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2,2-Difluoroethyl+3-fluoropropyl+carbonate
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2,2-Difluoroethyl+3-fluoropropyl+carbonate
Artikel-Nr:
(EHERL20015300IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20015300IO
Lokale Artikelnummer::
EHERL20015300IO
Beschreibung:
Organic Standard, 2,2',4,4',5,5'-Hexachlorbiphenyl (PCB Nr. 153) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(EHERL20012800IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20012800IO
Lokale Artikelnummer::
EHERL20012800IO
Beschreibung:
Organic Standard, 2,2',3,3',4,4'-Hexachlorbiphenyl (PCB Nr. 128) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(EHERL20018100IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20018100IO
Lokale Artikelnummer::
EHERL20018100IO
Beschreibung:
Organic Standard, 2,2',3,4,4',5,6-Heptachlorbiphenyl (PCB Nr. 181) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Lieferant:
Biotium
Beschreibung:
This MAb reacts with a protein of 22 kDa, identified as beta subunit of HCG. It does not cross react with the alpha subunit. HCG is a glycoprotein, which is secreted in large quantities by normal trophoblasts. It is present only in trace amounts in non-pregnant urine and sera but rises sharply during pregnancy. HCG is composed of two non-identical, non-covalently linked polypeptide chains designated as the alpha and beta subunits. The alpha subunit is identical to that of thyroid stimulating hormone (TSH), follicle stimulating hormone (FSH), and luteinizing hormone (LH). hCG MAb detects cells and tumors of trophoblastic origin such as choriocarcinoma. Large cell carcinoma and adenocarcinoma of the lung demonstrate anti-hCG positivity in 90% and 60% of cases respectively. 20% of lung squamous cell carcinomas are positive. hCG expression by non-trophoblastic tumors may indicate aggressive behavior.
Artikel-Nr:
(BOSSBS-10180R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10180R-A750
Lokale Artikelnummer::
BOSSBS-10180R-A750
Beschreibung:
Capsid protein self-assembles to form an icosahedral capsid with a T=1 symmetry, about 22 nm in diameter, and consisting of 60 copies of three size variants of the capsid protein VP1, VP2 and VP3 which differ in their N-terminus. The capsid encapsulates the genomic ssDNA. Binds to host cell heparan sulfate and uses host ITGA5-ITGB1 as coreceptor on the cell surface to provide virion attachment to target cell. This attachment induces virion internalisation predominantly through clathrin-dependent endocytosis. Binding to the host receptor also induces capsid rearrangements leading to surface exposure of VP1 N-terminus, specifically its phospholipase A2-like region and putative nuclear localisation signal(s). VP1 N-terminus might serve as a lipolytic enzyme to breach the endosomal membrane during entry into host cell and might contribute to virus transport to the nucleus.
VE:
1 * 100 µl
Lieferant:
ZEISS
Beschreibung:
Accessory for microscopes, Für: Axiostar, Okular PL, 10× /22 Br. foc.
Artikel-Nr:
(818-0132)
Lieferant:
Texwipe
Hersteller-Artikelnummer::
TX5811
Lokale Artikelnummer::
TEXWTX5811
Beschreibung:
TexWrite® 22, latex-saturated cellulose cleanroom documentation sheets without organic fillers.
VE:
1 * 2.500 ST
Artikel-Nr:
(BOSSBS-15318R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-CY5
Lokale Artikelnummer::
BOSSBS-15318R-CY5
Beschreibung:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 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-15318R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-FITC
Lokale Artikelnummer::
BOSSBS-15318R-FITC
Beschreibung:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 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-15314R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R
Lokale Artikelnummer::
BOSSBS-15314R
Beschreibung:
C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic 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
Lieferant:
Sigma-Aldrich
Beschreibung:
4,4'-Isopropylidendiphenol, Sigma-Aldrich®
Artikel-Nr:
(253300-10)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
253300-10
Lokale Artikelnummer::
CALB253300-10
Beschreibung:
Deltamethrin is a synthetic type II pyrethroid that acts as a potent inhibitor of calcineurin (protein phosphatase 2B; IC50 = 100 pM). Also have varied effects on ion channels. Causes an increase in neurotransmitter release at synapses, and increases intrasynaptosomal Ca<sup>2+</sup> levels.
VE:
1 * 10 mg
Artikel-Nr:
(BRND473500)
Lieferant:
Brand
Hersteller-Artikelnummer::
473500
Lokale Artikelnummer::
BRND473500
Beschreibung:
Färbeplatte, Natronkalkglas, Klar, B×T×H: 130×100×6 mm, Anzahl Wells: 12, Lochgröße: Ø: 20 - 22 mm
VE:
1 * 1 ST
Artikel-Nr:
(MOLE47008781-1G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
47008781-1G
Lokale Artikelnummer::
MOLE47008781-1G
Beschreibung:
(R)-(+)-1,1'-Bi-2-naphthol
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
FLUOROCHEM
Beschreibung:
2-Benzyloxyphenylacetonitril
Artikel-Nr:
(EHERL20019400IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20019400IO
Lokale Artikelnummer::
EHERL20019400IO
Beschreibung:
Organic Standard, 2,2',3,3',4,4',5,5'-Octachlorbiphenyl (PCB Nr. 194) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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