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(±)11(12)-EET+methyl+ester
Artikel-Nr:
(BOSSBS-8076R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A647
Lokale Artikelnummer::
BOSSBS-8076R-A647
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A488
Lokale Artikelnummer::
BOSSBS-8076R-A488
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-A750
Lokale Artikelnummer::
BOSSBS-8076R-A750
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognized for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8076R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8076R-CY7
Lokale Artikelnummer::
BOSSBS-8076R-CY7
Beschreibung:
ARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain-containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localised, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. The ARRDC2 and ARRDC5 genes map to chromosome 19, which consists of over 63 million bases, houses approximately 1,400 genes and is recognised for having the greatest gene density of the human chromosomes. Unlike other ARRDC genes, the ARRDC4 gene maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localised genes.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Acetamido-5-carboxyphenylboronsäure 98%
Lieferant:
Alfa Aesar
Beschreibung:
Rhenium ≥99,97% (Metall-Basis), Drahtform, Ø 0.5 mm (0.02 in)
Artikel-Nr:
(BOSSBS-8242R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-CY3
Lokale Artikelnummer::
BOSSBS-8242R-CY3
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8242R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8242R-CY7
Lokale Artikelnummer::
BOSSBS-8242R-CY7
Beschreibung:
CTDSPL2 (CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2), also known as HSPC058 or HSPC129, is a 466 amino acid protein that contains one FCP1 homology domain and belongs to the CTDSPL2 family. Existing as two alternatively spliced isoforms, CTDSPL2 is thought to function as a phosphatase and is encoded by a gene that maps to human chromosome 15q15.3. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
VE:
1 * 100 µl
Lieferant:
Merck
Beschreibung:
Im Allgemeinen bestehen Ionenaustauscher aus einer quervernetzten Polymermatrix mit einer gleichmäßigen Verteilung fester Ionenansammlungen über die Harzstruktur hinweg. Diese müssen durch eine äquivalente Anzahl von Ionen mit entgegengesetzter Ladung, den Gegenionen, im Gleichgewicht gehalten werden, um die elektrische Neutralität zu erhalten. Kationenaustauscher können daher nur Kationen austauschen und anreichern, Anionenaustauscher nur Anionen. Adsorberharze besitzen im Gegensatz dazu einen nicht-ionischen, jedoch je nach Aufbau mehr oder weniger polaren Charakter und adsorbieren nichtstöchiometrisch Anionen, Kationen als auch ungeladene Verbindungen.
Lieferant:
Alfa Aesar
Beschreibung:
Stab. with 0.1% potassium hydroxide
Artikel-Nr:
(SIAL272477-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
272477-5G
Lokale Artikelnummer::
SIAL272477-5G
Beschreibung:
3-Brompropionaldehyddimethylacetal, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(BLDPBD74083-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD74083-1G
Lokale Artikelnummer::
BLDPBD74083-1G
Beschreibung:
6-Fluor-2-pyridincarbonitril 97%
VE:
1 * 1 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Ytterbium(III)iodid, Sigma-Aldrich®
Lieferant:
VARIAN
Beschreibung:
Bond Elut™ Focus solid phase extraction cartridges with enhanced polar recovery. Features a unique amide functionalised polar-enhanced sorbent technology that delivers outstanding retention for polar and non-polar analytes.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Cyclopropyl-isoxazole-3-carboxylic acid 95%
Lieferant:
Thermo Scientific
Beschreibung:
Diisobutylaluminiumhydrid 1.0 M in Heptan, AcroSeal™
Preis auf Anfrage
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 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.
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