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1,6-Dibromo-2,5-dioxaperfluorohexane


144 991  results were found

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Artikel-Nr: (METR6.2743.077)

Lieferant:  METROHM
Hersteller-Artikelnummer:: 6.2743.077
Lokale Artikelnummer:: METR6.2743.077
Beschreibung:   Perforated stopper, PP, for 2,5 and 11 ml sample tubes
VE:  1 * 200 ST
Lieferant:  Bernd Kraft
Beschreibung:   A complete range of certified control standards with values ranging from 1,3 to 500 000 µS/cm to meet all the requirements for electrochemical analysis.
Lieferant:  Hettich
Beschreibung:   Adapter für 2× 25-ml-Röhrchen, Ø 26×78 mm, Tisch-Zentrifuge
Artikel-Nr: (BOSSBS-1056R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-1056R-CY5.5
Lokale Artikelnummer:: BOSSBS-1056R-CY5.5
Beschreibung:   G-protein coupled receptor for 5-hydroxytryptamine (serotonin). Also functions as a receptor for various drugs and psychoactive substances, including mescaline, psilocybin, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI) and lysergic acid diethylamide (LSD). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Beta-arrestin family members inhibit signaling via G proteins and mediate activation of alternative signaling pathways. Signaling activates phospholipase C and a phosphatidylinositol-calcium second messenger system that modulates the activity of phosphatidylinositol 3-kinase and promotes the release of Ca(2+) ions from intracellular stores. Affects neural activity, perception, cognition and mood. Plays a role in the regulation of behavior, including responses to anxiogenic situations and psychoactive substances. Plays a role in intestinal smooth muscle contraction, and may play a role in arterial vasoconstriction.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8641R-HRP
Lokale Artikelnummer:: BOSSBS-8641R-HRP
Beschreibung:   Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZDHHC1 (zinc finger, DHHC-type containing 1), also known as ZNF377 (zinc finger protein 377) or C16orf1, is a 485 amino acid multi-pass membrane protein that contains one DHHC-type zinc finger. Expressed in fetal heart, lung and kidney and also present in adult lung and pancreas, ZDHHC1 functions as a palmitoyltransferase that catalyzes the conversion of palmitoyl-CoA and protein-cysteine to S-palmitoyl protein and CoA. Like ZDHHC1, ZDHHC5, ZDHHC6, ZDHHC7 and ZDHHC18 each contain one DHHC-type zinc finger through which they convey palmitoyltransferase activity against a broad range of substrates, including H-Ras, SNAP 25 and GABAA R proteins.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-6578R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6578R
Lokale Artikelnummer:: BOSSBS-6578R
Beschreibung:   The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD14 (sterile alpha motif domain-containing protein 14) is a 417 amino acid protein encoded by the SAMD14 gene which maps to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12088R-A488
Lokale Artikelnummer:: BOSSBS-12088R-A488
Beschreibung:   Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZDHHC1 (zinc finger, DHHC-type containing 1), also known as ZNF377 (zinc finger protein 377) or C16orf1, is a 485 amino acid multi-pass membrane protein that contains one DHHC-type zinc finger. Expressed in fetal heart, lung and kidney and also present in adult lung and pancreas, ZDHHC1 functions as a palmitoyltransferase that catalyzes the conversion of palmitoyl-CoA and protein-cysteine to S-palmitoyl protein and CoA. Like ZDHHC1, ZDHHC5, ZDHHC6, ZDHHC7 and ZDHHC18 each contain one DHHC-type zinc finger through which they convey palmitoyltransferase activity against a broad range of substrates, including H-Ras, SNAP 25 and GABAA R proteins.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11625R-A750
Lokale Artikelnummer:: BOSSBS-11625R-A750
Beschreibung:   WW domain-binding protein 2 (WBP2) is a 261 amino acid protein expressed in most tissues. The WW domain is composed of 38 to 40 semi-conserved amino acids and is shared by various groups of proteins, including structural, regulatory and Signalling proteins. The domain mediates protein-protein interactions through the binding of polyproline ligands. WBP2 binds to the WW domain of Yes-associated protein (YAP), WW domain containing E3 ubiquitin protein ligase 1 (AIP5) and WW domain containing E3 ubiquitin protein ligase 2 (AIP2). The gene encoding WBP2 is located on human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes, some of which are involved in tumour suppression and in the pathogenesis of Li-Fraumeni syndrome, early onset breast cancer and a predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15324R-A555
Lokale Artikelnummer:: BOSSBS-15324R-A555
Beschreibung:   C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15324R-FITC)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15324R-FITC
Lokale Artikelnummer:: BOSSBS-15324R-FITC
Beschreibung:   C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15324R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15324R-CY3
Lokale Artikelnummer:: BOSSBS-15324R-CY3
Beschreibung:   C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:  1 * 100 µl
Lieferant:  Merck
Hersteller-Artikelnummer:: 1.06689.0100
Lokale Artikelnummer:: MERC1.06689.0100
Beschreibung:   Natriumdiethyldithiocarbamat Trihydrat ACS analytisches Reagens, Supelco®
VE:  1 * 100 g
Lieferant:  Resonac
Beschreibung:   Robust polymer-based HILIC column for saccharides.
New Product
Lieferant:  VWR Collection
Beschreibung:   Diese wiederverwendbaren Mäntel für Damen und Herren bestehen aus 63 % Polyester, 35 % Baumwolle und 2 % Kohlefaser, die für einen antistatischen Schutz sorgt. Alle Modelle verfügen über zweifach verstellbare Ärmelbündchen, zwei Seitentaschen, eine Brusttasche, einen Schneiderkragen und einen verdeckten Druckknopfverschluss.
Lieferant:  CHEMPUR
Beschreibung:   N-Chlorsuccinimid
Lieferant:  Lovibond Tintometer
Hersteller-Artikelnummer:: 19802650
Lokale Artikelnummer:: LOVI19802650
Beschreibung:   Accessory for UV/Visible spectrophotometers, Mixing cylinder, 25 ml
VE:  1 * 1 ST
Preis auf Anfrage
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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