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Trisodium+naphthalene-1,3,5-trisulphonate
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Trisodium+naphthalene-1,3,5-trisulphonate
Artikel-Nr:
(BOSSBS-15312R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15312R-A350
Lokale Artikelnummer::
BOSSBS-15312R-A350
Beschreibung:
C9orf135 (chromosome 9 open reading frame 135) is a 229 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 9q21.11. 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 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-11048R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11048R-FITC
Lokale Artikelnummer::
BOSSBS-11048R-FITC
Beschreibung:
Copper is an essential micronutrient used as a co-factor for several essential enzymes in all living organisms. Due to the high toxicity of copper, its metabolism is tightly regulated and defects in this regulation can cause Menkes (deficiency) or Wilson (accumulation) disease in various tissue. CUTC (cutC copper transporter homolog (E. coli)), also known as CGI-32, is a 273 amino acid protein belonging to the cutC family. CUTC is involved in copper homeostasis and is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. Other chromosome 10 associated disorders include Cockayne syndrome, tetrahydrobiopterin deficiency and trisomy 10.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9659R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A680
Lokale Artikelnummer::
BOSSBS-9659R-A680
Beschreibung:
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. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterisation.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Trimesinsäuretrimethylester, Sigma-Aldrich®
Artikel-Nr:
(MOLE14579217-1KG)
Lieferant:
Molekula
Hersteller-Artikelnummer::
14579217-1KG
Lokale Artikelnummer::
MOLE14579217-1KG
Beschreibung:
Dichlor-1,3,5-triazintrion Natriumsalz Dihydrat
VE:
1 * 1 kg
 This is a MarketSource item. Additional charges may apply
Lieferant:
Lovibond Tintometer
Beschreibung:
Cyanursäure
Artikel-Nr:
(506172-10MG)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
506172-10MG
Lokale Artikelnummer::
CALB506172-10MG
Beschreibung:
p38 MAP kinase inhibitor X, BIRB 796, is a cell-permeable, highly potent, slow binding, high affinity inhibitor of p38a (IC50 = 8 and 97 nM with or without 2 h preincubation).
VE:
1 * 10 mg
Lieferant:
RUBBERMAID
Beschreibung:
Strapazierfähige und attraktive Aufbewahrungs- und Transportwagen für Front- und Back-of-House-Anwendungen.
Artikel-Nr:
(MOLE35283847-5G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
35283847-5G
Lokale Artikelnummer::
MOLE35283847-5G
Beschreibung:
5-Azacytosin
VE:
1 * 5 g
This is a MarketSource item. Additional charges may apply
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
Artikel-Nr:
(BOSSBS-8409R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8409R-A750
Lokale Artikelnummer::
BOSSBS-8409R-A750
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
Artikel-Nr:
(BOSSBS-6384R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6384R-A488
Lokale Artikelnummer::
BOSSBS-6384R-A488
Beschreibung:
C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9720R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9720R-CY7
Lokale Artikelnummer::
BOSSBS-9720R-CY7
Beschreibung:
C10orf27, also known as spatial, is a 351 amino acid cytoplasmic protein belonging to the spatial family. C10orf27 is suggested to play a role in spermatid differentiation. Existing as two alternatively spliced isoforms, C10orf27 is widely expressed in multiple tissues, including brain, thymus and testis. C10orf27 may be associated with multiple sclerosis (MS) susceptibility and pathogenesis. MS is an inflammatory disease that causes gradual destruction of myelin in the central nervous system. C10orf27 is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(EHERC17664000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C17664000
Lokale Artikelnummer::
EHERC17664000
Beschreibung:
2,4,6-Tribromanisol
VE:
1 * 0,1 g
Lieferant:
BURKLE
Beschreibung:
Nippel, Außengewinde, PP, 12,7 nominale Breite 13,5 mm, PP, Gewinde: 12,7 mm
Artikel-Nr:
(BOSSBS-8215R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8215R-CY7
Lokale Artikelnummer::
BOSSBS-8215R-CY7
Beschreibung:
FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
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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