Epilepsy and Seizures Related Research Tools

The epilepsy is a chronic neurological disorder in which clusters of nerve cells in the brain signal abnormally and cause seizures. The syndromes include uncontrolled shaking movements (e.g. tonic-clonic seizure involving much of the body with loss of consciousness), shaking movements (e.g. focal seizure involving only part of the body with variable levels of consciousness) and subtle momentary loss of awareness (e.g. absence seizure).

Seizures can be conceptualized as a result of the imbalance between excitation (E) and inhibition (I) in the brain. The factors that alter E/I balance can be genetic or acquired. These factors vary from genes and subcellular signaling cascades to widespread neuronal circuits, such as abnormal synaptic connectivity in cortical dysplasia, abnormal GABA receptor subunits in Angelman syndrome, potassium channel mutations in Brief Fear of Negative Evaluation Scale (BFNE) and structural alteration of hippocampal circuitry following prolonged febrile seizures.

Creative Biolabs provides all kinds of products that can be applied to neuroscientific research: the roles of genes versus acquired factors in seizure predisposition, how epilepsy develops and how to prevent the consequences of seizures. Our products include neural cell lines and specialty media, neural proteins and antibodies, cytokines, agonists and antagonists.

Pathways and Genes Related to Epilepsy and Seizures

Super pathways	Top Affiliating Genes
Transmission across chemical synapses	KCNV2, KCNQ3, KCNJ9, KCNJ4, KCNJ3, KCNJ16
Oxytocin signaling pathway	KCNJ9, KCNJ4, KCNJ3, KCNJ12
GABA receptor activation	KCNJ9, KCNJ4, KCNJ3, KCNJ16, KCNJ15, KCNJ12
Potassium channels	KCNV2, KCNQ3, KCNJ9, KCNJ4, KCNJ3, KCNJ16
Cardiac conduction	SCN8A, SCN1B, SCN1A, CACNB4, ATP1A3
Sudden infant death syndrome susceptibility pathway	GABRA1, CHRNB2, CHRNA4, ATP1A3
Phase 0 - rapid depolarisation	SCN8A, SCN1B, SCN1A, CACNB4

Epilepsy In Vitro Assay

For Research Use Only. Not For Clinical Use.

Target

Gemin 2

Semaphorin 7a

WNT3A

BMAL1

UNC45

LIS1

GLI1

Gephyrin

GBA

Amyloid Beta

CDK5

CNTF

eNOS

Chromogranin B

FABP2

Rab5

GSTP1

Huntingtin

BAX

Munc13-1

CDK1

SYNPR

NF2

PGP9.5

Glucagon

Mint-1

HOMER1

NEFM

FOXO1A

FABP3

APP

Neuroligin 3