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5-Amino-2-nitrobenzoes\\\\u00E4ure


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Lieferant:  Sigma-Aldrich
Beschreibung:   3,5-Di-tert-butyl-4-hydroxybenzaldehyd Hemihydrat, Sigma-Aldrich®
Lieferant:  ABCR
Beschreibung:   Metal TMHD, Volatile Precursors for CVD

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11861R-A488
Lokale Artikelnummer:: BOSSBS-11861R-A488
Beschreibung:   HAP1 (huntingtin-associated protein 1) binds to huntingtin (1). Huntingtin is a protein that contains a polyglutamine region and when the number of glutamine repeats exceeds 35, the gene encodes a version of huntingtin that leads to Huntington’s disease (HD) (2,3). The ability of HAP1 to bind to huntingtin is enhanced by an expanded polyglutamine repeat region (1). HAP1 shows neuronal localization and moves with huntingtin in nerve fibers (4,5). HAP1 is primarily expressed in brain tissue, with greater expression in the olfactory bulb and brain stem (1). Mouse HAP1 is localized to membrane-bound organelles including large endosomes, tubulovesicular structures and budding vesicles in neurons (6). Duo, also designated huntingtin-associated protein interacting protein or HAPIP, binds Huntingtin-associated protein 1 (HAP1) and may have a role in vesicle trafficking and cytoskeletal function.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11733R-FITC
Lokale Artikelnummer:: BOSSBS-11733R-FITC
Beschreibung:   Myotubularin and the myotubularin-related proteins (MTMR1-9) belong to a highly conserved family of eukaryotic phosphatases. They are protein tyrosine phosphatases that utilize inositol phospholipids, rather than phosphoproteins, as substrates. MTMR family members hydrolyze both Phosphatidylinositol 3-phosphate (PtdIns3P) and PtdIns(3,5)P2. MTMR2 interacts with MTMR5, an inactive family member that increases the enzymatic activity of MTMR2 and dictates its subcellular localization. Mutations in MTMR2 cause autosomal recessive Charcot-Marie-Tooth type 4B1 (CMT4B1), which is characterized by reduced nerve conduction velocities, focally folded myelin sheaths and demyelination. MTMR3 and MTMR4 can either interact with each other or self associate. MTMR6 regulates the activity of the calcium-activated potassium channel 3.1. MTMR9 regulates the activity of MTMR7 and MTMR8.
VE:  1 * 100 µl
Lieferant:  HICHROM GAS CHROMATOGRAPHY
Beschreibung:   Proprietäre stationäre Phase mit niedriger Polarität und geringer Blutung; Gute Wahl für Pestizide, Herbizide, polychlorierte Biphenyle (PCBs) und polyaromatische Kohlenwasserstoffe (PAKs). Ideal für GC/MS-Anwendungen und auch eine ausgezeichnete Wahl als Bestätigungssäule für halbflüchtige Umweltanalysen.
Lieferant:  ABCR
Beschreibung:   Metal Beta-diketonates, Metal TMHD, Volatile Precursors for CVD
Lieferant:  MP Biomedicals
Beschreibung:   Colorimetric reagent for iron, manganese, titanium, and molybdenum. Complexing agent.
Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: D7283-1G
Lokale Artikelnummer:: SIALD7283-1G
Beschreibung:   3,5-Di-O-(p-toluyl)-2-deoxy-D-ribofuranosyl chloride ~90%, Sigma-Aldrich®
VE:  1 * 1 g
Lieferant:  Bernd Kraft
Beschreibung:   Kaliumchlorid 3.5 mol/l (3.5 N) in wässriger Lösung
Artikel-Nr: (BLDPBD208288-5G)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD208288-5G
Lokale Artikelnummer:: BLDPBD208288-5G
Beschreibung:   Ethyl-1-boc-3-azetidineacetate 97%
VE:  1 * 5 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9614R-A350
Lokale Artikelnummer:: BOSSBS-9614R-A350
Beschreibung:   Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9614R-A750
Lokale Artikelnummer:: BOSSBS-9614R-A750
Beschreibung:   Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder antitrypsin deficiency. This disorder is characterised by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterisation.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9614R-FITC
Lokale Artikelnummer:: BOSSBS-9614R-FITC
Beschreibung:   Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11733R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11733R-CY5
Lokale Artikelnummer:: BOSSBS-11733R-CY5
Beschreibung:   Myotubularin and the myotubularin-related proteins (MTMR1-9) belong to a highly conserved family of eukaryotic phosphatases. They are protein tyrosine phosphatases that utilize inositol phospholipids, rather than phosphoproteins, as substrates. MTMR family members hydrolyze both Phosphatidylinositol 3-phosphate (PtdIns3P) and PtdIns(3,5)P2. MTMR2 interacts with MTMR5, an inactive family member that increases the enzymatic activity of MTMR2 and dictates its subcellular localization. Mutations in MTMR2 cause autosomal recessive Charcot-Marie-Tooth type 4B1 (CMT4B1), which is characterized by reduced nerve conduction velocities, focally folded myelin sheaths and demyelination. MTMR3 and MTMR4 can either interact with each other or self associate. MTMR6 regulates the activity of the calcium-activated potassium channel 3.1. MTMR9 regulates the activity of MTMR7 and MTMR8.
VE:  1 * 100 µl
Lieferant:  Alfa Aesar
Beschreibung:   4-[(2,4-Dimethoxyphenyl)-(fmoc-amino)methyl]phenoxyacetic acid ≥98%
Lieferant:  Alfa Aesar
Beschreibung:   Excellent colorimetric substrate for detection of horseradish peroxidase labelled probes; particularly useful in ELISA techniques, blue result can be read spectrophotometrically at 370 or 650 nm3,3',5,5'-Tetramethylbenzidine is used as a clinical reagent for testing blood.
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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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