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|NCBI Gene ID:||3784|
|Official Full Name:||potassium voltage-gated channel subfamily Q member 1|
|Summary:|| This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011].|
There is no existing raPOOL for your gene, hence a custom raPOOL set up service is required. Please add this to cart and proceed to choose the raPOOL scale required where 2, 5 or 10 nmol is sufficient for 20, 50 or 100 reactions with the recommended use of 100 pmol raPOOL per reaction.
Custom raPOOL Set Up Service
One-time raPOOL set up fee for a new gene.
Price: € 529,00
Includes design of new probes against target RNA. Charged on top of raPOOL 2, 5 or 10 price.
Charged once only, subsequent order of raPOOL follows raPOOL-2, 5 or 10 pricing.
Price: € 1.155,00
Amount provided: 10 nmol. Sufficient for 100 reactions.
Price: € 325,00
Amount provided: 2 nmol. Sufficient for 20 rxns.
5 nmol raPOOL
Price: € 675,00
Amount provided: 5 nmol. Sufficient for 50 reactions.