(3R,5S)-rel-3,5-Dimethylmorpholine+hydrochloride
Catalog Number:
(TCR0058-001G)
Supplier:
TCI America
Description:
CAS Number: 13021-40-4
MDL Number: MFCD00001649 Molecular Formula: C6H2O6 Molecular Weight: 246.26 Purity/Analysis Method: >95.0% (T) Form: Crystal Color: Black
Catalog Number:
(ABCA_AB7671-100UG)
Supplier:
ABCAM INC.
Description:
Anti-alpha 1 Sodium Potassium ATPase Mouse Monoclonal Antibody [clone: 464,6]
Catalog Number:
(10274-972)
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:
(10274-868)
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].
Catalog Number:
(76100-764)
Supplier:
Bioss
Description:
KCTD19 potassium channel tetramerization domain containing 19.
Catalog Number:
(EM1.99021.0001)
Supplier:
MilliporeSigma
Description:
30 ml buffers sachets - ideal for the calibration of pH meters.
Catalog Number:
(76681-440)
Supplier:
AMBEED, INC
Description:
(R)-1-Bromo-2-methylbutane, Purity: 98% (stabilized with potassium carbonate), CAS Number: 99032-67-4, Appearance: Liquid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 250MG
Catalog Number:
(10801-016)
Supplier:
Rockland Immunochemical
Description:
Sterile Plasma in Anticoagulant
Supplier:
Mettler Toledo
Description:
NIST-traceable standard for conductivity electrode calibration and verification.
Catalog Number:
(10101-188)
Supplier:
Prosci
Description:
KCTD6 is a domain of potassium channel.
Catalog Number:
(ABCA_AB217947-100U)
Supplier:
ABCAM INC.
Description:
Anti-alpha 1 Sodium Potassium ATPase Rabbit Polyclonal Antibody
Supplier:
AMBEED, INC
Description:
EDTA tripotassium salt ≥98%
Catalog Number:
(10101-232)
Supplier:
Prosci
Description:
KCNQ1 encodes a protein for a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in KCNQ1 are associated with hereditary long QT syndrome, Romano-Ward syndrome, Jervell and Lange-Nielsen syndrome and familial atrial fibrillation.
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