Suche >
EDTA+disodium+salt+solution+with+zinc+complex+added+(solution+B)
Drucken
Sie suchten nach:
78 811 results were found
EDTA+disodium+salt+solution+with+zinc+complex+added+(solution+B)
Artikel-Nr:
(BOSSBS-10307R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10307R-CY5
Lokale Artikelnummer::
BOSSBS-10307R-CY5
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10307R-CY3
Lokale Artikelnummer::
BOSSBS-10307R-CY3
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:
(PRSI90-327)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
90-327
Lokale Artikelnummer::
PRSI90-327
Beschreibung:
Zinc-alpha-2-glycoprotein (ZAG), first identified in the 1960s, derives its name from its precipitation from human plasma upon the addition of zinc salts. ZAG has since been found in secretory epithelial cells and in a range of body fluids. ZAG is identical to a lipid mobilizing factor isolated from the urine of patients with cancer cachexia and stimulates lipolysis in in vitro and in vivo experiments. Due to its expression in, and secretion from adipocytes, ZAG is considered an adipokine. Recently the clinical significance of ZAG has been clarified. ZAG expression in adipocytes is inversely related to fat mass, thus it is intimately involved in the maintenance of body weight in mice and humans. Epidemiological studies have uncovered an association between ZAG and plasma cholesterol. The non-synonymous single nucleotide polymorphism rs4215 in ZAG is associated with plasma cholesterol and obesity. Structurally ZAG possesses a class I major histocompatibility complex (MHC) protein fold. It is distinct from other members of this protein family in that it is soluble, rather than being anchored to plasma membranes, and it associates with prolactin inducible protein rather than beta2-microglobulin. Similar to peptide antigen-presenting class I MHC molecules, ZAG possesses an open apical groove between its alpha1 and alpha2 domain helices.
VE:
1 * 50 µG
Lieferant:
Thermo Scientific
Beschreibung:
PIPES Dinatriumsalz 99%
Artikel-Nr:
(BOSSBS-10307R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10307R-HRP
Lokale Artikelnummer::
BOSSBS-10307R-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. 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Substrate for Alkaline phosphatase.
Lieferant:
Merck
Beschreibung:
Natriummetabisulfit, EMSURE® ACS, Reag. Ph. Eur. zur Analyse, Supelco®
Lieferant:
Bernd Kraft
Beschreibung:
Natriumacetat 20% aqueous solution, extra_pure
Artikel-Nr:
(F7258-25G)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
F7258-25G
Lokale Artikelnummer::
SIAMF7258-25G
Beschreibung:
Echtgrün FCF, Sigma-Aldrich®
VE:
1 * 25 g
Lieferant:
Alfa Aesar
Beschreibung:
Bathocuproinsulfonat Dinatriumsalz Hydrat ≥97%
Artikel-Nr:
(2386-20)
Lieferant:
MACRON AVANTOR BRAND
Lokale Artikelnummer::
MACR2386-20
Beschreibung:
di-Natrium-L(+)-tartrat Dihydrat 99,0-101,0%, körnig, AR® ACS, Macron Fine Chemicals™
VE:
1 * 12 kg
Artikel-Nr:
(APOSBID2033-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BID2033-100MG
Lokale Artikelnummer::
APOSBID2033-100MG
Beschreibung:
2'-Desoxyadenosin-5'-triphosphat Dinatriumsalz (dATP Dinatriumsalz) 97+%
VE:
1 * 100 mg
Artikel-Nr:
(HEID501-61029-00)
Lieferant:
Heidolph Instruments GmbH & Co.KG
Hersteller-Artikelnummer::
501-61029-00
Lokale Artikelnummer::
HEID501-61029-00
Beschreibung:
In order to provide the perfect end-to-end solution for powerful stirring and the simplest operation in the laboratory, we have added packages to the Hei-TORQUE product group.Each package contains a telescopic stand and a suitable clamp for easy use on lab tables.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-13627R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-A750
Lokale Artikelnummer::
BOSSBS-13627R-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. 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:
Alfa Aesar
Beschreibung:
Creatinphosphat Dinatriumsalz Tetrahydrat ≥98%
Preis auf Anfrage
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
