Drucken
Sie suchten nach:
3 results were found
Ethyldiethoxyacetat
Artikel-Nr:
(BOSSBS-9497R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9497R-FITC
Lokale Artikelnummer::
BOSSBS-9497R-FITC
Beschreibung:
C9orf152 is a 239 amino acid protein encoded by a gene that maps to human chromosome 9q31.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0558R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0558R-CY5
Lokale Artikelnummer::
BOSSBS-0558R-CY5
Beschreibung:
Epithelial membrane protein-1 (EMP-1) is a four pass transmembrane protein consisting of 160 amino acids. It is a member of a small family of epithelial membrane proteins. EMP-1 is very similar in structure to its close relative, Peripheral Myelin Protein 22 (PMP22). It is most predominantly expressed in tissues of the gastrointestinal tract but has also been found to be a junctional protein in the liver expressed along the intercellular border. EMP-1 directly interacts with the C-terminus of the P2X7 receptor and may be involved in membrane blebbing. EMP-1 may also be an important regulator in cell communication, signaling, and adhesion. When EMP-1 is overexpressed, cell proliferation is inhibited, S phase is arrested and G1 phase is prolonged in esophogeal cancer cells. EMP-1 may play a role in tumorigenesis and has been identified as a biomarker for gefitinib treatment resistance for patients with lung cancer.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15344R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15344R
Lokale Artikelnummer::
BOSSBS-15344R
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf84 gene product has been provisionally designated C9orf84 pending further characterization. There are two isoforms of C9orf84 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15316R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15316R
Lokale Artikelnummer::
BOSSBS-15316R
Beschreibung:
C9orf16 (chromosome 9 open reading frame 16) is an 83 amino acid protein that belongs to the UPF0184 (EST00098) family and is encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15343R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15343R
Lokale Artikelnummer::
BOSSBS-15343R
Beschreibung:
C9orf79 is a 1,445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15313R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R
Lokale Artikelnummer::
BOSSBS-15313R
Beschreibung:
C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Lieferant:
BELLCO GLASS
Beschreibung:
Diese Fernbach-Kulturflaschen sind aus Borosilikatglas Typ 1, Klasse A.
Lieferant:
SCHURR SCHUHVERTRIEB
Beschreibung:
ESD-Sicherheitsschuh aus Mikrofaser Cordura®, DRYtech® -Futter mit Cambrelle®-Mesh-Einlage und einer rutschfesten und antistatischen ‚A4‘-Nitrilgummisohle; mit verstellbarem Fersenriemen.
Artikel-Nr:
(229-0737)
Lieferant:
KARTELL
Hersteller-Artikelnummer::
71252
Lokale Artikelnummer::
KART71252
Beschreibung:
PP, durchscheinend.
VE:
1 * 10 ST
Lieferant:
BROEN-LAB
Beschreibung:
Augenduschen zur Montage am Tisch. Mit einem oder zwei Duschköpfen im Winkel von 45°.
Artikel-Nr:
(BLEG516401)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
516401
Lokale Artikelnummer::
BLEG516401
Beschreibung:
Anti-IL-22 Goat Polyclonal Antibody [clone: Poly5164]
VE:
1 * 100 µG
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BLEG360802)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
360802
Lokale Artikelnummer::
BLEG360802
Beschreibung:
Anti-CXCL16 Mouse Monoclonal Antibody [clone: 22-19-12]
VE:
1 * 100 µG
This is a MarketSource item. Additional charges may apply
Lieferant:
HONEYWELL SAFETY
Beschreibung:
Wasserdichter Schnürschuh mit Obermaterial aus wasserabweisendem, geöltem Rauleder mit verstärktem Schutz an der Vorder- und Rückseite, gepolsterte Lasche und Zunge, seitlicher wasserdichter Federungskörper, 3-D-Futter und angespritzte PU2D-Laufsohle (gegen Temperaturschwankungen, Abrieb, Säuren und Basen in begrenzten bis niedrigen Konzentrationen beständig).
Artikel-Nr:
(J64071.MA)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J64071.MA
Lokale Artikelnummer::
ALFAJ64071.MA
Beschreibung:
Prima-1
VE:
1 * 10 mg
Lieferant:
Alfa Aesar
Beschreibung:
Eosin B
Artikel-Nr:
(USBI043777)
Lieferant:
US Biological
Hersteller-Artikelnummer::
043777
Lokale Artikelnummer::
USBI043777
Beschreibung:
Anti-VPS45 Rabbit Polyclonal Antibody
VE:
1 * 200 µl
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.
-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.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
