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Dimethyl+bicyclo[2.1.1]hexane-1,4-dicarboxylate
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Dimethyl+bicyclo[2.1.1]hexane-1,4-dicarboxylate
Artikel-Nr:
(PRSI4687P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
4687P
Lokale Artikelnummer::
PRSI4687P
Beschreibung:
CPEB1 peptide is used for blocking the activity of CPEB1 antibody.
VE:
1 * 50 µG
Lieferant:
ZEISS
Beschreibung:
Accessory for microscopes, Für: Axiostar, Strichkreuzmikrometer 14:140, Ø 26 mm
Artikel-Nr:
(PRSI3845P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
3845P
Lokale Artikelnummer::
PRSI3845P
Beschreibung:
RP105 peptide is used for blocking the activity of RP105 antibody.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI4951P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
4951P
Lokale Artikelnummer::
PRSI4951P
Beschreibung:
ZBTB1 peptide is used for blocking the activity of ZBTB1 antibody.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI3337P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
3337P
Lokale Artikelnummer::
PRSI3337P
Beschreibung:
Bcl-2 peptide is used for blocking the activity of Bcl-2 antibody.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI3943P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
3943P
Lokale Artikelnummer::
PRSI3943P
Beschreibung:
IRF7 peptide is used for blocking activity of IRF7 antibody.
VE:
1 * 50 µG
Artikel-Nr:
(BSBTA01127)
Lieferant:
BosterBio
Hersteller-Artikelnummer::
A01127
Lokale Artikelnummer::
BSBTA01127
Beschreibung:
Rabbit IgG polyclonal antibody for 14-3-3 sigma detection. Tested with WB, Direct ELISA in Human;Mouse;Rat.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-11984R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11984R-HRP
Lokale Artikelnummer::
BOSSBS-11984R-HRP
Beschreibung:
Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1G gives rise to T-type calcium currents. T-type calcium channels belong to the "low-voltage activated (LVA)" group and are strongly blocked by mibefradil. A particularity of this type of channels is an opening at quite negative potentials and a voltage-dependent inactivation. T-type channels serve pacemaking functions in both central neurons and cardiac nodal cells and support calcium signaling in secretory cells and vascular smooth muscle. They may also be involved in the modulation of firing patterns of neurons which is important for information processing as well as in cell growth processes. There are 2 isoforms of CACNA1H and 14 isoforms if CACNA1G, produced by alternative splicing.
VE:
1 * 100 µl
Artikel-Nr:
(539521-100)
Lieferant:
Merck Millipore (Oncogene)
Hersteller-Artikelnummer::
539521-100
Lokale Artikelnummer::
ONCO539521-100
Beschreibung:
Anti-PP2A/Balpha (14-27) (PR55) Rabbit Polyclonal Antibody
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9684R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9684R-FITC
Lokale Artikelnummer::
BOSSBS-9684R-FITC
Beschreibung:
C19orf54 is a 351 amino acid protein that exists as two alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9740R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9740R-HRP
Lokale Artikelnummer::
BOSSBS-9740R-HRP
Beschreibung:
CNTD2 (cyclin N-terminal domain containing 2) is a 155 amino acid protein that contains one cyclin N-terminal domain and is encoded by a gene that maps to human chromosome 19q13.2. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members, including killer cell and leukocyte Ig-like receptors, various ICAMs, the CEACAM and PSG families, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene Bcl-3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12567R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12567R-CY7
Lokale Artikelnummer::
BOSSBS-12567R-CY7
Beschreibung:
Bad is a member of the Bcl2 family and acts to promote apoptosis by forming heterodimers with the survival proteins Bcl2 and BclxL, thus preventing them from binding with BAX. Bad is found on the outer mitochondrial membrane and, once phosphorylated in response to growth stimuli, translocates to the cytoplasm. The phosphorylation status of Bad represents a key checkpoint for death or cell survival. JNK-induced phosphorylation of BAD serine 128 promotes the apoptotic role of Bad by opposing the inhibitory effect of growth factor on Bad-mediated apoptosis. Cdc2-induced phosphorylation of Bad serine 128 has an inhibitory effect on its interaction with 14-3-3 proteins. The latter interaction is critical for Bad phosphorylation at serine 155, a site within the BH3 domain that leads to the release of BclxL and the promotion of cell survival. Alternative splicing of this gene results in two transcript variants which encode the same isoform.This antibody recognise the phosphorylation site of human Ser75, mouse Ser111, rat Ser112.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12567R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12567R-A680
Lokale Artikelnummer::
BOSSBS-12567R-A680
Beschreibung:
Bad is a member of the Bcl2 family and acts to promote apoptosis by forming heterodimers with the survival proteins Bcl2 and BclxL, thus preventing them from binding with BAX. Bad is found on the outer mitochondrial membrane and, once phosphorylated in response to growth stimuli, translocates to the cytoplasm. The phosphorylation status of Bad represents a key checkpoint for death or cell survival. JNK-induced phosphorylation of BAD serine 128 promotes the apoptotic role of Bad by opposing the inhibitory effect of growth factor on Bad-mediated apoptosis. Cdc2-induced phosphorylation of Bad serine 128 has an inhibitory effect on its interaction with 14-3-3 proteins. The latter interaction is critical for Bad phosphorylation at serine 155, a site within the BH3 domain that leads to the release of BclxL and the promotion of cell survival. Alternative splicing of this gene results in two transcript variants which encode the same isoform. This antibody recognize the phosphorylation site of human Ser75, mouse Ser111, rat Ser112.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13605R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13605R-A350
Lokale Artikelnummer::
BOSSBS-13605R-A350
Beschreibung:
Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZNF206 (zinc finger protein 206), also known as ZSCAN10 (zinc finger and SCAN domain containing 10), is a 725 amino acid protein that contains one SCAN box domain and 14 C2H2-type zinc fingers. Localized to the nucleus, ZNF206 is thought to play a role in transcriptional regulation events. The gene encoding ZNF206 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
EPPENDORF
Beschreibung:
Adapter, für 14 Röhrchen 14 ml, 2 Stück, Für: Eppendorf 5804 / 5804 R / 5810 / 5810 R, Tisch-Zentrifuge
Artikel-Nr:
(SCOT286262206)
Lieferant:
DWK Life Sciences
Hersteller-Artikelnummer::
286262206
Lokale Artikelnummer::
SCOT286262206
Beschreibung:
Hergestellt aus DURAN®, Borosilikatglas 3.3, klar.
VE:
1 * 100 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.
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