Your search request has been modified to limit number of results. Your search was - N\\\'-[1-Cyclopropylaminopropylidene]hydrazinecarboxylic+acid-tert-b |
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Artikel-Nr:
(BOSSBS-11406R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-CY5
Lokale Artikelnummer::
BOSSBS-11406R-CY5
Beschreibung:
GIOT-1 is a 563 amino acid protein belonging to the Krüppel C2H2-type zinc-finger protein family. Localized to the nucleus, GIOT-1 is widely expressed in tissues, with highest levels in liver, kidney, small intestine, pancreas and thymus. GIOT-1 contains 12 C2H2-type zinc fincers and one KRAB domain. Because the KRAB domain functions as a transcriptional repressor when attached to the template DNA, GIOT-1 is thought to be involved in transcriptional regulation. The gene encoding GIOT-1 is localized to chromosome 19q13.12 and two isoforms of GIOT-1 exist as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12919R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-A647
Lokale Artikelnummer::
BOSSBS-12919R-A647
Beschreibung:
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-CY3
Lokale Artikelnummer::
BOSSBS-15130R-CY3
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9982R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9982R-A750
Lokale Artikelnummer::
BOSSBS-9982R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11190R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11190R-HRP
Lokale Artikelnummer::
BOSSBS-11190R-HRP
Beschreibung:
C9 is a plasma protein synthesized in the liver and monocytes consisting of a single polypeptide chain. C9 is a part of the membrane attack complex (MAC), an important component of the immune system. The MAC forms upon complement system activation by invading pathogenic bacteria and consists of the four major complement proteins: C5b, C6, C7 and C8. These complement proteins bind to the outer surface of the plasma membrane of the invading cell. C9 binds to the membrane associated C5b-8 protein, which leads to the circular polymerization of 12-18 C9 molecules. These polymerized C9 molecules form a ring structure in the membrane. Molecules can then diffuse freely through this transmembrane channel, causing cell lysis and destruction of the invading bacterial cell.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15307R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15307R-CY5
Lokale Artikelnummer::
BOSSBS-15307R-CY5
Beschreibung:
C9 is a plasma protein synthesised in the liver and monocytes consisting of a single polypeptide chain. C9 is a part of the membrane attack complex (MAC), an important component of the immune system. The MAC forms upon complement system activation by invading pathogenic bacteria and consists of the four major complement proteins: C5b, C6, C7 and C8. These complement proteins bind to the outer surface of the plasma membrane of the invading cell. C9 binds to the membrane associated C5b-8 protein, which leads to the circular polymerisation of 12-18 C9 molecules. These polymerised C9 molecules form a ring structure in the membrane. Molecules can then diffuse freely through this transmembrane channel, causing cell lysis and destruction of the invading bacterial cell.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9584R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9584R-CY7
Lokale Artikelnummer::
BOSSBS-9584R-CY7
Beschreibung:
Membrane receptor signaling by various ligands, including interferons and growth hormones such as EGF, induces activation of JAK kinases which then leads to tyrosine phosphorylation of the various Stat transcription factors. Stat1 and Stat2 are induced by IFN-å and form a heterodimer which is part of the ISGF3 transcription factor complex. Although early reports indicate Stat3 activation by EGF and IL-6, it has been shown that Stat3∫ appears to be activated by both while Stat3å is activated by EGF, but not by IL-6. Highest expression of Stat4 is seen in testis and myeloid cells. IL-12 has been identified as an activator of Stat4. Stat5 has been shown to be activated by Prolactin and by IL-3. Stat6 is involved in IL-4 activated signaling pathways.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15307R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15307R
Lokale Artikelnummer::
BOSSBS-15307R
Beschreibung:
C9 is a plasma protein synthesized in the liver and monocytes consisting of a single polypeptide chain. C9 is a part of the membrane attack complex (MAC), an important component of the immune system. The MAC forms upon complement system activation by invading pathogenic bacteria and consists of the four major complement proteins: C5b, C6, C7 and C8. These complement proteins bind to the outer surface of the plasma membrane of the invading cell. C9 binds to the membrane associated C5b-8 protein, which leads to the circular polymerization of 12-18 C9 molecules. These polymerized C9 molecules form a ring structure in the membrane. Molecules can then diffuse freely through this transmembrane channel, causing cell lysis and destruction of the invading bacterial cell.
VE:
1 * 100 µl
Artikel-Nr:
(BRND81248)
Lieferant:
Brand
Hersteller-Artikelnummer::
81248
Lokale Artikelnummer::
BRND81248
Beschreibung:
Braunglas Borosilikatglas 5,4
VE:
1 * 1 ST
Artikel-Nr:
(ROCK611-1622-0500)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
611-1622-0500
Lokale Artikelnummer::
ROCK611-1622-0500
Beschreibung:
This product has been assayed against 1.0 µg of Rabbit IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
VE:
1 * 500 µG
Artikel-Nr:
(BOSSBS-8346R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8346R-CY7
Lokale Artikelnummer::
BOSSBS-8346R-CY7
Beschreibung:
FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
VE:
1 * 100 µl
Artikel-Nr:
(EHERC12194000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C12194000
Lokale Artikelnummer::
EHERC12194000
Beschreibung:
trans-1,2-Diaminocyclohexan-N,N,N',N'-tetraessigsäure Monohydrat
VE:
1 * 0,25 g
Artikel-Nr:
(FLUO015748-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
015748-1G
Lokale Artikelnummer::
FLUO015748-1G
Beschreibung:
2,7-Dimethylimidazo[1,2-a]pyridin-3-carbaldehyd
VE:
1 * 1 g
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Artikel-Nr:
(BOSSBS-12057R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12057R
Lokale Artikelnummer::
BOSSBS-12057R
Beschreibung:
eIF3K (Eukaryotic translation initiation factor 3 subunit K, Muscle-specific gene M9 protein) is a widely expressed translation initiation factor that belongs to the eIF3 subunit K family. Translation initiation factor 3 (eIF3) is a multisubunit complex containing at least 12 subunits. eIF3 binds to the 40S ribosomal subunit, promotes the binding of methionyl-tRNAi and mRNA, and interacts with several other initiation factors to form the 40S initiation complex. eIF3K is the smallest subunit of eIF3 and it interacts with several other subunits of eIF3 and the 40S ribosomal subunit. eIF3K is conserved among high eukaryotes, including mammals, insects, and plants, and it is ubiquitously expressed in human tissues. eIF3K is distributed both in nucleus and cytoplasm and colocalizes with cyclin D3, a regulatory subunit of cyclin-dependent kinase 4 (Cdk4).
VE:
1 * 100 µl
Lieferant:
BACHEM BIOCHEMICA
Beschreibung:
N-Dodecanoyl-N-methyl-D-glucamin (MEGA-12)
Lieferant:
Thermo Scientific
Beschreibung:
Bromthymolblau Natriumsalz, wasserlöslich, rein Indikator
Preis auf Anfrage
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