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1,8-Dihydroxynaphthalin
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15 226 results were found
1,8-Dihydroxynaphthalin
Artikel-Nr:
(BOSSBS-8218R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8218R-CY5
Lokale Artikelnummer::
BOSSBS-8218R-CY5
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-9675R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9675R-FITC
Lokale Artikelnummer::
BOSSBS-9675R-FITC
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 C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9675R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9675R-CY3
Lokale Artikelnummer::
BOSSBS-9675R-CY3
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 C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7740R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7740R-CY7
Lokale Artikelnummer::
BOSSBS-7740R-CY7
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-9676R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9676R-HRP
Lokale Artikelnummer::
BOSSBS-9676R-HRP
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-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
Artikel-Nr:
(BOSSBS-9676R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9676R-A647
Lokale Artikelnummer::
BOSSBS-9676R-A647
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-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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Acetamido-3-nitrobenzonitrile
Artikel-Nr:
(APOSOR470140-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR470140-5G
Lokale Artikelnummer::
APOSOR470140-5G
Beschreibung:
2-(Cyclopentyloxy)acetamide
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-9672R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9672R-A555
Lokale Artikelnummer::
BOSSBS-9672R-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 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-7740R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7740R-A680
Lokale Artikelnummer::
BOSSBS-7740R-A680
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-9675R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9675R-HRP
Lokale Artikelnummer::
BOSSBS-9675R-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 C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(521-3816)
Lieferant:
BECKMAN COULTER
Hersteller-Artikelnummer::
347824
Lokale Artikelnummer::
BECM347824
Beschreibung:
JA-18.1 Fixed angle (high performance) aluminium rotor, 24×1.8 ml microcentrifuge tubes, 18000 rpm, 42100×g. Includes 24 reversible adapters, for use in Avanti J Series centrifuges ( (except Avanti J-E).
VE:
1 * 1 ST
Lieferant:
Alfa Aesar
Beschreibung:
Trimethyl thiophosphate
Lieferant:
Bohlender
Beschreibung:
Silikon mit PTFE-Stulpe
Artikel-Nr:
(634-1231)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI634-1231
Beschreibung:
Das P9 UV/Vis-Doppelstrahl-Spektralphotometer ist ein anwenderfreundliches Gerät mit höherer Leistung.
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Thaxtomin A
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.
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.
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