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Potassium+(tert-butoxymethyl)trifluoroborate
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Potassium+(tert-butoxymethyl)trifluoroborate
Catalog Number:
(10274-976)
Supplier:
Bioss
Description:
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. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel and its activity is modulated by some other family members. [provided by RefSeq].
Catalog Number:
(76483-188)
Supplier:
AAT BIOQUEST INC
Description:
Quin-2 binds calcium tightly and resembles calcium chelator EGTA in ability to bind calcium much more tightly than magnesium.
Catalog Number:
(10425-632)
Supplier:
Bioss
Description:
Protease. May regulate the surface expression of some potassium channels by retaining them in the endoplasmic reticulum (By similarity).
Catalog Number:
(10425-628)
Supplier:
Bioss
Description:
Protease. May regulate the surface expression of some potassium channels by retaining them in the endoplasmic reticulum (By similarity).
Catalog Number:
(10106-754)
Supplier:
Prosci
Description:
The functions of Voltage-gated potassium (Kv) channels include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. KCNAB2 is a member of the potassium channel, voltage-gated, shaker-related subfamily. This member is one of the beta subunits, which are auxiliary proteins associating with functional Kv-alpha subunits.
Catalog Number:
(EM1.07205.0105)
Supplier:
MilliporeSigma
Description:
Potassium Hydrogen Phosphate/Di-Sodium Hydrogen Phosphate, Directly Traceable To Primary Srm From NIST/Ptb
Catalog Number:
(76081-382)
Supplier:
Bioss
Description:
pH-dependent, voltage-insensitive, background potassium channel protein.
Catalog Number:
(76359-830)
Supplier:
Mettler Toledo
Description:
Mettler-Toledo offers electrolytes for every application. Fill-up your electrode with correct and fresh electrolyte for a precise measurement.
Catalog Number:
(10164-174)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to Sodium/Potassium ATPase alpha 3
Catalog Number:
(10454-156)
Supplier:
Bioss
Description:
Probably important in cardiac repolarization. Associates with KCNE1 (MinK) to form the I(Ks) cardiac potassium current. Elicits a rapidly activating, potassium-selective outward current. Muscarinic agonist oxotremorine-M strongly suppresses KCNQ1/KCNE1 current in CHO cells in which cloned KCNQ1/KCNE1 channels were coexpressed with M1 muscarinic receptors. May associate also with KCNE3 (MiRP2) to form the potassium channel that is important for cyclic AMP-stimulated intestinal secretion of chloride ions, which is reduced in cystic fibrosis and pathologically stimulated in cholera and other forms of secretory diarrhea.
Catalog Number:
(10101-796)
Supplier:
Prosci
Description:
KCNN2 is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. This protein is a member of the KCNN family of potassium channel genes. Two transcript variants encoding different isoforms have been found for KCNN2.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. KCNN2 is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP.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. Two transcript variants encoding different isoforms have been found for this gene.
Supplier:
AMBEED, INC
Description:
Potassium [2,2'-biquinoline]-4,4'-dicarboxylate, Purity: 98% (Loss on drying less than or equal to 10%), CAS Number: 63451-34-3, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 100g
Catalog Number:
(82021-512)
Supplier:
G-Biosciences
Description:
Molecular biology universal kit, contains 25 ml each of ammonium acetate, calcium chloride, EDTA, lithium acetate, magnesium chloride, potassium acetate, potassium chloride, SDS, sodium chloride, TE, Tris pH 7,0 and Tris pH 8,0
Catalog Number:
(BJ60131-500ML)
Supplier:
Honeywell Research Chemicals
Description:
Potassium chloride, CAS Number: 7447-40-7, Grade: Analytical Reagent, Molar Mass: 74.55 g/mol, conductivity 111.8 mS/cm at 25 deg C, conductance standard, Density (D 20/4) 1.043 - 1.045, Conductivity 25 deg C 110700 - 112900 uS/cm, Size: 500ML
Catalog Number:
(76098-950)
Supplier:
Bioss
Description:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. .
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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