Gene:  KCNQ1, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair gene expression assay target

Why PrimePCR?

PrimePCR
Lookup Tool
Design and Validation of Real-Time PCR Primers-test
Pathway Curation
and Array Design Strategy
Control and Reference Assays for Real-Time PCR

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]

PrimePCR™ SYBR® Green Assay: KCNQ1, Human
potassium voltage-gated channel, KQT-like subfamily, member 1

Assay Type: SYBR® Green
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCID0007481
Info:   Same primer pair as used in probe assay qHsaCIP0026485
List Price:    $146.00
Your Price:   Log In
Quantity:  
 
Add to Custom Plate
PrimePCR™ Probe Assay: KCNQ1, Human
potassium voltage-gated channel, KQT-like subfamily, member 1

Assay Type: Probe
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCIP0026485
List Price:    $214.00
Your Price:   Log In
Quantity:  
 
Number Description Download