5-Chloro-1,6-naphthyridine
Artikel-Nr:
(BOSSBS-15342R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15342R-A350
Lokale Artikelnummer::
BOSSBS-15342R-A350
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 leukemias. The C9orf78 gene product has been provisionally designated C9orf78 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15328R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15328R-A488
Lokale Artikelnummer::
BOSSBS-15328R-A488
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 leukemias. The C9orf40 gene product has been provisionally designated C9orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15337R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15337R-A680
Lokale Artikelnummer::
BOSSBS-15337R-A680
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 leukemias. The C9orf66 gene product has been provisionally designated C9orf66 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15328R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15328R-A555
Lokale Artikelnummer::
BOSSBS-15328R-A555
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 leukemias. The C9orf40 gene product has been provisionally designated C9orf40 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Pivalaldehyd (Trimethylacetaldehyd)
Lieferant:
Sigma-Aldrich
Beschreibung:
Diethylenglycol, Sigma-Aldrich®
Artikel-Nr:
(PROOCIL-PCB-19-CS)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-19-CS
Lokale Artikelnummer::
PROOCIL-PCB-19-CS
Beschreibung:
Organic Standard, 2,2',6-Trichlorbiphenyl (PCB Nr. 19) 100 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 1,2 mL
Artikel-Nr:
(PROOCIL-PCB-17)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-17
Lokale Artikelnummer::
PROOCIL-PCB-17
Beschreibung:
Organic Standard, 2,2',4-Trichlorbiphenyl (PCB Nr. 17) 35 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 1 mL
Artikel-Nr:
(PROOCIL-PCB-19)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-19
Lokale Artikelnummer::
PROOCIL-PCB-19
Beschreibung:
Organic Standard, 2,2',6-Trichlorbiphenyl (PCB Nr. 19) 35 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 1 mL
Artikel-Nr:
(PROOCIL-PCB-18-CS)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-18-CS
Lokale Artikelnummer::
PROOCIL-PCB-18-CS
Beschreibung:
Organic Standard, 2,2',5-Trichlorbiphenyl (PCB Nr. 18) 100 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 1,2 mL
Artikel-Nr:
(SIMPT110-10)
Lieferant:
Simport Scientific
Hersteller-Artikelnummer::
T110-10
Lokale Artikelnummer::
SIMPT110-10
Beschreibung:
PP. This 2,2 ml well capacity (2,1 ml when capped) plate is used mainly for compound storage and enzyme assays.
VE:
1 * 24 ST
Artikel-Nr:
(BOSSBS-9656R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9656R-A647
Lokale Artikelnummer::
BOSSBS-9656R-A647
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 FAM78A gene product has been provisionally designated FAM78A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(EHERL20000400IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20000400IO
Lokale Artikelnummer::
EHERL20000400IO
Beschreibung:
Organic Standard, 2,2'-Dichlorbiphenyl (PCB Nr. 4) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Lieferant:
Agilent
Beschreibung:
Replacement needle 100 μl, 22s G, 51 mm, tip 3
Artikel-Nr:
(PRSI7593)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
7593
Lokale Artikelnummer::
PRSI7593
Beschreibung:
Interleukin-22 (IL-22) is a cytokine important for the modulation of tissue responses during inflammation. Unlike the distantly related IL-10, IL-22 does not inhibit the production of proinflammatory cytokines in monocytes in response to LPS, but it has some inhibitory effects on IL-4 production from Th2 T cells. IL-22 is expressed by both the adaptive arm of the immune system such as CD4 T cell subsets including Th17 cells, as well as by innate lymphocytes such as NK and LTi-like cells. IL-22 is highly expressed in several chronic inflammatory conditions, and studies suggest that IL-22 plays both inflammatory and protective roles.
VE:
1 * 100 µG
Artikel-Nr:
(PRSI24-315)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
24-315
Lokale Artikelnummer::
PRSI24-315
Beschreibung:
Anti-GSTP1 Recombinant Antibody [Clone: SAIC-22D-22]
VE:
1 * 0,2 mg
New Product
Preis auf Anfrage
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