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Anti-KCNQ3 Antibody (CAB20593)

SKU:
CAB20593
Product Type:
Antibody
Antibody Type:
Polyclonal Antibody
Reactivity:
Human
Host Species:
Rabbit
Isotype:
IgG
Synonyms:
EBN2
BFNC2
KV7.3
€359
Frequently bought together:

Description

Product Name:KCNQ3 Rabbit pAb
Product Code:CAB20593
Size:50uL, 100uL
Synonyms:EBN2, BFNC2, KV7.3
Applications:WB
Reactivity:Human
Host Species:Rabbit
Immunogen:A synthetic peptide corresponding to a sequence within amino acids 400-500 of human KCNQ3 (NP_001191753.1).
Applications:WB
Recommended Dilutions:WB 1:500 - 1:2000
Reactivity:Human
Immunogen:A synthetic peptide corresponding to a sequence within amino acids 400-500 of human KCNQ3 (NP_001191753.1).
Purification Method:Affinity purification
Storage:Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:IgG
Sequence:Email for sequence
Gene ID:3786
Uniprot:O43525
Calculated MW:96kDa
Observed MW:Refer to figures
UniProt Protein Function:Kv7.3: Probably important in the regulation of neuronal excitability. Associates with KCNQ2 or KCNQ5 to form a potassium channel with essentially identical properties to the channel underlying the native M-current, a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons as well as the responsiveness to synaptic inputs. Defects in KCNQ3 are the cause of benign familial neonatal seizures type 2 (BFNS2). A disorder characterized by clusters of seizures occurring in the first days of life. Most patients have spontaneous remission by 12 months of age and show normal psychomotor development. The disorder is distinguished from benign familial infantile seizures by an earlier age at onset. Belongs to the potassium channel family. KQT (TC 1.A.1.15) subfamily. Kv7.3/KCNQ3 sub-subfamily. Protein type: Membrane protein, integral; Membrane protein, multi-pass; Channel, potassium Chromosomal Location of Human Ortholog: 8q24 Cellular Component: plasma membrane Molecular Function: delayed rectifier potassium channel activity; potassium channel activity; voltage-gated potassium channel activity Biological Process: potassium ion transport; synaptic transmission Disease: Seizures, Benign Familial Neonatal, 2
UniProt Protein Details:
NCBI Summary:This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]
UniProt Code:O43525
NCBI GenInfo Identifier:5921785
NCBI Gene ID:3786
NCBI Accession:O43525.2
UniProt Secondary Accession:O43525,A2VCT8, B4DJY4, E7EQ89
UniProt Related Accession:O43525
Molecular Weight:93,599 Da
NCBI Full Name:Potassium voltage-gated channel subfamily KQT member 3
NCBI Synonym Full Names:potassium voltage-gated channel subfamily Q member 3
NCBI Official Symbol:KCNQ3  
NCBI Official Synonym Symbols:EBN2; BFNC2; KV7.3  
NCBI Protein Information:potassium voltage-gated channel subfamily KQT member 3
UniProt Protein Name:Potassium voltage-gated channel subfamily KQT member 3
UniProt Synonym Protein Names:KQT-like 3; Potassium channel subunit alpha KvLQT3; Voltage-gated potassium channel subunit Kv7.3
Protein Family:Potassium voltage-gated channel subfamily
UniProt Gene Name:KCNQ3  
UniProt Entry Name:KCNQ3_HUMAN

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