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6-Chloro-4-methoxypyridazin-3-amine


18 282  results were found

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Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: CIL-PCB-174
Lokale Artikelnummer:: PROOCIL-PCB-174
Beschreibung:   Organic Standard, 2,2',3,3',4,5,6'-Heptachlorbiphenyl (PCB Nr. 174) 35 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 1 mL
Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: CIL-PCB-187
Lokale Artikelnummer:: PROOCIL-PCB-187
Beschreibung:   Organic Standard, 2,2',3,4',5,5',6-Heptachlorbiphenyl (PCB Nr. 187) 35 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 1 mL
Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: CIL-PCB-135
Lokale Artikelnummer:: PROOCIL-PCB-135
Beschreibung:   Organic Standard, 2,2',3,3',5,6'-Hexachlorbiphenyl (PCB Nr. 135) 35 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 1 mL
Artikel-Nr: (548-1327)

Lieferant:  CHROMACOL
Hersteller-Artikelnummer:: T-28
Lokale Artikelnummer:: CRMAT-28
Beschreibung:   These vial racks are chemically resistant and fairly robust for a safe working position on the lab bench and during transport.
VE:  1 * 5 ST
Lieferant:  Simport Scientific
Hersteller-Artikelnummer:: M965-40
Lokale Artikelnummer:: SIMPM965-40
Beschreibung:   Der CytoSep™ MEGA Trichter bietet eine einfache, effiziente und kostengünstige Möglichkeit zur Herstellung von hochwertigen Dünnschicht-Objektträgerpräparaten. Edelstahlklemmen sind nicht länger erforderlich, wodurch der Arbeitsablauf im Labor verbessert wird. Er eignet sich für die bequeme Vorbereitung von größeren Probenvolumen. Dieser größere Trichter ist schnell und einfach zu entfernen. Der große rechteckige Aufbringbereich für Zellen von 22×14,75 mm (325 mm²) ermöglicht ein 12-mal größeres Probenvolumen (6 ml) im Vergleich zum einfachen CytoSep™ Zytologie-Trichter. Mit ihm lassen sich im Vergleich zu anderen Dünnschichtmethoden kostengünstigere Dünnschicht-Präparate herstellen. Strategisch platzierte Leitbleche verhindern die Zellablagerung, so dass eine gleichmäßige Zellverteilung erreicht wird und damit hochwertige Objektträgerpräparate erstellt werden. CytoSep™ MEGA Zytologie-Trichter mit Deckel minimieren den Kontakt der Benutzer mit Pathogenen und verringern die Gefahr einer Kreuzkontamination der Proben. Zur Vorbereitung von lufttrockenen und fixierten Präparaten.
VE:  1 * 480 ST

Lieferant:  ProSci Inc.
Hersteller-Artikelnummer:: 4231P
Lokale Artikelnummer:: PRSI4231P
Beschreibung:   TBC1D1 peptide is used for blocking the activity of TBC1D1 antibody.
VE:  1 * 50 µG

Lieferant:  ProSci Inc.
Hersteller-Artikelnummer:: 2489
Lokale Artikelnummer:: PRSI2489
Beschreibung:   IL-22 Receptor Antibody: A novel cytokine, designated IL-TIF for IL-10 related T cell-derived inducible factor and IL-22, was recently identified. The receptor for IL-22 (IL-22R, also termed CRF2-9 and IL-TIF-R1 chain) is a new member of the class II cytokine receptor family. IL-22R forms a complex with IL-10 receptor beta chain and mediates IL-22 signaling. IL-22 and its receptor activate JAK-STAT signaling pathway. IL22R is expressed in normal liver and kidney and their cell lines HepG2 and TK-10. A soluble form of IL-22 receptor, also termed IL-22 binding protein (IL-22BP) and IL-22 receptor-alpha 2 (IL-22RA2), was identified very recently. IL-22BP prevents binding of IL-22 to the functional cell surface IL-22R complex and neutralizes IL-22 activity. LPS induces IL-22 expression, which indicates the role of IL-22 in inflammatory response.
VE:  1 * 100 µG

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9747R-A647
Lokale Artikelnummer:: BOSSBS-9747R-A647
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. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases 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 characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, 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-15318R-A647
Lokale Artikelnummer:: BOSSBS-15318R-A647
Beschreibung:   C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 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: (BOSSBS-9174R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9174R-CY5.5
Lokale Artikelnummer:: BOSSBS-9174R-CY5.5
Beschreibung:   Tripartite motif-containing protein 3 (TRIM3), also known as RING finger protein 22 (RNF22), RING finger protein 97 (RNF97) or brain-expressed RING finger protein (BERP), is a 744 amino acid member of the TRIM family, also known as the RING-B-box coiled-coil (RBCC) family. Members of the RBCC family have an N-terminal RING finger, followed by one or two zinc-binding domains (B-box domains), a leucine coiled-coil region and a variable C-terminal domain. Localized to cytoplasmic filaments, TRIM3 has been shown to interact with å-actinin-4 and myosin V, two proteins associated with the actin cytoskeleton. Specifically, å-actinin-4 interacts with the RBCC domain of TRIM3, and the C-terminal tail of Myosin V interacts with with the unique C-terminal ∫-propeller domain of TRIM3. These associations suggest that TRIM3 may play a role in cell motility and cargo transport. Three named isoforms of TRIM3 exist as a result of alternative splicing events.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15330R-FITC)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15330R-FITC
Lokale Artikelnummer:: BOSSBS-15330R-FITC
Beschreibung:   C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 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:  Bioss
Hersteller-Artikelnummer:: BS-15314R-A488
Lokale Artikelnummer:: BOSSBS-15314R-A488
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: (BLEG576209)

Lieferant:  BIOLEGEND INC
Hersteller-Artikelnummer:: 576209
Lokale Artikelnummer:: BLEG576209
Beschreibung:   ELISA Standard 4-Pack contains four vials of recombinant mouse IL-22 at >5 ng per vial. Recommended for ELISA application only. Standards are calibrated against a BioLegend Master Calibrator.
VE:  1 * 1 Pack.
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: CIL-PCB-194-CS
Lokale Artikelnummer:: PROOCIL-PCB-194-CS
Beschreibung:   Organic Standard, 2,2',3,3',4,4',5,5'-Octachlorbiphenyl (PCB Nr. 194) 100 µg/ml in Isooctan, Packung: Glasflasche
VE:  1 * 1,2 mL
Lieferant:  DICKSON
Beschreibung:   Diagramm für Schreiber, C320, +22...+68 °F

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15350R-A647
Lokale Artikelnummer:: BOSSBS-15350R-A647
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
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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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