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BELLINGHAM++STANLEY
Artikel-Nr:
(BOSSBS-9716R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-FITC
Lokale Artikelnummer::
BOSSBS-9716R-FITC
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9716R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-CY5
Lokale Artikelnummer::
BOSSBS-9716R-CY5
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chlor-3-hydroxybenzaldehyd 98%
Artikel-Nr:
(558-0354)
Lieferant:
SGE Analytical Science
Hersteller-Artikelnummer::
0726280
Lokale Artikelnummer::
SGEA0726280
Beschreibung:
Autosampler-Spritzen für PerkinElmer AutoSystem.
VE:
1 * 10 ST
Artikel-Nr:
(APOSOR8948-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR8948-25G
Lokale Artikelnummer::
APOSOR8948-25G
Beschreibung:
6-Chloro-2H-[1,4]benzoxazine-3(4H)-one
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-11589R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11589R-CY7
Lokale Artikelnummer::
BOSSBS-11589R-CY7
Beschreibung:
The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxC5 is a 222 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Existing as multiple alternatively spliced isoforms, HoxC5 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. The gene encoding HoxC5 maps to a cluster of Hox proteins on chromosome 12 that are essential for morphogenesis. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9448R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-CY7
Lokale Artikelnummer::
BOSSBS-9448R-CY7
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6384R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6384R-CY5
Lokale Artikelnummer::
BOSSBS-6384R-CY5
Beschreibung:
C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11377R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11377R
Lokale Artikelnummer::
BOSSBS-11377R
Beschreibung:
The inositol polyphosphate 5-phosphatases selectively remove the phosphate from the 5-position of various phosphatidylinositols, which generate second messengers in response to extracellular signals. Synaptojanins are characterized by an N-terminal SAC1-like sequence, a central 5-phosphate domain, and a unique C-terminal sequence and have been shown to use phosphatidylinositol 4,5-bisphosphate as a substrate. Synaptojanins exist as two isoforms, synaptojanin 1 and 2, which differ in the C-terminal domain, and each isoform has multiple variants produced by alternative splicing. Synaptojanin 1 is expressed as two major forms: the shorter is found in brain while the longer is expressed in peripheral tissues. Eight splice variants of synaptojanin 2 have been detected, including a brain specific isoform. Synaptojanins are thought to participate in the endocytosis of synaptic vesicles and the regulation of the actin cytoskeleton.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-[4-Chloro-2-nitro-5-(trifluoromethyl)phenyl]-2,2,2-trifluoroacetamide
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl-2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate
Artikel-Nr:
(APOSOR8501-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR8501-1G
Lokale Artikelnummer::
APOSOR8501-1G
Beschreibung:
2-Chloro-4-(1H-1,2,4-triazol-1-yl)benzenecarbohydrazide
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)-5-methoxypyrimidin-4(3H)-one
Artikel-Nr:
(APOSPC210098-500MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC210098-500MG
Lokale Artikelnummer::
APOSPC210098-500MG
Beschreibung:
1-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]-3-(propan-2-yl)piperazine
VE:
1 * 500 mg
Artikel-Nr:
(APOSPC300543-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC300543-1G
Lokale Artikelnummer::
APOSPC300543-1G
Beschreibung:
1-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-sulphonyl chloride
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD00824665-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD00824665-1G
Lokale Artikelnummer::
BLDPBD00824665-1G
Beschreibung:
2-(4-Chloro-3-(trifluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 98%
VE:
1 * 1 g
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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