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1,2-Phenylendiisothiocyanat


37 646  results were found

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Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: PC31870-250MG
Lokale Artikelnummer:: APOSPC31870-250MG
Beschreibung:   3-(2-Chloro-6-fluorophenyl)-N-(2-{[(fur-2-yl)methyl]sulphanyl}ethyl)-5-methylisoxazole-4-carboxamide
VE:  1 * 250 mg
Artikel-Nr: (BOSSBS-11324R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11324R-CY3
Lokale Artikelnummer:: BOSSBS-11324R-CY3
Beschreibung:   Nova-1 and Nova-2 are members of a superfamily of protein regulators of RNA metabolism in neurons. Both are nuclear RNA binding proteins with K homology motifs, conserved protein sequences which bind to RNA (1,2). Nova proteins, normally sequestered in the central nervous system, are expressed by systemic tumors in patients with the autoimmune disorder paraneoplastic opsoclonus-myoclonus ataxia (POMA) (3,4). Nova-1 is expressed in the hindbrain and ventral spinal cord and Nova-2 is expressed in the neocortex and hippocampus (4). Nova-1 is necessary for regulating neuron-specific alternative splicing of the glycine receptor Alpha2 pre-mRNA (5).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-3743R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-3743R
Lokale Artikelnummer:: BOSSBS-3743R
Beschreibung:   This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-12920R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12920R
Lokale Artikelnummer:: BOSSBS-12920R
Beschreibung:   This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15130R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15130R
Lokale Artikelnummer:: BOSSBS-15130R
Beschreibung:   The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11324R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11324R-CY5
Lokale Artikelnummer:: BOSSBS-11324R-CY5
Beschreibung:   Nova-1 and Nova-2 are members of a superfamily of protein regulators of RNA metabolism in neurons. Both are nuclear RNA binding proteins with K homology motifs, conserved protein sequences which bind to RNA (1,2). Nova proteins, normally sequestered in the central nervous system, are expressed by systemic tumors in patients with the autoimmune disorder paraneoplastic opsoclonus-myoclonus ataxia (POMA) (3,4). Nova-1 is expressed in the hindbrain and ventral spinal cord and Nova-2 is expressed in the neocortex and hippocampus (4). Nova-1 is necessary for regulating neuron-specific alternative splicing of the glycine receptor Alpha2 pre-mRNA (5).
VE:  1 * 100 µl
Lieferant:  COMBI-BLOCKS
Beschreibung:   1,2-Dichlor-3-iodbenzol
Lieferant:  FLUOROCHEM
Beschreibung:   1,2-Dichlor-3-iodbenzol
Artikel-Nr: (SPCMM1177-25ML)

Lieferant:  Spectrum Chemical
Hersteller-Artikelnummer:: M1177-25ML
Lokale Artikelnummer:: SPCMM1177-25ML
Beschreibung:   Monothioglycerol, also known as 3-Mercaptopropane-1,2-diol and thioglycerol, is often used as a matrix in liquid secondary ion mass spectrometry and fast atom bombardment mass spectrometry.
VE:  1 * 25 mL
Lieferant:  BIONET RESEARCH
Beschreibung:   5-Methylimidazo[1,2-a]pyridin
Lieferant:  FLUOROCHEM
Hersteller-Artikelnummer:: 019182-25G
Lokale Artikelnummer:: FLUO019182-25G
Beschreibung:   1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-Heneicosafluor-12-ioddodecan
VE:  1 * 25 g
Market Source Item This is a MarketSource item. Additional charges may apply

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8346R-A488
Lokale Artikelnummer:: BOSSBS-8346R-A488
Beschreibung:   FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8346R-FITC
Lokale Artikelnummer:: BOSSBS-8346R-FITC
Beschreibung:   FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12303R-HRP
Lokale Artikelnummer:: BOSSBS-12303R-HRP
Beschreibung:   Hemogen is a 484 amino acid protein encoded by the human gene HEMGN. Hemogen is a nuclear protein that is expressed in hematopoietic precursor cells and can be detected in CD34+ and K-562 leukemia cell line. It is also expressed in bone marrow, testis, thymus and thyroid tumors, non-Hodgkin lymphoma, various leukemia cell lines, peripheral blood mononuclear cells (PBMCs) and bone marrow mononuclear cells (BMMCs) of patients with leukemia. Hemogen is down-regulated during megakaryocytic differentiation of K-562 cells by 12-O-tetradecanoylphorbol-13-acetate (TPA) (at protein level). It can be up-regulated in normal PBMCs by mitogens.
VE:  1 * 100 µl
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   6-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amine
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11255R-FITC
Lokale Artikelnummer:: BOSSBS-11255R-FITC
Beschreibung:   Several protein-protein interactions are essential to membrane fusion during endocytosis. Membrane fusion requires interaction among SNARE1 proteins associated with both donor and acceptor membranes (1,2). Following membrane fusion, the α-SNAP cytoplasmic adapter protein binds to the SNARE complex. N-ethylmaleimide-sensitive factor (NSF), a hexameric ATPase, then associates with the α-SNAP/SNARE complex to mediate SNARE disassembly during membrane fusion (3,4). The ATPase activity of NSF induces a conformational change in the α-SNAP/SNARE complex that leads to its dissociation from the membrane, membrane fusion and eventual recycling of the SNARE complex for subsequent membrane fusion (3,4).
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.
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