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(\\\\\\\\u00B1)11(12)-EET+methyl+ester
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(\\\\\\\\u00B1)11(12)-EET+methyl+ester
Artikel-Nr:
(BOSSBS-11518R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11518R
Lokale Artikelnummer::
BOSSBS-11518R
Beschreibung:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.
VE:
1 * 100 µl
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese gestrickten Lycra®/Kevlar®-Träger mit Nitrilschaumbeschichtung auf der Handinnenseite sind schnitt- und hitzebeständig und vielseitig einsetzbar.
Artikel-Nr:
(BOSSBS-8225R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-A750
Lokale Artikelnummer::
BOSSBS-8225R-A750
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-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-CY5
Lokale Artikelnummer::
BOSSBS-8199R-CY5
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-8225R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-CY5.5
Lokale Artikelnummer::
BOSSBS-8225R-CY5.5
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-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-CY7
Lokale Artikelnummer::
BOSSBS-8199R-CY7
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-8225R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-CY7
Lokale Artikelnummer::
BOSSBS-8225R-CY7
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-3223R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3223R
Lokale Artikelnummer::
BOSSBS-3223R
Beschreibung:
HSL/LIPE is found in adipose tissue and heart, where it primarily hydrolyzes stored triglycerides to free fatty acids. It is also found in steroidogenic tissues, where it principally converts cholesteryl esters to free cholesterol for steroid hormone production. There are two named isoforms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11888R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11888R-A350
Lokale Artikelnummer::
BOSSBS-11888R-A350
Beschreibung:
MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. 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 stranded 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.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD8761-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD8761-25G
Lokale Artikelnummer::
BLDPBD8761-25G
Beschreibung:
4'-Benzyloxy-3'-methoxyacetophenon 97%
VE:
1 * 25 g
Lieferant:
Alfa Aesar
Beschreibung:
2-Phenylbenzoesäure ≥98%
Artikel-Nr:
(BLDPBD242749-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD242749-250MG
Lokale Artikelnummer::
BLDPBD242749-250MG
Beschreibung:
4,6-Dimethylpicolinonitrile 95%
VE:
1 * 250 mg
Artikel-Nr:
(BOSSBS-9941R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9941R-A750
Lokale Artikelnummer::
BOSSBS-9941R-A750
Beschreibung:
C11orf71, also known as FLJ20010, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 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 _ thalassemia are caused by HBB gene mutations. Wilms' tumours, 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:
tert-Butyl-2,6-diazaspiro[3.3]heptane-2-carboxylate oxalate 95%
Artikel-Nr:
(BOSSBS-9659R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY5.5
Lokale Artikelnummer::
BOSSBS-9659R-CY5.5
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:
(METOGRU2436S)
Lieferant:
Metro International
Hersteller-Artikelnummer::
GRU2436S
Lokale Artikelnummer::
METOGRU2436S
Beschreibung:
Racks are designed to provide efficient storage of cleanroom garments. The hangers are spaced at 75 mm intervals.
VE:
1 * 1 ST
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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