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4,4,4-Trifluoro-3-(trifluoromethyl)butanoic+acid
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4,4,4-Trifluoro-3-(trifluoromethyl)butanoic+acid
Artikel-Nr:
(PRSI4793P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
4793P
Lokale Artikelnummer::
PRSI4793P
Beschreibung:
ACVR1B peptide is used for blocking the activity of ACVR1B antibody.
VE:
1 * 50 µG
Artikel-Nr:
(USBI037523)
Lieferant:
US Biological
Hersteller-Artikelnummer::
037523
Lokale Artikelnummer::
USBI037523
Beschreibung:
Anti-KLF14 Rabbit Polyclonal Antibody
VE:
1 * 200 µl
Lieferant:
Thermo Scientific
Beschreibung:
HEPES Natriumsalz 99%
Lieferant:
EPPENDORF
Beschreibung:
Adapter für Rotoren, für 24 Röhrchen 14 ml, für Rotor S-4×Universal-Large, 2 Stück
Artikel-Nr:
(PRSI3227P)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
3227P
Lokale Artikelnummer::
PRSI3227P
Beschreibung:
ACE2 peptide is used for blocking the activity of ACE2 antibody.
VE:
1 * 50 µG
Lieferant:
DWK Life Sciences
Beschreibung:
Klemmring, KECK™, für Adapter KA, für Gewinde RD 14, rot
Lieferant:
IKA
Beschreibung:
Reactor lid for the EasySyn reactor system, openings: 3×NS 29/32, 1×NS 14/23
Artikel-Nr:
(PRSI91-464)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
91-464
Lokale Artikelnummer::
PRSI91-464
Beschreibung:
beta -1,4-galactosyltransferase 4 (B4GALT4) is a single-pass type II membrane protein that belongs to the Glycosyltransferase 7 family. B4GALT4 consist of the following 2 domains: N-Acetyllactosamine Synthase and beta -N-Acetylglucosaminyl-Glycolipid beta -1,4-Galactosyltransferase. B4GALT4 is highly expressed in the heart, placenta, kidney, and pancreas; it is lowly expressed in the brain, colon, lung, muscle, ovary, testis, and uterus. B4GALT4 function is responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids.
VE:
1 * 50 µG
Artikel-Nr:
(EHERL20421400IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20421400IO
Lokale Artikelnummer::
EHERL20421400IO
Beschreibung:
Organic Standard, 1,4-Dichlornaphthalin 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(BOSSBS-9740R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9740R-A555
Lokale Artikelnummer::
BOSSBS-9740R-A555
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-6073R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6073R-A680
Lokale Artikelnummer::
BOSSBS-6073R-A680
Beschreibung:
Sodium-dependent lysophosphatidylcholine (LPC) symporter, which plays an essential role for blood-brain barrier formation and function. Specifically expressed in endothelium of the blood-brain barrier of micro-vessels and transports LPC into the brain. Transport of LPC is essential because it constitutes the major mechanism by which docosahexaenoic acid (DHA), an omega-3 fatty acid that is essential for normal brain growth and cognitive function, enters the brain. Transports LPC carrying long-chain fatty acids such LPC oleate and LPC palmitate with a minimum acyl chain length of 14 carbons. Does not transport docosahexaenoic acid in unesterified fatty acid. Specifically required for blood-brain barrier formation and function, probably by mediating lipid transport. Not required for central nervous system vascular morphogenesis (By similarity). Acts as a transporter for tunicamycin, an inhibitor of asparagine-linked glycosylation. In placenta, acts as a receptor for ERVFRD-1/syncytin-2 and is required for trophoblast fusion (PubMed:18988732).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13605R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13605R-A488
Lokale Artikelnummer::
BOSSBS-13605R-A488
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
Artikel-Nr:
(BOSSBS-9684R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9684R-HRP
Lokale Artikelnummer::
BOSSBS-9684R-HRP
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-13605R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13605R-A647
Lokale Artikelnummer::
BOSSBS-13605R-A647
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
Artikel-Nr:
(BOSSBS-3655R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3655R-A750
Lokale Artikelnummer::
BOSSBS-3655R-A750
Beschreibung:
This gene is a member of the kernel lipocalin superfamily whose members share relatively low sequence similarity but have highly conserved exon/intron structure and three-dimensional protein folding. Most lipocalins are clustered on the long arm of chromosome 9. The encoded glycoprotein has been previously referred to as pregnancy-associated endometrial alpha-2-globulin, placental protein 14, and glycodelin, but has been officially named progestagen-associated endometrial protein. Three distinct forms, with identical protein backbones but different glycosylation profiles, are found in amniotic fluid, follicular fluid and seminal plasma of the reproductive system. These glycoproteins have distinct and essential roles in regulating a uterine environment suitable for pregnancy and in the timing and occurrence of the appropriate sequence of events in the fertilization process. A number of alternatively spliced transcript variants have been observed at this locus, but the full-length nature of only two, each encoding the same protein, has been determined.
VE:
1 * 100 µl
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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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