1-(4-Chlorophenyl)-1-methylethylamine
Artikel-Nr:
(SIAL329061-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
329061-5G
Lokale Artikelnummer::
SIAL329061-5G
Beschreibung:
2-Mercaptopyridin-N-oxid Natriumsalz, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-12127R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12127R-A350
Lokale Artikelnummer::
BOSSBS-12127R-A350
Beschreibung:
Voltage-gated sodium channels are selective ion channels that regulate the permeability of sodium ions in excitable cells. During the propagation of an action potential, sodium channels allow an influx of sodium ions, which rapidly depolarize the cell. The three glycoproteins that comprise the voltage-gated sodium channel proteins include a pore-forming Beta subunit, a noncovalently associated Beta 1 subunit and a disulfide-linked Beta 2 subunit. Na+ CP type VII Alpha (Sodium channel protein type 7 subunit alpha), also known as SCN6A, Sodium channel protein cardiac and skeletal muscle subunit alpha and putative voltage-gated sodium channel subunit alpha Nax, is a 1682 amino acid multi-pass membrane protein that belongs to the sodium channel family. Primarily expressed in uterus and heart, Na+ CP type VII Alpha may function in the regulation of salt intake behavior and central sensing of body-fluid sodium levels.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-A647
Lokale Artikelnummer::
BOSSBS-13627R-A647
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-A350
Lokale Artikelnummer::
BOSSBS-13627R-A350
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-HRP
Lokale Artikelnummer::
BOSSBS-13627R-HRP
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Lieferant:
Corning Life Science
Beschreibung:
Ampicillin ist ein Penicillin-Derivat, das die bakterielle Zellwandsynthese durch Inaktivierung der Transpeptidasen auf den inneren Oberfläche der bakteriellen Zellmembran hemmt. Ein ß-Lactam-Antibiotikum mit einer mit der Penicillinstruktur verbundenen Aminogruppen-Seitenkette, dessen Resistenz durch die Spaltung des ß-Lactam-Rings von Ampicillin durch ß-Lactamase hervorgerufen wird. Ampicillin ist wirksam gegen Gram-positive und einige Gram-negative Bakterien.
Lieferant:
Bernd Kraft
Beschreibung:
EDTA Dinatriumsalz 0.05 mol/l (0.1 N) in wässriger Lösung für die Metalltitration
Lieferant:
Bernd Kraft
Beschreibung:
EDTA Dinatriumsalz 0.1 mol/l (0.2 N) in wässriger Lösung für die Metalltitration
Lieferant:
Bernd Kraft
Beschreibung:
EDTA Dinatriumsalz 0.02 mol/l (0.04 N) in wässriger Lösung Reag. Ph. Eur.
Artikel-Nr:
(MOLE65542831-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
65542831-100G
Lokale Artikelnummer::
MOLE65542831-100G
Beschreibung:
4-Sulfobenzoesäure Monokaliumsalz
VE:
1 * 100 g
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Artikel-Nr:
(ICNA0520331125)
Lieferant:
MP Biomedicals
Hersteller-Artikelnummer::
0520331125
Lokale Artikelnummer::
ICNA0520331125
Beschreibung:
<B>Synonyms: </B>Abeson Nam; Conoco C-50; Santomerse 3; Sulphramin 85; Dodecylbenzenesulphonic acid sodium salt; Dodecylbenzene sodium sulphonate.
VE:
1 * 25 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Uranin, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-13627R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R
Lokale Artikelnummer::
BOSSBS-13627R
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10307R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10307R-A350
Lokale Artikelnummer::
BOSSBS-10307R-A350
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-10307R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10307R-A750
Lokale Artikelnummer::
BOSSBS-10307R-A750
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterised by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent's disease, a renal disorder characterised by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
VE:
1 * 100 µl
Artikel-Nr:
(SIALT5441-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
T5441-100G
Lokale Artikelnummer::
SIALT5441-100G
Beschreibung:
TAPS-Natriumsalz (3-(Tris(hydroxymethyl)methylamino)propansulfonsäure Natriumsalz), Sigma-Aldrich®
VE:
1 * 100 g
Preis auf Anfrage
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