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5-Brom-2-methoxyphenylborons\\u00E4ure


18 282  results were found

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Artikel-Nr: (BOSSBS-11329R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11329R-CY3
Lokale Artikelnummer:: BOSSBS-11329R-CY3
Beschreibung:   The ABL1 protooncogene encodes a cytoplasmic and nuclear protein tyrosine kinase that has been implicated in processes of cell differentiation, cell division, cell adhesion, and stress response. Activity of c-Abl protein is negatively regulated by its SH3 domain, and deletion of the SH3 domain turns ABL1 into an oncogene. The t(9;22) translocation results in the head-to-tail fusion of the BCR (MIM:151410) and ABL1 genes present in many cases of chronic myelogeneous leukemia. The DNA-binding activity of the ubiquitously expressed ABL1 tyrosine kinase is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function for ABL1. The ABL1 gene is expressed as either a 6- or 7-kb mRNA transcript, with alternatively spliced first exons spliced to the common exons 2-11. [provided by RefSeq].
VE:  1 * 100 µl
Lieferant:  Sigma-Aldrich
Beschreibung:   2,2-Dimethylpropan-1,3-diamin, Sigma-Aldrich®
Lieferant:  Sigma-Aldrich
Beschreibung:   4,4'-Dimethyl-2,2'-bipyridin, Sigma-Aldrich®
Lieferant:  BLD PHARMATECH GMBH
Beschreibung:   2,2′-Dimorpholinodiethylether 97%
Lieferant:  Sigma-Aldrich
Beschreibung:   2,2-Dimethoxy-2-phenylacetophenon, Sigma-Aldrich®
Lieferant:  Alfa Aesar
Beschreibung:   2-Methyl-2-propanyl-4-(aminomethyl)-1-piperidincarboxylat 97%
Lieferant:  MP Biomedicals
Beschreibung:   N,N'-Octamethylenebis(2,2-dichloroacetamide) is an inhibitor of aldehyde dehydrogenase, ALDH1A2.

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-10348R-A750
Lokale Artikelnummer:: BOSSBS-10348R-A750
Beschreibung:   The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure.
VE:  1 * 100 µl
Artikel-Nr: (BLDPBD53468-100G)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD53468-100G
Lokale Artikelnummer:: BLDPBD53468-100G
Beschreibung:   (±)-1,2-Hexandiol 97%
VE:  1 * 100 g
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   MAPK/ERK Signalling Pathway

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-10348R-A350
Lokale Artikelnummer:: BOSSBS-10348R-A350
Beschreibung:   The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8870R-FITC
Lokale Artikelnummer:: BOSSBS-8870R-FITC
Beschreibung:   The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8870R-HRP
Lokale Artikelnummer:: BOSSBS-8870R-HRP
Beschreibung:   The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Jul 2008].
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11914R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11914R
Lokale Artikelnummer:: BOSSBS-11914R
Beschreibung:   Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11914R-A750
Lokale Artikelnummer:: BOSSBS-11914R-A750
Beschreibung:   Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukaemias.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11914R-A680
Lokale Artikelnummer:: BOSSBS-11914R-A680
Beschreibung:   Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukaemias.
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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