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1,4-Dibromo-3,5-difluorobenzene
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1,4-Dibromo-3,5-difluorobenzene
Artikel-Nr:
(BOSSBS-9678R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9678R-CY3
Lokale Artikelnummer::
BOSSBS-9678R-CY3
Beschreibung:
C19orf21 is a 679 amino acid protein that is 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-9681R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9681R-A680
Lokale Artikelnummer::
BOSSBS-9681R-A680
Beschreibung:
C19orf45 is a 505 amino acid protein that is 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 recognised 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 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 BCL3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0264R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0264R-HRP
Lokale Artikelnummer::
BOSSBS-0264R-HRP
Beschreibung:
Cytochrome c oxidase, the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of three catalytic subunits encoded by mitochondrial genes, and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, while the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 2 (liver isoform) of subunit VIIa, with this polypeptide being present in both muscle and non-muscle tissues. In addition to polypeptide 2, subunit VIIa includes polypeptide 1(muscle isoform), which is present only in muscle tissues, and a related protein, which is present in all tissues. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4 and 14. [provided by RefSeq, Oct 2009].
VE:
1 * 100 µl
Artikel-Nr:
(1074073.)
Lieferant:
USP
Hersteller-Artikelnummer::
1074073
Lokale Artikelnummer::
USPH1074073
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 20 mg
Artikel-Nr:
(1642824.)
Lieferant:
USP
Hersteller-Artikelnummer::
1642824
Lokale Artikelnummer::
USPH1642824
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 15 mg
Lieferant:
GRANT INSTRUMENTS
Beschreibung:
Diese digitalen Wasserbäder ohne Rührfunktion sind mit Kapazitäten von 5 bis 26 Litern verfügbar. Alle Einheiten haben Edelstahltanks und langlebige lackierte Stahlgehäuse, bieten schnelle Aufheizzeiten, eine gute Temperaturkontrolle, eine Verriegelung an der Vorderseite, benutzerfreundliche Bedienelemente und eine helle, übersichtliche Anzeige. Alle Bäder sind mit Heizmattentechnologie für einen optimalen Arbeitsbereich ausgestattet - ohne Heizelement im Tank sind sie leichter zu reinigen. Die größeren Modelle ab 12 Liter aufwärts verfügen über einen praktischen Ablaufhahn an der Vorderseite des Bads. Das Sortiment ist ideal für den Einsatz in Bildung und Ausbildung sowie in industriellen Anwendungen wie der Produkt- und Materialprüfung.
Artikel-Nr:
(COBBOS-1034-100G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
OS-1034-100G
Lokale Artikelnummer::
COBBOS-1034-100G
Beschreibung:
1-Brom-3,5-di-tert-butylbenzol
VE:
1 * 100 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11955R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11955R-A350
Lokale Artikelnummer::
BOSSBS-11955R-A350
Beschreibung:
SLITRK family proteins are integral membrane proteins that have a C-terminal domain that is partially similar to TRK neurotrophin receptor proteins and two leucine-rich repeat (LRR) domains that are similar to those of SLIT proteins. SLITRK2 (SLIT and NTRK-like protein 2) is a 845 amino acid single-pass type I membrane protein that contains 14 LRR (leucine-rich) repeats and is expressed in neural tissues, with highest levels found in adult cerebral cortex. Overexpression of SLITRK2 leads to inhibition of unipolar neurites in cultured cells, suggesting that it suppresses neurite outgrowth. Inhibitory activity of SLITRK2 is localized to its C-terminal intracellular domain and without this region the protein induces neurite outgrowth. Variants in the gene encoding SLITRK2 may contribute to the development of bipolar disorder, autism spectrum disorder and schizophrenia. There are two isoforms of SLITRK2 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11955R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11955R-A555
Lokale Artikelnummer::
BOSSBS-11955R-A555
Beschreibung:
SLITRK family proteins are integral membrane proteins that have a C-terminal domain that is partially similar to TRK neurotrophin receptor proteins and two leucine-rich repeat (LRR) domains that are similar to those of SLIT proteins. SLITRK2 (SLIT and NTRK-like protein 2) is a 845 amino acid single-pass type I membrane protein that contains 14 LRR (leucine-rich) repeats and is expressed in neural tissues, with highest levels found in adult cerebral cortex. Overexpression of SLITRK2 leads to inhibition of unipolar neurites in cultured cells, suggesting that it suppresses neurite outgrowth. Inhibitory activity of SLITRK2 is localized to its C-terminal intracellular domain and without this region the protein induces neurite outgrowth. Variants in the gene encoding SLITRK2 may contribute to the development of bipolar disorder, autism spectrum disorder and schizophrenia. There are two isoforms of SLITRK2 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11955R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11955R-A488
Lokale Artikelnummer::
BOSSBS-11955R-A488
Beschreibung:
SLITRK family proteins are integral membrane proteins that have a C-terminal domain that is partially similar to TRK neurotrophin receptor proteins and two leucine-rich repeat (LRR) domains that are similar to those of SLIT proteins. SLITRK2 (SLIT and NTRK-like protein 2) is a 845 amino acid single-pass type I membrane protein that contains 14 LRR (leucine-rich) repeats and is expressed in neural tissues, with highest levels found in adult cerebral cortex. Overexpression of SLITRK2 leads to inhibition of unipolar neurites in cultured cells, suggesting that it suppresses neurite outgrowth. Inhibitory activity of SLITRK2 is localized to its C-terminal intracellular domain and without this region the protein induces neurite outgrowth. Variants in the gene encoding SLITRK2 may contribute to the development of bipolar disorder, autism spectrum disorder and schizophrenia. There are two isoforms of SLITRK2 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11480R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11480R-HRP
Lokale Artikelnummer::
BOSSBS-11480R-HRP
Beschreibung:
Semaphorins are a family of cell surface and secreted proteins involved in neural development that are conserved from insects to humans. Members of this family are approximately 750 amino acids in length (including signal sequences) and are defined by a conserved extracellular “semaphorin†domain of approximately 500 amino acids containing 14-16 cysteines, blocks of conserved sequences and no obvious repeats. The transmembrane semaphorins are characterized by an additional 80 amino acid transmembrane domain and an 80-110 amino acid cytoplasmic domain. Secreted and cell-bound semaphorins chemically attract and repel the growth of neural axons, guiding the development of intricate networks of neural tissue. SEMA3E is a secreted semaphorin with 775 amino acids. Mutations in the SEMA3E gene are associated with CHARGE syndrome, a disorder characterized by cranial nerve dysfunction, coloboma of the eye, choanal atresia, inner and external ear abnormalities, cardiac anomalies, genitourinary abnormalities, and growth retardation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9677R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9677R-HRP
Lokale Artikelnummer::
BOSSBS-9677R-HRP
Beschreibung:
C19orf18 is a 215 amino acid single-pass type I membrane protein that is 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:
(USBI150343)
Lieferant:
US Biological
Hersteller-Artikelnummer::
150343
Lokale Artikelnummer::
USBI150343
Beschreibung:
Anti-DUSP14 Goat Polyclonal Antibody
VE:
1 * 100 µG
Artikel-Nr:
(ABNOPAB9617)
Lieferant:
Abnova
Hersteller-Artikelnummer::
PAB9617
Lokale Artikelnummer::
ABNOPAB9617
Beschreibung:
Anti-14-3-3 Rabbit Polyclonal Antibody
VE:
1 * 100 µl
Artikel-Nr:
(USBI032174)
Lieferant:
US Biological
Hersteller-Artikelnummer::
032174
Lokale Artikelnummer::
USBI032174
Beschreibung:
Anti-ATG14 Rabbit Polyclonal Antibody
VE:
1 * 200 µl
Artikel-Nr:
(BOSSBS-8409R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-A555
Lokale Artikelnummer::
BOSSBS-8409R-A555
Beschreibung:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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.
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