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1,8-Dihydroxynaphthalin
Artikel-Nr:
(BOSSBS-7740R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7740R-A647
Lokale Artikelnummer::
BOSSBS-7740R-A647
Beschreibung:
CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8218R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8218R-A680
Lokale Artikelnummer::
BOSSBS-8218R-A680
Beschreibung:
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterisation.
VE:
1 * 100 µl
Lieferant:
VWR Chemicals
Beschreibung:
Ameisensäure ≥80%, TECHNICAL
Artikel-Nr:
(BOSSBS-9672R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9672R-A647
Lokale Artikelnummer::
BOSSBS-9672R-A647
Beschreibung:
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9672R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9672R-HRP
Lokale Artikelnummer::
BOSSBS-9672R-HRP
Beschreibung:
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.
VE:
1 * 100 µl
Lieferant:
RSG
Beschreibung:
Diese Klemmen mit Hülse bestehen aus elektrolytisch poliertem Edelstahl.
Artikel-Nr:
(LBCP7548600)
Lieferant:
LABCONCO
Hersteller-Artikelnummer::
7548600
Lokale Artikelnummer::
LBCP7548600
Beschreibung:
Rotor for 16×10 ml vials (Ø 18 mm × 65 mm), PTFE coated aluminium
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-7740R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7740R-A750
Lokale Artikelnummer::
BOSSBS-7740R-A750
Beschreibung:
CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8218R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8218R-A350
Lokale Artikelnummer::
BOSSBS-8218R-A350
Beschreibung:
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8218R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8218R-A555
Lokale Artikelnummer::
BOSSBS-8218R-A555
Beschreibung:
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9676R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9676R-A750
Lokale Artikelnummer::
BOSSBS-9676R-A750
Beschreibung:
MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localised genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
VE:
1 * 100 µl
Artikel-Nr:
(ABCAAB231774-1ML)
Lieferant:
Abcam
Beschreibung:
Anti-CD105 Rabbit Monoclonal Antibody [clone: EPR22811-18]
VE:
1 * 1 mL
New Product
Artikel-Nr:
(BOSSBS-2615R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2615R-A750
Lokale Artikelnummer::
BOSSBS-2615R-A750
Beschreibung:
Receptor for interleukin 18 (IL-18). Binding to the agonist leads to the activation of NF-kappa-B.
VE:
1 * 100 µl
Artikel-Nr:
(ABCAAB223293-1ML)
Lieferant:
Abcam
Beschreibung:
Anti-IL-18 Rabbit Monoclonal Antibody [clone: EPR22249-212]
VE:
1 * 1 mL
New Product
Artikel-Nr:
(221-0182)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI221-0182
Beschreibung:
Borosilikatglas 3.3.
VE:
1 * 2 ST
Artikel-Nr:
(BOSSBS-9653R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9653R
Lokale Artikelnummer::
BOSSBS-9653R
Beschreibung:
C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
VE:
1 * 100 µl
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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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