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2-Chloro-4-methylnicotinic+acid+ethyl+ester
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2-Chloro-4-methylnicotinic+acid+ethyl+ester
Artikel-Nr:
(BWRLBS1487)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS1487
Lokale Artikelnummer::
BWRLBS1487
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human Ubiquitin.
VE:
1 * 100 µG
Artikel-Nr:
(BWRLBS2644)
Lieferant:
Bioworld Technology
Hersteller-Artikelnummer::
BS2644
Lokale Artikelnummer::
BWRLBS2644
Beschreibung:
Synthetic peptide, corresponding to amino acids 11-60 of Human TACC1.
VE:
1 * 100 µG
Artikel-Nr:
(40022.)
Lieferant:
Biotium
Hersteller-Artikelnummer::
40022
Lokale Artikelnummer::
BTIU40022
Beschreibung:
CF® dye-dUTP can be used for TUNEL assay, microarray, or to synthesize labelled DNA probes for <i>in situ</i> hybridisation and nucleic acid blotting applications.
VE:
1 * 50 µl
Artikel-Nr:
(BOSSBS-8225R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8225R-FITC
Lokale Artikelnummer::
BOSSBS-8225R-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
Artikel-Nr:
(BOSSBS-8199R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-A555
Lokale Artikelnummer::
BOSSBS-8199R-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
Artikel-Nr:
(BOSSBS-8199R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-A350
Lokale Artikelnummer::
BOSSBS-8199R-A350
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:
VWR Collection
Beschreibung:
Transparente Polycarbonatbäder halten die Proben sichtbar, die Einheiten verfügen über einen benutzerfreundlichen MX-Temperaturregler mit drei Steuertasten und Anweisungen auf dem Bildschirm.
Artikel-Nr:
(APOSOR2923-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR2923-1G
Lokale Artikelnummer::
APOSOR2923-1G
Beschreibung:
2-Formylbenzene-1,4-disulphonate
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
3,3',5,5'-Tetra-tert-butyl-4,4'-diphenoquinone ≥98%
Artikel-Nr:
(BOSSBS-9659R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY5
Lokale Artikelnummer::
BOSSBS-9659R-CY5
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-9659R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY7
Lokale Artikelnummer::
BOSSBS-9659R-CY7
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-8409R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-A647
Lokale Artikelnummer::
BOSSBS-8409R-A647
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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. 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-11518R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11518R-CY7
Lokale Artikelnummer::
BOSSBS-11518R-CY7
Beschreibung:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11518R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11518R-CY3
Lokale Artikelnummer::
BOSSBS-11518R-CY3
Beschreibung:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl (E)-3-(2-pyridinyl)-2-propenoate
Artikel-Nr:
(APOSOR938169-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR938169-5G
Lokale Artikelnummer::
APOSOR938169-5G
Beschreibung:
3-Anilino-1-propanol 95%
VE:
1 * 5 g
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.
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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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