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5-Bromo-1,3-dimethyl-2-pyridone


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Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   1,3,3-Trimethyl-5-oxocyclohexanecarbonitrile
Artikel-Nr: (APOSOR301215-5G)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR301215-5G
Lokale Artikelnummer:: APOSOR301215-5G
Beschreibung:   5,6-Dibromo-2-pyridinamine 97%
VE:  1 * 5 g
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Methyl 2,4-dimethoxy-3-fluorobenzoate 95%
Artikel-Nr: (BOSSBS-4222R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4222R
Lokale Artikelnummer:: BOSSBS-4222R
Beschreibung:   Subunit of the 11S REG-gamma (also called PA28-gamma) proteasome regulator, a donut-shaped homoheptamer which associates with the proteasome. 11S REG-gamma activates the trypsin-like catalytic subunit of the proteasome but inhibits the chymotrypsin-like and postglutamyl-preferring (PGPH) subunits. Facilitates the MDM2-TP53/p53 interaction which promotes ubiquitination- and MDM2-dependent proteasomal degradation of TP53/p53, limiting its accumulation and resulting in inhibited apoptosis after DNA damage. May also be involved in cell cycle regulation.
VE:  1 * 100 µl
Lieferant:  Alfa Aesar
Beschreibung:   3,3'-Diaminobenzidin 99%
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8199R-FITC
Lokale Artikelnummer:: BOSSBS-8199R-FITC
Beschreibung:   FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8225R-A555
Lokale Artikelnummer:: BOSSBS-8225R-A555
Beschreibung:   FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8199R-A488
Lokale Artikelnummer:: BOSSBS-8199R-A488
Beschreibung:   FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8225R-A488
Lokale Artikelnummer:: BOSSBS-8225R-A488
Beschreibung:   FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:  1 * 100 µl
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   4-(Trifluoromethyl)-1H-benzimidazole
Artikel-Nr: (ANSE48-102/11)

Lieferant:  ANSELL HEALTH CARE
Hersteller-Artikelnummer:: 48-102/11
Lokale Artikelnummer:: ANSE48-102/11
Beschreibung:   Seamless knitted polyamide gloves with PU coating on palm and fingertips.
VE:  1 * 12 PAAR
Lieferant:  Thermo Scientific
Hersteller-Artikelnummer:: 193920100
Lokale Artikelnummer:: ACRO193920100
Beschreibung:   Rubidiumchlorid 99.99% (bezogen auf die Metalle der seltenen Erden)
VE:  1 * 10 g
Artikel-Nr: (BLDPBD65208-100MG)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD65208-100MG
Lokale Artikelnummer:: BLDPBD65208-100MG
Beschreibung:   Parthenolide 97% (durch HPLC)
VE:  1 * 100 mg
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Potassium (methoxymethyl)trifluoroborate
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Imidazo[1,2-a]pyrimidine-3-carboxylic acid
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   O-Methyl-L-tyrosine 97%
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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