抗体

KCNH6 rabbit Polyclonal Antibody

KCNH6抗体
KCNH6抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily H member 6(KCNH6) Homo sapiens Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013],

KCNK2 rabbit Polyclonal Antibody

KCNK2抗体
KCNK2抗体应用:WB 1:500-2000This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

KCNK5 rabbit Polyclonal Antibody

KCNK5抗体
KCNK5抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium two pore domain channel subfamily K member 5(KCNK5) Homo sapiens This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The message for this gene is mainly expressed in the cortical distal tubules and collecting ducts of the kidney. The protein is highly sensitive to external pH and this, in combination with its expression pattern, suggests it may play an important role in renal potassium transport. [provided by RefSeq, Jul 2008],

KCNKG rabbit Polyclonal Antibody

KCNKG抗体
KCNKG抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium two pore domain channel subfamily K member 16(KCNK16) Homo sapiens The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is expressed predominantly in the pancreas and is activated at alkaline pH. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008],

KCNN1 rabbit Polyclonal Antibody

KCNN1抗体
KCNN1抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium calcium-activated channel subfamily N member 1(KCNN1) Homo sapiens Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. This gene is a member of the KCNN family of potassium channel genes. [provided by RefSeq, Jul 2008],

KCNQ1 rabbit Polyclonal Antibody

KCNQ1抗体
KCNQ1抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel subfamily Q member 1(KCNQ1) Homo sapiens 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,

KCNS1 rabbit Polyclonal Antibody

KCNS1抗体
KCNS1抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel modifier subfamily S member 1(KCNS1) Homo sapiens Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the potassium channel family. [provided by RefSeq, Jul 2008],

KCNS3 rabbit Polyclonal Antibody

KCNS3抗体
KCNS3抗体应用:WB 1:500-2000 ELISA 1:5000-20000potassium voltage-gated channel modifier subfamily S member 3(KCNS3) Homo sapiens Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the potassium channel family. Alternatively spliced transcript variants encoding the same protein have been

KCNT2 rabbit Polyclonal Antibody

KCNT2抗体
KCNT2抗体应用:WB 1:500-2000

KDIS rabbit Polyclonal Antibody

v抗体
KDIS抗体应用:WB 1:500-2000
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