Suche >
2-(Trifluoromethyl)quinoline
Drucken
Sie suchten nach:
128 811 results were found
2-(Trifluoromethyl)quinoline
Artikel-Nr:
(BOSSBS-8225R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R
Lokale Artikelnummer::
BOSSBS-8225R
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
Artikel-Nr:
(BOSSBS-8199R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-CY3
Lokale Artikelnummer::
BOSSBS-8199R-CY3
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
Artikel-Nr:
(BOSSBS-9659R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A555
Lokale Artikelnummer::
BOSSBS-9659R-A555
Beschreibung:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6758R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6758R-CY7
Lokale Artikelnummer::
BOSSBS-6758R-CY7
Beschreibung:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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, while 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-encoded genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13190R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13190R-FITC
Lokale Artikelnummer::
BOSSBS-13190R-FITC
Beschreibung:
Fas ligand associated factor 1; Fas ligand-associated factor 1; FBP 11; FBP11; FLAF 1; FLAF1; FNBP 3; Formin binding protein 11; Formin binding protein 3; Formin-binding protein 11; Formin-binding protein 3; HIP-10; HIP10; Huntingtin interacting protein A; Huntingtin interacting protein HYPA; Huntingtin yeast partner A; Huntingtin-interacting protein 10; Huntingtin-interacting protein A; HYPA; NY REN 6; NY REN 6 antigen; PR40A_HUMAN; Pre mRNA processing factor 40 homolog A; Pre-mRNA-processing factor 40 homolog A; PRP40 pre mRNA processing factor 40 homolog A (S cerevisiae); PRP40 pre mRNA processing factor 40 homolog A (yeast); PRP40 pre mRNA processing factor 40 homolog A; PRPF 40A; PRPF40A; Renal carcinoma antigen NY-REN-6.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6758R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6758R-A647
Lokale Artikelnummer::
BOSSBS-6758R-A647
Beschreibung:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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, while 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-encoded genes.
VE:
1 * 100 µl
Artikel-Nr:
(BWRLBS3546)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS3546
Lokale Artikelnummer::
BWRLBS3546
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human Insulin.
VE:
1 * 100 µG
Artikel-Nr:
(BWRLBS5529)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS5529
Lokale Artikelnummer::
BWRLBS5529
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human p53.
VE:
1 * 100 µG
Artikel-Nr:
(462-0205)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRIMX-CV12
Beschreibung:
The MX immersion thermostat is user friendly with three control buttons and on-screen prompts. The convenient slide control enables the flow rate to be easily adjusted, and it can clamp securely to straight or curved tank walls.
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,2'-Dithiodianilin (Thulium-Ionophor I) 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,3'-Dihydroxybenzidine 97%
Artikel-Nr:
(BOSSBS-11518R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11518R-CY5
Lokale Artikelnummer::
BOSSBS-11518R-CY5
Beschreibung:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.
VE:
1 * 100 µl
Artikel-Nr:
(1A01300.)
Lieferant:
USP
Hersteller-Artikelnummer::
1A01300
Lokale Artikelnummer::
USPH1A01300
Beschreibung:
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
VE:
1 * 25 mg
Artikel-Nr:
(BLDPBD95762-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD95762-100MG
Lokale Artikelnummer::
BLDPBD95762-100MG
Beschreibung:
4-Chloro-2-(methylsulphonyl)pyrimidine 98%
VE:
1 * 100 mg
Lieferant:
Thermo Scientific
Beschreibung:
Methylenblau Hydrat 96+%, hochrein biologische Färbemittel
Artikel-Nr:
(BOSSBS-9659R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY3
Lokale Artikelnummer::
BOSSBS-9659R-CY3
Beschreibung:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Preis auf Anfrage
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
 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
