits) differential expression in colorectal carcinoma.

  6. Epileptic encephalopathy related to mutations in the SCN8A genes.

  7. SCN8A encephalopathy presents in infancy with multiple seizure types.

  8. The results of this study suggested that SCN8A mutation cause early onset epilepsy and intellectual disability.

  9. identified the PI3K (show PIK3CA ELISA Kits)/Akt (show AKT1 ELISA Kits) pathway, the cell-cycle regulator Wee1 kinase (show WEE1 ELISA Kits), and protein kinase C (PKC (show PKC ELISA Kits)) as prospective regulatory nodes of neuronal excitability through modulation of the FGF14 (show FGF14 ELISA Kits):Nav1.6 complex.

  10. Data support the contribution of gain-of-function mutations of Nav1.6 (de novo variant p.Thr767Ile) that increase excitatory pyramidal neuron excitability

Mouse (Murine) Sodium Channel, Voltage-Gated, Type VIII, alpha (SCN8A) interaction partners

  1. the presences of Nav1.1 (show SCN1A ELISA Kits), Nav1.6, Navbeta1 and Navbeta3 mRNA and their reduced levels in rat SAN during aging.

  2. This study demonstrates that Nav channel expression in lumbar motoneurons is altered after SCI, and it shows a tight relationship between the calpain-dependent proteolysis of Nav1.6 channels, the upregulation of I(NaP (show CTNNBL1 ELISA Kits)) and spastici

  3. the role of Nav1.6 in general anesthesia using two mouse mutants with reduced activity of Nav1.6, was examined.

  4. observed increased hippocampal pyramidal cell excitability in heterozygous and homozygous Scn8a-R1627H mutants, and decreased interneuron excitability in heterozygous Scn8a-R1627H mutants.

  5. The data support a model where ankyrinG (show ANK3 ELISA Kits)-binding is required for preferential Nav1.6 insertion into the axon initial segment plasma membrane during development.

  6. the degenerating muscle mutation is a loss of function mutation of scn8a

  7. N1768D mutation of SCN8A is sufficient to induce seizures and SUDEP in knock-in mice.

  8. APP (show APP ELISA Kits) enhances Nav1.6 sodium channel cell surface expression through a Go-coupled JNK (show MAPK8 ELISA Kits) pathway

  9. This study provided evidence for a direct link between sodium channel activity and modulation of Rac1 and ERK1/2 (show MAPK1/3 ELISA Kits) activation in ATP-stimulated microglia, possibly by regulating Ca(2 (show CA2 ELISA Kits)+) transients

  10. results identify the hippocampus as an important structure in the mediation of Scn8a-dependent seizure protection and suggest that selective targeting of Scn8a activity might be efficacious in patients with epilepsy.

SCN8A Antigen Profile

Antigen Summary

This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with mental retardation, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.

Gene names and symbols associated with SCN8A

  • sodium channel, voltage gated, type VIII, alpha subunit (SCN8A) antibody
  • sodium channel, voltage gated, type VIII, alpha subunit (Scn8a) antibody
  • sodium channel, voltage-gated, type VIII, alpha (Scn8a) antibody
  • AI853486 antibody
  • C630029C19Rik antibody
  • CERIII antibody
  • CIAT antibody
  • dmu antibody
  • EIEE13 antibody
  • med antibody
  • mnd-2 antibody
  • mnd2 antibody
  • NaCh6 antibody
  • Nav1.6 antibody
  • nmf2 antibody
  • nmf58 antibody
  • nmf335 antibody
  • nur14 antibody
  • PN4 antibody
  • seal antibody

Protein level used designations for SCN8A

hNa6/Scn8a voltage-gated sodium channel , sodium channel protein type 8 subunit alpha , voltage-gated sodium channel subunit alpha Nav1.6 , Na+ channel , PN4 , naCh6 , peripheral nerve protein type 4 , sodium channel 6 , sodium channel protein type VIII subunit alpha , sodium channel voltage-gated type VIII alpha polypeptide , sodium channel, voltage-gated, type 8, alpha polypeptide , sodium channel, voltage-gated, type 8, alpha subunit , sodium channel, voltage-gated, type VIII, alpha polypeptide , ataxia 3

GENE ID SPECIES
6334 Homo sapiens
477604 Canis lupus familiaris
29710 Rattus norvegicus
537277 Bos taurus
20273 Mus musculus
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