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Potassium+(2-acetylphenyl)trifluoroborate
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Potassium+(2-acetylphenyl)trifluoroborate
Supplier:
Rockland Immunochemical
Description:
Sterile Plasma in Anticoagulant
Supplier:
Rockland Immunochemical
Description:
Sterile Plasma in Anticoagulant
Supplier:
Rockland Immunochemical
Description:
Sterile Plasma in Anticoagulant
Catalog Number:
(10274-990)
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. [provided by RefSeq]
Catalog Number:
(10329-764)
Supplier:
Bioss
Description:
Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoforms USO have no channel activity by themself, but modulates channel characteristics by forming heterotetramers with other isoforms which are retained intracellularly and undergo ubiquitin-dependent degradation.
Catalog Number:
(10349-128)
Supplier:
Bioss
Description:
This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene.
Catalog Number:
(AAJ60832-AK)
Supplier:
Thermo Scientific Chemicals
Description:
250ml CAS: 127-08-2, MDL: MFCD00012458 Liquid
Supplier:
Southern Biotechnology
Description:
Gelatin Subbed Slides are subbed with a solution of 0.1% gelatin and chromium potassium sulfate.
Catalog Number:
(89323-636)
Supplier:
Genetex
Description:
Solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: WB Pkg Size: 100 ul
Supplier:
BeanTown Chemical
Description:
CAS: 7447-40-7
EC No: 231-211-8 Linear formula: KCl Form: Liquid Vapor pressure at 20 °C (68 °F): 23 hPa (17.3 mm Hg) Density at 20 °C (68 °F): 1 g/cm³ (8.345 lbs./gal) Solvent content: Water: 99.9% Solids content: 0.1%
Supplier:
Thermo Scientific Chemicals
Description:
Standard for TOC based on potassium hydrogen phthalate (KHC₈H₄O₄).
Catalog Number:
(10275-748)
Supplier:
Bioss
Description:
Potassium 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, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, members of which allow nerve cells to efficiently repolarize following an action potential. It plays an essential role in T-cell proliferation and activation. This gene appears to be intronless and it is clustered together with KCNA2 and KCNA10 genes on chromosome 1. [provided by RefSeq, Jul 2008].
Supplier:
Rockland Immunochemical
Description:
Non-Sterile Plasma in Anticoagulant
Supplier:
Rockland Immunochemical
Description:
Non-Sterile Plasma in Anticoagulant
Catalog Number:
(77439-618)
Supplier:
Bioss
Description:
Transporter which plays an important role in sodium-mediated fluid transport in different organs. Prevents severe morphological changes of the cornea caused by increased sodium chloride concentrations in the stroma. In the inner ear, is involved in transport of potassium through the fibrocyte layer to the stria vascularis and is essential for the generation of the endocochlear potential but not for regulation of potassium concentrations in the endolymph. In the kidney, is essential for urinary concentration, mediates a sodium flux into the thin descending limb of Henle loop to allow countercurrent multiplication by osmotic equilibration (By similarity). Involved in borate homeostasis. In the absence of borate, it functions as a Na(+) and OH(-)(H(+)) channel. In the presence of borate functions as an electrogenic Na(+) coupled borate cotransporter.
Supplier:
Rockland Immunochemical
Description:
Non-Sterile Plasma in Anticoagulant
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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