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Artikel-Nr:
(BOSSBS-12207R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12207R-A350
Lokale Artikelnummer::
BOSSBS-12207R-A350
Beschreibung:
UTF1 is a 341 amino acid protein that localizes to the nucleus and is subject to post-translational phosphorylation. Associating with the TFIID complex via an interaction with the TATA box binding protein (TFIID), UTF1 binds to the N-terminal region of ATF-2 and, via this binding, acts as a transcriptional coactivator of ATF-2, thereby enhancing transcriptional activity. Human UTF1 shares 64% homology with its mouse counterpart, suggesting a similar role between species. The gene encoding UTF1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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-9887R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9887R-A750
Lokale Artikelnummer::
BOSSBS-9887R-A750
Beschreibung:
p22HBP, also known as HEBP1 (heme binding protein 1), HBP or HEBP, is a 189 amino acid intracellular tetrapyrrole-binding protein that assists in prevention of cellular toxicity by removing free porphyrinogens from the cell. Existing as a monomer, p22HBP localizes to cytoplasm and contains a 21 amino acid chemoattractant within its N-terminus that functions as a natural ligand for FPR3. p22HBP is a member of the HEBP family and binds N-methylprotoporphyrin and metalloporphyrins with similar affinity to porphyrinogens. The gene encoding p22HBP maps to human chromosome 12, which 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-12207R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12207R-CY3
Lokale Artikelnummer::
BOSSBS-12207R-CY3
Beschreibung:
UTF1 is a 341 amino acid protein that localizes to the nucleus and is subject to post-translational phosphorylation. Associating with the TFIID complex via an interaction with the TATA box binding protein (TFIID), UTF1 binds to the N-terminal region of ATF-2 and, via this binding, acts as a transcriptional coactivator of ATF-2, thereby enhancing transcriptional activity. Human UTF1 shares 64% homology with its mouse counterpart, suggesting a similar role between species. The gene encoding UTF1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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-12207R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12207R-A680
Lokale Artikelnummer::
BOSSBS-12207R-A680
Beschreibung:
UTF1 is a 341 amino acid protein that localizes to the nucleus and is subject to post-translational phosphorylation. Associating with the TFIID complex via an interaction with the TATA box binding protein (TFIID), UTF1 binds to the N-terminal region of ATF-2 and, via this binding, acts as a transcriptional coactivator of ATF-2, thereby enhancing transcriptional activity. Human UTF1 shares 64% homology with its mouse counterpart, suggesting a similar role between species. The gene encoding UTF1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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-8215R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8215R-CY5
Lokale Artikelnummer::
BOSSBS-8215R-CY5
Beschreibung:
FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes 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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9743R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9743R-CY5.5
Lokale Artikelnummer::
BOSSBS-9743R-CY5.5
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 maps to human chromosome 12, which 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:
(FLUO011119-25G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
011119-25G
Lokale Artikelnummer::
FLUO011119-25G
Beschreibung:
4-Chlor-3-nitrozimtsäure
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
D(-)-Fructose, Sigma-Aldrich®
Lieferant:
Sigma-Aldrich
Beschreibung:
DL-Apfelsäure, Sigma-Aldrich®
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-(Butylcarbamoyl)phenylboronsäure
Lieferant:
COMBI-BLOCKS
Beschreibung:
(1H-Pyrazol-1-yl)essigsäure
Lieferant:
U-Power
Beschreibung:
100% metal-free safety shoes made from breathable and water repellent New Safety Dry material and a slip and abrasion resistant U.Grip68 PUR sole.
Lieferant:
COMBI-BLOCKS
Beschreibung:
Methyl-8-brom-5-fluor-4-hydroxychinolin-2-carboxylat
Artikel-Nr:
(SIAL754730-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
754730-1G
Lokale Artikelnummer::
SIAL754730-1G
Beschreibung:
Tris(2,2′-bipyridine)ruthenium(II) hexafluorophosphate is a high efficiency triplet emitter for OLED/sensor research.
VE:
1 * 1 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Testbenzin, 150…200 °C, Sigma-Aldrich®
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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