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Artikel-Nr:
(HONE25017.9025)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
25017.9025
Lokale Artikelnummer::
HONE25017.9025
Beschreibung:
Kaliumacetat
VE:
1 * 25 kg
Lieferant:
LEICA HISTOLOGY
Beschreibung:
IP ActivFlo Biopsy III-Kassetten haben das patentierte „Fluidic Flow“ Porendesign für maximalen Reagenzienaustausch. Mit einer Porengröße von 0,26 mm weisen die Kassetten ein innovatives V-förmiges Porendesign auf, das Flüssigkeit nach innen zieht und Luft nach außen drückt. Durch die abgeschrägten Kassettenwände entsteht ein Korb für kleine Gewebeproben. Diese einteiligen Kassetten mit „brechbaren“ Deckeln sind für den Leica IP C Kassettendrucker konzipiert und haben eine Druckfehlerquote von <1 %.
Artikel-Nr:
(CHMP007233.0010)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
007233.0010
Lokale Artikelnummer::
CHMP007233.0010
Beschreibung:
Terbiumtrinitrat Hydrat
VE:
1 * 10 g
Artikel-Nr:
(REST25485)
Lieferant:
Restek
Hersteller-Artikelnummer::
25485
Lokale Artikelnummer::
REST25485
Beschreibung:
Replacement parts for Thermo separation HPLC systems.
VE:
1 * 1 ST
Lieferant:
Sigma-Aldrich
Beschreibung:
Terbiumtriacetat Hydrat, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-1599R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1599R-A488
Lokale Artikelnummer::
BOSSBS-1599R-A488
Beschreibung:
Calpain, and m calpain, also known as Calpain 2, are intracellular, calcium dependent cysteine proteases. Mu calpain has a micromolar sensitivity (thus the mu) as compared to the millimolar calcium sensitivity of m calpain. Both Calpains 1 and 2 are composed of an 80 kD subunit and a 30 kD subunit. Whereas the 30 kDa subunit is shared by both enzymes, the larger catalytic subunits are different and exhibit the distinct Ca++ requirements that are suggested by their names. The calpains have papain like activity, thus the pain nomenclature. Both Calpain 1 and Calpain 2 are ubiquitously expressed, and are countered by the endogenous calpain inhibitor, calpastatin. Other calpain family members (calpain 94, ncl2, ncl3, etc) have more limited tissue distribution, and perhaps different functions. The calpain family members consist of a common small subunit (Calpain 4), and a large variable subunit. It is not clear that all calpains contain a small subunit. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV. The calpains appear to serve multiple physiological roles, and ideas concerning the functions of these enzymes are in a state of rapid flux.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1599R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1599R-CY5.5
Lokale Artikelnummer::
BOSSBS-1599R-CY5.5
Beschreibung:
Calpain, and m calpain, also known as Calpain 2, are intracellular, calcium dependent cysteine proteases. Mu calpain has a micromolar sensitivity (thus the mu) as compared to the millimolar calcium sensitivity of m calpain. Both Calpains 1 and 2 are composed of an 80 kD subunit and a 30 kD subunit. Whereas the 30 kDa subunit is shared by both enzymes, the larger catalytic subunits are different and exhibit the distinct Ca++ requirements that are suggested by their names. The calpains have papain like activity, thus the pain nomenclature. Both Calpain 1 and Calpain 2 are ubiquitously expressed, and are countered by the endogenous calpain inhibitor, calpastatin. Other calpain family members (calpain 94, ncl2, ncl3, etc) have more limited tissue distribution, and perhaps different functions. The calpain family members consist of a common small subunit (Calpain 4), and a large variable subunit. It is not clear that all calpains contain a small subunit. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV. The calpains appear to serve multiple physiological roles, and ideas concerning the functions of these enzymes are in a state of rapid flux.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3008R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R-A680
Lokale Artikelnummer::
BOSSBS-3008R-A680
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterised by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1599R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1599R-CY7
Lokale Artikelnummer::
BOSSBS-1599R-CY7
Beschreibung:
Calpain, and m calpain, also known as Calpain 2, are intracellular, calcium dependent cysteine proteases. Mu calpain has a micromolar sensitivity (thus the mu) as compared to the millimolar calcium sensitivity of m calpain. Both Calpains 1 and 2 are composed of an 80 kD subunit and a 30 kD subunit. Whereas the 30 kDa subunit is shared by both enzymes, the larger catalytic subunits are different and exhibit the distinct Ca++ requirements that are suggested by their names. The calpains have papain like activity, thus the pain nomenclature. Both Calpain 1 and Calpain 2 are ubiquitously expressed, and are countered by the endogenous calpain inhibitor, calpastatin. Other calpain family members (calpain 94, ncl2, ncl3, etc) have more limited tissue distribution, and perhaps different functions. The calpain family members consist of a common small subunit (Calpain 4), and a large variable subunit. It is not clear that all calpains contain a small subunit. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV. The calpains appear to serve multiple physiological roles, and ideas concerning the functions of these enzymes are in a state of rapid flux.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3008R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R
Lokale Artikelnummer::
BOSSBS-3008R
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3008R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R-A647
Lokale Artikelnummer::
BOSSBS-3008R-A647
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3008R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3008R-A350
Lokale Artikelnummer::
BOSSBS-3008R-A350
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
VE:
1 * 100 µl
Artikel-Nr:
(CHMP1172.0250)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
1172.0250
Lokale Artikelnummer::
CHMP1172.0250
Beschreibung:
Certrichlorid Hydrat
VE:
1 * 250 g
Lieferant:
MACHEREY-NAGEL
Beschreibung:
Bestimmung von Kalium mittels Trübungsmessung.
Artikel-Nr:
(PRSI25-255)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-255
Lokale Artikelnummer::
PRSI25-255
Beschreibung:
KCNK15 is one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. KCNK15 has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity.This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity.
VE:
1 * 50 µG
Lieferant:
Thermo Orion
Beschreibung:
Ionic strength adjustors are used for analysis with ion selective electrodes, and special reagents are used with some ion selective electrodes.
Preis auf Anfrage
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 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.
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