KCNQ1 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNQ1
Target Synonym: ATFB1;ATFB3;FLJ26167;IKs producing slow voltage-gated potassium channel subunit alpha;IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1;Jervell and Lange-Nielsen syndrome 1;JLNS1;KCNA8;KCNA9;KCNQ1;KCNQ1;kidney and cardiac voltage dependend K+ channel;KQT-like 1;Kv1.9;Kv7.1;KVLQT1;long (electrocardiographic) QT syndrome;Ward-Romano syndrome 1;LQT;LQT1;Potassium channel;voltage-gated;shaker-relatd subfamily;member 9;Potassium voltage-gated channel subfamily KQT member 1;potassium voltage-gated channel;KQT-like subfamily;member 1;RWS;slow delayed rectifier channel subunit;SQT2;Voltage-gated potassium channel subunit Kv7.1;WRS
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51787
Accession:
Background: 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.
Concentration: 0.2 mg/mL
Immunogen: Recombinant protein of human KCNQ1
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:200-1:1000;IHC 1:50-1:200
Calculated MW: 75kDa
ObservedMW:
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KCNQ1 Polyclonal Antibody
KCNQ1 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNQ1
Target Synonym: ATFB1;ATFB3;FLJ26167;IKs producing slow voltage-gated potassium channel subunit alpha;IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1;Jervell and Lange-Nielsen syndrome 1;JLNS1;KCNA8;KCNA9;KCNQ1;KCNQ1;kidney and cardiac voltage dependend K+ channel;KQT-like 1;Kv1.9;Kv7.1;KVLQT1;long (electrocardiographic) QT syndrome;Ward-Romano syndrome 1;LQT;LQT1;Potassium channel;voltage-gated;shaker-relatd subfamily;member 9;Potassium voltage-gated channel subfamily KQT member 1;potassium voltage-gated channel;KQT-like subfamily;member 1;RWS;slow delayed rectifier channel subunit;SQT2;Voltage-gated potassium channel subunit Kv7.1;WRS
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51787
Accession:
Background: 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.
Concentration: 0.2 mg/mL
Immunogen: Recombinant protein of human KCNQ1
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:200-1:1000;IHC 1:50-1:200
Calculated MW: 75kDa
ObservedMW:
Original: $358.65
-70%$358.65
$107.59Product Information
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Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNQ1
Target Synonym: ATFB1;ATFB3;FLJ26167;IKs producing slow voltage-gated potassium channel subunit alpha;IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1;Jervell and Lange-Nielsen syndrome 1;JLNS1;KCNA8;KCNA9;KCNQ1;KCNQ1;kidney and cardiac voltage dependend K+ channel;KQT-like 1;Kv1.9;Kv7.1;KVLQT1;long (electrocardiographic) QT syndrome;Ward-Romano syndrome 1;LQT;LQT1;Potassium channel;voltage-gated;shaker-relatd subfamily;member 9;Potassium voltage-gated channel subfamily KQT member 1;potassium voltage-gated channel;KQT-like subfamily;member 1;RWS;slow delayed rectifier channel subunit;SQT2;Voltage-gated potassium channel subunit Kv7.1;WRS
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51787
Accession:
Background: 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.
Concentration: 0.2 mg/mL
Immunogen: Recombinant protein of human KCNQ1
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:200-1:1000;IHC 1:50-1:200
Calculated MW: 75kDa
ObservedMW:
