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Ethyldiethoxyacetat
Lieferant:
Merck
Beschreibung:
(1S)-(-)-Borneol zur Synthese, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-15317R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15317R
Lokale Artikelnummer::
BOSSBS-15317R
Beschreibung:
C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15313R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R-HRP
Lokale Artikelnummer::
BOSSBS-15313R-HRP
Beschreibung:
C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15347R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15347R
Lokale Artikelnummer::
BOSSBS-15347R
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf91 gene product has been provisionally designated C9orf91 pending further characterization. There are three isoforms of C9orf91 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15338R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15338R
Lokale Artikelnummer::
BOSSBS-15338R
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf68 gene product has been provisionally designated C9orf68 pending further characterization. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
These overalls are made from a highly breathable anti-static SMS fabric which utilises the latest developments in micro-fibre technology to ensure good filtration efficiency.
Lieferant:
DICKSON
Beschreibung:
Diagramm für Schreiber, C320, +22...+68 °F
Lieferant:
MACHEREY-NAGEL
Beschreibung:
CHROMABOND® C18 ist eine octadecylmodifizierte Silicaphase für SPE.
Artikel-Nr:
(233-0004)
Lieferant:
MURRAY S
Hersteller-Artikelnummer::
D021/G3
Lokale Artikelnummer::
MURRD021/G3
Beschreibung:
These scalpels with light pattern are completely made from stainless steel.
VE:
1 * 1 ST
Artikel-Nr:
(KART1360)
Lieferant:
KARTELL
Hersteller-Artikelnummer::
1360
Lokale Artikelnummer::
KART1360
Beschreibung:
Zwei PTFE-Filter, 0,20–45 µm, Für: Seropet
VE:
1 * 1 ST
Lieferant:
Portwest Clothing
Beschreibung:
High performance upper design with 3D mesh lining which provides maximum comfort and breathability. This trend setting safety footwear has been constructed with a dual density PU/PU outsole, providing superior grip and energy absorption. Designed with a cushioned footbed reducing foot fatigue.
Artikel-Nr:
(BOSSBS-12157R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12157R-A555
Lokale Artikelnummer::
BOSSBS-12157R-A555
Beschreibung:
The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a motif of eight cysteines. This gene product can exist either as a homodimer (PDGF-BB) or as a heterodimer with the platelet-derived growth factor alpha polypeptide (PDGF-AB), where the dimers are connected by disulfide bonds. Mutations in this gene are associated with meningioma. Reciprocal translocations between chromosomes 22 and 7, at sites where this gene and that for COL1A1 are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans resulting from unregulated expression of growth factor. Two alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Oct 2008].
VE:
1 * 100 µl
Lieferant:
ATLAS - the shoe company
Beschreibung:
Leichte, metallfreie ESD-Schuhe aus atmungsaktivem Obermaterial, leichten Innenmaterialien und einer MPU® Light Laufsohle (3,5 mm Profil, öl-, säure-, kraftstoffbeständig; antistatisch).
Artikel-Nr:
(BOSSBS-9494R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9494R-FITC
Lokale Artikelnummer::
BOSSBS-9494R-FITC
Beschreibung:
C9orf114 is a 376 amino acid protein encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9490R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9490R-A750
Lokale Artikelnummer::
BOSSBS-9490R-A750
Beschreibung:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukaemias. The KIAA1529 gene product has been provisionally designated KIAA1529 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12499R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12499R-A750
Lokale Artikelnummer::
BOSSBS-12499R-A750
Beschreibung:
The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-IV (apolipoprotein L-IV), also known as APOL4, is a 351 amino acid protein that exists as multiple alternatively spliced isoforms, one of which is secreted. Expressed in spleen, placenta, spinal cord, uterus, testis and trachea, apoL-IV is thought to play a role in lipid exchange and transport throughout the body and may be involved in reverse cholesterol transport, specifically from peripheral cells to the liver. Overexpression of apoL-IV is associated with schizophrenia, suggesting that apoL-IV may play a role in the pathogenesis of neural 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.
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