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Terbium(III)chlorid
Artikel-Nr:
(BOSSBS-6662R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6662R-CY5.5
Lokale Artikelnummer::
BOSSBS-6662R-CY5.5
Beschreibung:
This gene encodes a member of the tyrosine kinase and, more specifically, the Janus kinases (JAKs) protein families. This protein associates with the cytoplasmic domain of type I and type II cytokine receptors and promulgate cytokine signals by phosphorylating receptor subunits. It is also component of both the type I and type III interferon signaling pathways. As such, it may play a role in anti-viral immunity. A mutation in this gene has been associated with hyperimmunoglobulin E syndrome (HIES) - a primary immunodeficiency characterized by elevated serum immunoglobulin E. [provided by RefSeq].
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-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-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:
(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-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-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
Lieferant:
Alfa Aesar
Beschreibung:
Antimon(V)chlorid, ultra trocken ≥99,999% (Metall-Basis)
Artikel-Nr:
(436080500.)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
436080500
Lokale Artikelnummer::
ACRO436080500
Beschreibung:
Methylzinc chloride 2 M in THF, AcroSeal®
VE:
1 * 50 mL
Artikel-Nr:
(APOSPC302763-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC302763-1G
Lokale Artikelnummer::
APOSPC302763-1G
Beschreibung:
6-Chloro-2,3-difluorobenzoyl chloride 98%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1,3-Benzothiazole-6-sulphonyl chloride 95%
Artikel-Nr:
(BOSSBS-12500R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12500R-CY3
Lokale Artikelnummer::
BOSSBS-12500R-CY3
Beschreibung:
The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-V (apolipoprotein L-V), also known as APOL5, is a 433 amino acid protein that localizes to the cytoplasm and belongs to the apolipoprotein L family. Expressed in a variety of tissues including testis, stomach, uterus and skeletal muscle, apoL-V is thought to affect the movement of lipids in the cytoplasm and may allow the binding of lipids to organelles. Like other members of the apolipoprotein L family, apoL-V is thought to be involved in the development of schizophrenia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13058R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13058R-HRP
Lokale Artikelnummer::
BOSSBS-13058R-HRP
Beschreibung:
Eukaryotic elongation factor 2 kinase (EEF2k) previously known as Ca2+/calmodulin dependent protein kinase III, is an abundant cytoplasmic protein highly specific for elongation factor 2 (eEf2). Phosphorylation of eEF2 by eEF2 kinase on specific threonine residues results in the inactivation of eEF-2 and in termination of mRNA translation. The activity of eEF2 kinase is not only dependent upon Ca2+ ions, calmodulin (CaM) and insulin, but is also regulated both negatively and positively via phosphorylation by different protein kinases (AMPK, S6K1, p90 RSK). There is also evidence that eEF-2 phosphorylation is involved in the regulation of cell cycle progression, cellular differentiation, oogensis and malignant tumors.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11636R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11636R
Lokale Artikelnummer::
BOSSBS-11636R
Beschreibung:
Contactins mediate cell surface interactions during nervous system development. Participates in oligodendrocytes generation by acting as a ligand of NOTCH1. Its association with NOTCH1 promotes NOTCH1 activation through the released notch intracellular domain (NICD) and subsequent translocation to the nucleus. Involved in motor coordination. Tissue specificity: Expressed in nervous system. Highly expressed in cerebellum. Expressed at intermediate level in thalamus, subthalamic nucleus. Weakly expressed in corpus callosum, caudate nucleus and spinal cord. Similarity: Belongs to the immunoglobulin superfamily. Contactin family. Contains 4 fibronectin type-III domains. Contains 6 Ig-like C2-type (immunoglobulin-like) domains.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chloro-3-(trifluoromethyl)benzyl chloride 98%
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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