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6-Fluoro-4-chromanone
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6-Fluoro-4-chromanone
Lieferant:
BURKLE
Beschreibung:
The vacuum hand pump can be operated with one hand to create a vacuum or pressure, independent of power supply.
Artikel-Nr:
(BOSSBS-1890R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1890R-CY5.5
Lokale Artikelnummer::
BOSSBS-1890R-CY5.5
Beschreibung:
Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. It is heterogeneously expressed in the brain, and mutations in this gene have been linked to several seizure disorders. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD18516-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD18516-100MG
Lokale Artikelnummer::
BLDPBD18516-100MG
Beschreibung:
3-Hydroxy-2-pyrrolidinone 97%
VE:
1 * 100 mg
Lieferant:
Thermo Scientific
Beschreibung:
(±)-γ-Hexalacton 98%
Artikel-Nr:
(BOSSBS-8409R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-HRP
Lokale Artikelnummer::
BOSSBS-8409R-HRP
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9380R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-A647
Lokale Artikelnummer::
BOSSBS-9380R-A647
Beschreibung:
Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Benzyl-4-oxo-1-piperidinecarboxylate 97%
Artikel-Nr:
(BOSSBS-11861R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11861R-A680
Lokale Artikelnummer::
BOSSBS-11861R-A680
Beschreibung:
HAP1 (huntingtin-associated protein 1) binds to huntingtin. Huntingtin is a protein that contains a polyglutamine region and when the number of glutamine repeats exceeds 35, the gene encodes a version of huntingtin that leads to Huntington’s disease (HD). The ability of HAP1 to bind to huntingtin is enhanced by an expanded polyglutamine repeat region. HAP1 shows neuronal localisation and moves with huntingtin in nerve fibers. HAP1 is primarily expressed in brain tissue, with greater expression in the olfactory bulb and brain stem. Mouse HAP1 is localised to membrane-bound organelles including large endosomes, tubulovesicular structures and budding vesicles in neurons. Duo, also designated huntingtin-associated protein interacting protein or HAPIP, binds Huntingtin-associated protein 1 (HAP1) and may have a role in vesicle trafficking and cytoskeletal function.
VE:
1 * 100 µl
Artikel-Nr:
(ACRO466832500)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
466832500
Lokale Artikelnummer::
ACRO466832500
Beschreibung:
Gentiopicroside
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
ω-Brom-2-hydroxyacetophenon
Lieferant:
Alfa Aesar
Beschreibung:
Ethylmethylketon ≥97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Methyl-5-(trifluoromethyl)-1H-pyrazol-3-ol 97%
Artikel-Nr:
(BOSSBS-11841R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11841R-HRP
Lokale Artikelnummer::
BOSSBS-11841R-HRP
Beschreibung:
TOCA-1 is a 605 amino acid protein that localizes to the cytoplasm and the cytoskeleton, as well as to cytoplasmic vesicles and the cell membrane, and contains one FCH domain, one REM repeat and one SH3 domain. Existing as multiple alternatively spliced isoforms, TOCA-1 interacts with CDC42 and is required for the coordination of membrane tubulation with Actin cytoskeletal reorganization during endocytosis. Additionally, TOCA-1 is involved in membrane invagination, tubule formation and Actin polymerization. The gene encoding TOCA-1 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome.
VE:
1 * 100 µl
Lieferant:
Bohlender
Beschreibung:
PP screw cap, blue and PTFE body.
Artikel-Nr:
(BOSSBS-9380R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-A750
Lokale Artikelnummer::
BOSSBS-9380R-A750
Beschreibung:
Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterised by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
VE:
1 * 100 µl
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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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