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4,4\'-Dibrom-2,2\'-bipyridin


30 929  results were found

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Artikel-Nr: (BOSSBS-15314R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15314R-CY5
Lokale Artikelnummer:: BOSSBS-15314R-CY5
Beschreibung:   C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. 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:  Bioss
Hersteller-Artikelnummer:: BS-15314R-A750
Lokale Artikelnummer:: BOSSBS-15314R-A750
Beschreibung:   C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. 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:  Bioss
Hersteller-Artikelnummer:: BS-15314R-A647
Lokale Artikelnummer:: BOSSBS-15314R-A647
Beschreibung:   C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. 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: (BSANBS-010117-FK)

Lieferant:  BIOSAN
Hersteller-Artikelnummer:: BS-010117-FK
Lokale Artikelnummer:: BSANBS-010117-FK
Beschreibung:   PRS-22 Platform, standard, can accommodate 22 tubes, 10 - 16 mm diameter (1,5 - 15 ml tubes)
VE:  1 * 1 ST
Artikel-Nr: (BOSSBS-15350R-HRP)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15350R-HRP
Lokale Artikelnummer:: BOSSBS-15350R-HRP
Beschreibung:   C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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:  Alfa Aesar
Beschreibung:   A substrate used for the determination of D-glucosidase.
Artikel-Nr: (ICNA04805732)

Lieferant:  MP Biomedicals
Hersteller-Artikelnummer:: 04805732
Lokale Artikelnummer:: ICNA04805732
Beschreibung:   Bromophenol blue is a tracking dye for alkaline and neutral buffer systems. It is used as a tracking dye in DNA, RNA (agarose) and protein (polyacrylamide) gel electrophoresis.
VE:  1 * 10 g
Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR52944-5G
Lokale Artikelnummer:: APOSOR52944-5G
Beschreibung:   5-(5-Chlorosulphonyl-2-ethoxyphenyl)-1-methyl-3-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one 98%
VE:  1 * 5 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15350R-A680
Lokale Artikelnummer:: BOSSBS-15350R-A680
Beschreibung:   C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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:  US Biological
Hersteller-Artikelnummer:: 135333
Lokale Artikelnummer:: USBI135333
Beschreibung:   Anti-WBSCR22 Mouse Polyclonal Antibody
VE:  1 * 50 µG
Lieferant:  BIOLEGEND INC
Beschreibung:   Human recombinant IL-22 (from <i>E. coli</i>)
Artikel-Nr: (114-4467)

Lieferant:  Portwest Clothing
Hersteller-Artikelnummer:: SK33BKR44-48
Lokale Artikelnummer:: PRTWSK33BKR44-48
Beschreibung:   Diese Strümpfe bestehen aus 79 % Acryl, 15 % Nylon und 6 % Polyester.
VE:  1 * 3 PAAR

Lieferant:  BIOLEGEND INC
Hersteller-Artikelnummer:: 716202
Lokale Artikelnummer:: BLEG716202
Beschreibung:   Human recombinant IL-22 (from <i>E. coli</i>)
VE:  1 * 10 µG
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  Sampling Systems
Beschreibung:   Solid sampler, Sample insert, stainless steel, 2,2 ml
Lieferant:  Merck Millipore (Oncogene)
Hersteller-Artikelnummer:: NE1015-100
Lokale Artikelnummer:: ONCONE1015-100
Beschreibung:   Anti-Glial Fibrillary Acidic Protein Cocktail (SMI-22) Mouse Monoclonal Antibody [clone: SMI-22]
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-0558R-A350
Lokale Artikelnummer:: BOSSBS-0558R-A350
Beschreibung:   Epithelial membrane protein-1 (EMP-1) is a four pass transmembrane protein consisting of 160 amino acids. It is a member of a small family of epithelial membrane proteins. EMP-1 is very similar in structure to its close relative, Peripheral Myelin Protein 22 (PMP22). It is most predominantly expressed in tissues of the gastrointestinal tract but has also been found to be a junctional protein in the liver expressed along the intercellular border. EMP-1 directly interacts with the C-terminus of the P2X7 receptor and may be involved in membrane blebbing. EMP-1 may also be an important regulator in cell communication, signaling, and adhesion. When EMP-1 is overexpressed, cell proliferation is inhibited, S phase is arrested and G1 phase is prolonged in esophogeal cancer cells. EMP-1 may play a role in tumorigenesis and has been identified as a biomarker for gefitinib treatment resistance for patients with lung cancer.
VE:  1 * 100 µl
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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