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1-(5-Methyl-2-furyl)methanamin
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1-(5-Methyl-2-furyl)methanamin
Lieferant:
ENTEGRIS
Beschreibung:
Conical pocket holds one wafer face down contacting only the edge of the wafer.
Lieferant:
Alfa Aesar
Beschreibung:
2-Bromo-1-(o-tolyl)ethanone 98%
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:
(BOSSBS-6110R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6110R
Lokale Artikelnummer::
BOSSBS-6110R
Beschreibung:
SPARC (secreted protein acidic and rich in cysteine) is a phosphorylated, acidic, glycine-rich glycoprotein that is secreted by endothelial cells and is present in large amounts in the parietal endoderm of mouse embryos and in human placenta. SPARC-like protein 1 (SPARCL1), also known as high endothelial venule protein (Hevin) or MAST9, is a 664 amino acid member of the SPARC family of proteins. Highly expressed in lymph node, heart, lung, brain, skeletal muscle, ovary, colon and small intestine, SPARCL1 is a secreted protein that contains one EF-hand domain, one follistatin-like domain and one Kazal-like domain. SPARCL1 is implicated to play a role in neuronal remodeling and tumor suppression. The gene encoding SPARCL1 maps to chromosome 4q22.1.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13147R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13147R-CY3
Lokale Artikelnummer::
BOSSBS-13147R-CY3
Beschreibung:
FNBP1 is a 617 amino acid protein that localizes to a variety of locations within the cell, including the cytoplasm, cytoskeleton, lysosome and the cell cortex, and contains one FCH domain, one REM repeat and one SH3 domain. Expressed at high levels in respiratory, reproductive and urinary systems, as well as in brown adipose tissue and epithelial cells of the gastrointestinal tract, FNBP1 interacts with Rho 7 and links the Actin cytoskeleton with Rho 7 signaling, playing a crucial role in membrane tubulation and cytoskeletal reorganization during endocytosis. Additionally, FNBP1, which exists as four alternatively spliced isoforms, enhances Actin polymerization and promotes membrane invagination and the formation of tubules. Chromosomal aberrations in the FNBP1 gene are associated with acute leukemias, suggesting a role for defective FNBP1 in carcinogenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13147R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13147R
Lokale Artikelnummer::
BOSSBS-13147R
Beschreibung:
FNBP1 is a 617 amino acid protein that localizes to a variety of locations within the cell, including the cytoplasm, cytoskeleton, lysosome and the cell cortex, and contains one FCH domain, one REM repeat and one SH3 domain. Expressed at high levels in respiratory, reproductive and urinary systems, as well as in brown adipose tissue and epithelial cells of the gastrointestinal tract, FNBP1 interacts with Rho 7 and links the Actin cytoskeleton with Rho 7 signaling, playing a crucial role in membrane tubulation and cytoskeletal reorganization during endocytosis. Additionally, FNBP1, which exists as four alternatively spliced isoforms, enhances Actin polymerization and promotes membrane invagination and the formation of tubules. Chromosomal aberrations in the FNBP1 gene are associated with acute leukemias, suggesting a role for defective FNBP1 in carcinogenesis.
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:
(±)-γ-Hexalacton 98%
Lieferant:
Thermo Scientific
Beschreibung:
1-Ethyl-2-pyrrolidon 98%
Lieferant:
Thermo Scientific
Beschreibung:
6-Methoxy-1-indanon 98%
Artikel-Nr:
(APOSOR926886-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR926886-1G
Lokale Artikelnummer::
APOSOR926886-1G
Beschreibung:
6,7-Dihydro-5h-cyclopenta[c]pyridazin-3-ol 95%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
6-Methyl-2-thiouracil ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,5-Difluoro-2-hydroxyphenacyl bromide 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
ω-Brom-2-hydroxyacetophenon
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2'-Deoxyguanosine hydrate
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
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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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