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8H-Indeno[1,2-c]thiophen-8-one
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8H-Indeno[1,2-c]thiophen-8-one
Artikel-Nr:
(BOSSBS-11589R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11589R
Lokale Artikelnummer::
BOSSBS-11589R
Beschreibung:
The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxC5 is a 222 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Existing as multiple alternatively spliced isoforms, HoxC5 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. The gene encoding HoxC5 maps to a cluster of Hox proteins on chromosome 12 that are essential for morphogenesis. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD134556-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD134556-500G
Lokale Artikelnummer::
BLDPBD134556-500G
Beschreibung:
Indigocarmin 85%
VE:
1 * 500 g
Artikel-Nr:
(BOSSBS-12345R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY7
Lokale Artikelnummer::
BOSSBS-12345R-CY7
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
VWR Collection
Beschreibung:
LDPE, Einweg. Durch Nutzung dieser unzerbrechlichen All-in-one-Pipetten werden Gefahren durch einen möglichen Glasbruch und durch Auslaufen infektiöser Materialien vermieden. Durch die Oberfläche mit geringer Affinität wird ein Verlust von Zellen und wertvollen Proteinen infolge der Bindung verringert. Die Pipetten sind ideal für alle Arbeiten, bei denen Flüssigkeiten schnell und sicher übertragen werden müssen.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Methylumbelliferyl-alpha-D-galactopyranoside
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2',3'-Difluor-4'-methylacetophenon 99%
Lieferant:
BURKLE
Beschreibung:
Novartos ist der pharmazeutische Zonensammler für die Probenahme gemäß den FDA-Richtlinien für Einheitsdosisproben. Mit den pharmazeutischen Probenehmern von Novartos können mehrere Einzeldosisproben (Einheitsdosisproben) von einer oder mehreren Probenahmestellen in einer einzigen Probenahme entnommen werden.
Artikel-Nr:
(BOSSBS-11589R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11589R-CY3
Lokale Artikelnummer::
BOSSBS-11589R-CY3
Beschreibung:
The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxC5 is a 222 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Existing as multiple alternatively spliced isoforms, HoxC5 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. The gene encoding HoxC5 maps to a cluster of Hox proteins on chromosome 12 that are essential for morphogenesis. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(NOVUNBP3-25663)
Lieferant:
Novus Biologicals
Hersteller-Artikelnummer::
NBP3-25663
Lokale Artikelnummer::
NOVUNBP3-25663
Beschreibung:
SARS-CoV-2 Nonstructural Protein 7 (NSP7) is one of the sixteen nonstructural proteins of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the causative agent of COVID-19 (1). SARS-CoV-2 NSP7 is 83 amino acids (aa) with a theoretical molecular weight of 9,2 kDa (1,2).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R
Lokale Artikelnummer::
BOSSBS-12345R
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY3
Lokale Artikelnummer::
BOSSBS-12345R-CY3
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY5
Lokale Artikelnummer::
BOSSBS-12345R-CY5
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11589R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11589R-CY7
Lokale Artikelnummer::
BOSSBS-11589R-CY7
Beschreibung:
The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxC5 is a 222 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Existing as multiple alternatively spliced isoforms, HoxC5 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. The gene encoding HoxC5 maps to a cluster of Hox proteins on chromosome 12 that are essential for morphogenesis. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-A680
Lokale Artikelnummer::
BOSSBS-12345R-A680
Beschreibung:
HEM1 is a 1127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-A750
Lokale Artikelnummer::
BOSSBS-12345R-A750
Beschreibung:
HEM1 is a 1127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(118-0549)
Lieferant:
PLUM HUDSIKKERHED
Hersteller-Artikelnummer::
5152
Lokale Artikelnummer::
PLUM5152
Beschreibung:
QuickStop ist als Druck-, Deck- und Stützverband universell einsetzbar. Das Set beinhaltet drei sterile Wundverbände mit integrierter Kompresse. Bei stärkeren Blutungen können die kleineren Wundverbände auch als zusätzliche Kompresse verwendet werden.
VE:
1 * 3 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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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