6-(Piperidin-1-yl)pyridine-2-carboxaldehyde
Lieferant:
Alfa Aesar
Beschreibung:
Arsenazo III
Artikel-Nr:
(ABCRAB101280.0025)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB101280.0025
Lokale Artikelnummer::
ABCRAB101280.0025
Beschreibung:
Ruthenium(III)chlorid Hydrat
VE:
1 * 25 g
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Lieferant:
CHEMPUR
Beschreibung:
Vanadium(III)fluorid
Artikel-Nr:
(BOSSBS-9045R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9045R-CY5.5
Lokale Artikelnummer::
BOSSBS-9045R-CY5.5
Beschreibung:
Receptor-activated non-selective cation channel involved in detection of sensations such as coolness, by being activated by cold temperature below 25 degrees Celsius. Activated by icilin, eucalyptol, menthol, cold and modulation of intracellular pH. Involved in menthol sensation. Permeable for monovalent cations sodium, potassium, and cesium and divalent cation calcium. Temperature sensing is tightly linked to voltage-dependent gating. Activated upon depolarization, changes in temperature resulting in graded shifts of its voltage-dependent activation curves. The chemical agonists menthol functions as a gating modifier, shifting activation curves towards physiological membrane potentials. Temperature sensitivity arises from a tenfold difference in the activation energies associated with voltage-dependent opening and closing.
VE:
1 * 100 µl
Artikel-Nr:
(ABCRAV17399.0025)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AV17399.0025
Lokale Artikelnummer::
ABCRAV17399.0025
Beschreibung:
Thallium(III)nitrat
VE:
1 * 25 g
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Artikel-Nr:
(BOSSBS-10448R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10448R-HRP
Lokale Artikelnummer::
BOSSBS-10448R-HRP
Beschreibung:
This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8498R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8498R-HRP
Lokale Artikelnummer::
BOSSBS-8498R-HRP
Beschreibung:
REG1 beta is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. REG1 beta highly similar to the REG1 alpha protein. The related REG1 alpha protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic lithogenesis. Reg family members REG1 alpha, REGL, PAP and this gene are tandomly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
Lanthan(III)fluorid
Artikel-Nr:
(BOSSBS-7974R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-HRP
Lokale Artikelnummer::
BOSSBS-7974R-HRP
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. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7974R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-A647
Lokale Artikelnummer::
BOSSBS-7974R-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. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7974R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-A350
Lokale Artikelnummer::
BOSSBS-7974R-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. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3953R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3953R-A647
Lokale Artikelnummer::
BOSSBS-3953R-A647
Beschreibung:
Cytochrome c oxidase subunit I (COI or MTCO1) is one of three mitochondrial DNA (mtDNA) encoded subunits (MTCO1, MTCO2, MTCO3) of respiratory Complex IV. Complex IV is located within the mitochondrial inner membrane and is the third and final enzyme of the electron transport chain of mitochondrial oxidative phosphorylation. Complex IV is composed of 13 polypeptides. Subunits I, II, and III (MTCO1, MTCO2, MTCO3) are encoded by mtDNA while subunits IV, Va, Vb, VIa, VIb, VIc, VIIa, VIIb, VIIc, and VIII are nuclear encoded. Mammalian MTCO1 has 12 membrane-spanning alpha-helices (I to XII).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7974R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-A680
Lokale Artikelnummer::
BOSSBS-7974R-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. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterised by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3953R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3953R-FITC
Lokale Artikelnummer::
BOSSBS-3953R-FITC
Beschreibung:
Cytochrome c oxidase subunit I (COI or MTCO1) is one of three mitochondrial DNA (mtDNA) encoded subunits (MTCO1, MTCO2, MTCO3) of respiratory Complex IV. Complex IV is located within the mitochondrial inner membrane and is the third and final enzyme of the electron transport chain of mitochondrial oxidative phosphorylation. Complex IV is composed of 13 polypeptides. Subunits I, II, and III (MTCO1, MTCO2, MTCO3) are encoded by mtDNA while subunits IV, Va, Vb, VIa, VIb, VIc, VIIa, VIIb, VIIc, and VIII are nuclear encoded. Mammalian MTCO1 has 12 membrane-spanning alpha-helices (I to XII).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7974R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-FITC
Lokale Artikelnummer::
BOSSBS-7974R-FITC
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. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(CHMP004156.0005)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
004156.0005
Lokale Artikelnummer::
CHMP004156.0005
Beschreibung:
Tetrachlorgold(III)säure (40 - 44% Au) in wässriger Lösung
VE:
1 * 5 g
Preis auf Anfrage
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