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Bis(3-fluorphenyl)disulfid
Lieferant:
Alfa Aesar
Beschreibung:
Thymolblau Natriumsalz
Lieferant:
Brady
Beschreibung:
Durable, low-shrink vinyl with our most aggressive adhesive. Conforms to irregular, curved, rough and highly textured surfaces (painted cinder blocks, uneven wood, textured plastics, paper-jacketed pipes, powder-coated surfaces). Adheres to 'difficult' low-surface energy items (PVC piping, blow-molded equipment cases, ABS plastics, recycled plastics).
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
These medium gloves knitted from stainless steel, polyester, Lycra®, HPPE and glass fibre provide outstanding cut protection and enhanced durability.
Lieferant:
Alfa Aesar
Beschreibung:
Thymolblau Natriumsalz 0,04% (w/v) in wässriger Lösung
Artikel-Nr:
(BOSSBS-2604R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2604R-A680
Lokale Artikelnummer::
BOSSBS-2604R-A680
Beschreibung:
Receptor for interleukin-12. This subunit is the signaling component coupling to the JAK2/STAT4 pathway. Promotes the proliferation of T-cells as well as NK cells. Induces the promotion of T-cells towards the Th1 phenotype by strongly enhancing IFN-gamma production.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2604R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2604R-A750
Lokale Artikelnummer::
BOSSBS-2604R-A750
Beschreibung:
Receptor for interleukin-12. This subunit is the signaling component coupling to the JAK2/STAT4 pathway. Promotes the proliferation of T-cells as well as NK cells. Induces the promotion of T-cells towards the Th1 phenotype by strongly enhancing IFN-gamma production.
VE:
1 * 100 µl
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Die gestrickten Nylonhandschuhe mit Nitril-Schaum-Beschichtung an der Handfläche eignen sich besonders für trockene oder leicht ölige Anwendungen, die einen leichten mechanischen Schutz und ein Höchstmaß an Tastempfinden erfordern.
Artikel-Nr:
(BOSSBS-11457R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11457R-CY7
Lokale Artikelnummer::
BOSSBS-11457R-CY7
Beschreibung:
Receptor for the lysosphingolipid sphingosine 1-phosphate (S1P). S1P is a bioactive lysophospholipid that elicits diverse physiological effect on most types of cells and tissues. Is coupled to both the G(i/0)alpha and G(12) subclass of heteromeric G-proteins (By similarity). May play a regulatory role in the transformation of radial glial cells into astrocytes and may affect proliferative activity of these cells.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11457R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11457R
Lokale Artikelnummer::
BOSSBS-11457R
Beschreibung:
Receptor for the lysosphingolipid sphingosine 1-phosphate (S1P). S1P is a bioactive lysophospholipid that elicits diverse physiological effect on most types of cells and tissues. Is coupled to both the G(i/0)alpha and G(12) subclass of heteromeric G-proteins (By similarity). May play a regulatory role in the transformation of radial glial cells into astrocytes and may affect proliferative activity of these cells.
VE:
1 * 100 µl
Lieferant:
BIOTIX
Beschreibung:
Diese Einweg-Reservoirs wurden für Anwendungen mit Mehrkanalpipetten entwickelt und können mit Pipetten mit bis zu 12 Kanälen verwendet werden. Anwender können wählen zwischen opak weißen PVC-Reservoirs oder durchscheinenden PS-Reservoirs in verschiedenen Verpackungsausführungen.
Artikel-Nr:
(BOSSBS-9448R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-HRP
Lokale Artikelnummer::
BOSSBS-9448R-HRP
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 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-7969R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7969R-CY7
Lokale Artikelnummer::
BOSSBS-7969R-CY7
Beschreibung:
ARMC3 contains 12 ARM repeats. ARM (Armadillo/beta-catenin-like) domains are imperfect 45-amino acid repeats involved in protein-protein interactions. ARM domain-containing proteins, such as ARMC3, function in signal transduction, development, cell adhesion and mobility, and tumor initiation and metastasis. The specific function of ARMC3 is not yet known.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7969R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7969R
Lokale Artikelnummer::
BOSSBS-7969R
Beschreibung:
ARMC3 contains 12 ARM repeats. ARM (Armadillo/beta-catenin-like) domains are imperfect 45-amino acid repeats involved in protein-protein interactions. ARM domain-containing proteins, such as ARMC3, function in signal transduction, development, cell adhesion and mobility, and tumor initiation and metastasis. The specific function of ARMC3 is not yet known.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11034R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A350
Lokale Artikelnummer::
BOSSBS-11034R-A350
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 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-11034R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A750
Lokale Artikelnummer::
BOSSBS-11034R-A750
Beschreibung:
MYBPC1 is a 1141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 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-11034R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-CY3
Lokale Artikelnummer::
BOSSBS-11034R-CY3
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 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
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.
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