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3,3-Dimethoxypropiononitril
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3,3-Dimethoxypropiononitril
Artikel-Nr:
(SIAL697958-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
697958-1G
Lokale Artikelnummer::
SIAL697958-1G
Beschreibung:
5,5-Dimethylacetylaceton, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(HONC34661-2.5L)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
34661-2.5L
Lokale Artikelnummer::
HONC34661-2.5L
Beschreibung:
Indigocarmin-Lösung für PANPEHA-Indikatorpapier, Riedel-de Haën™
VE:
1 * 2,5 L
Artikel-Nr:
(36893-2ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
36893-2ML
Lokale Artikelnummer::
SUPL36893-2ML
Beschreibung:
Organic Standard, trans-Permethrin 10 µg/ml in Cyclohexan, Packung: Glasflasche
VE:
1 * 2 mL
Lieferant:
MP Biomedicals
Beschreibung:
1,3-Propane Sultone was used as quaternisation agent to transit the PDMAEMA into poly(zwitterions) through surface reaction by treating membranes under a mild condition.
Lieferant:
Brand
Beschreibung:
Borosilikatglas 3.3, klar.
Artikel-Nr:
(BOCH3645)
Lieferant:
BOCHEM
Hersteller-Artikelnummer::
3645
Lokale Artikelnummer::
BOCH3645
Beschreibung:
Stainless steel 18/10.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9748R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9748R-A350
Lokale Artikelnummer::
BOSSBS-9748R-A350
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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:
(637-0192)
Lieferant:
ELTRA
Hersteller-Artikelnummer::
90155
Lokale Artikelnummer::
ELTA90155
Beschreibung:
Accessories for elemental analyser, Verbrennungsschalen, Keramik, wieder verwendbar; 59×22×14 mm, für CS-530
VE:
1 * 500 ST
Artikel-Nr:
(EHERC15144200)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C15144200
Lokale Artikelnummer::
EHERC15144200
Beschreibung:
2-(Methylthio)benzothiazol
VE:
1 * 0,1 g
Artikel-Nr:
(BOSSBS-12330R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12330R-A750
Lokale Artikelnummer::
BOSSBS-12330R-A750
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterised by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. Staf-50 (50 kDa-stimulated trans-acting factor), also known as TRIM22 (tripartite motif-containing 22), RNF94 or GPSTAF50, is a 498 amino acid cytoplasmic protein that belongs to the TRIM family and, characteristic of TRIM family members, contains one RING-type zinc finger, one B box-type zinc finger and one SPRY domain. Induced by IFN-å and IFN-, Staf-50 is strongly expressed in ovary, spleen, thymus and peripheral blood leukocytes where it is thought to mediate the antiviral effects of IFN proteins. Additionally, Staf-50 is present in leukemic cells, suggesting a role in cancer formation and metastasis. Staf-50 exists as two alternatively spliced isoforms which are encoded by a gene that maps to human chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9492R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9492R
Lokale Artikelnummer::
BOSSBS-9492R
Beschreibung:
C9orf4 is a 344 amino acid single-pass membrane protein that is primarily expressed in adult and fetal brain and is weakly expressed in spinal cord, adult ovary and medulla. C9orf4 contains one DOMON domain, a predominantly β-sheet domain that is thought to aide in extracellular adhesion. The gene encoding C9orf4 maps to human chromosome 9, which 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.
VE:
1 * 100 µl
Lieferant:
GLASWARENFABRIK KARL HECHT
Beschreibung:
Enghalsflaschen, klares oder braunes Glas, mit schwarzer PP Schraubkappe Exzellent zur Probenentnahme, Lagerung und zum Transport von Flüssigkeiten.
Artikel-Nr:
(BOSSBS-8594R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R
Lokale Artikelnummer::
BOSSBS-8594R
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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-8594R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-A647
Lokale Artikelnummer::
BOSSBS-8594R-A647
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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-8594R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-CY3
Lokale Artikelnummer::
BOSSBS-8594R-CY3
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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-8594R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-CY5
Lokale Artikelnummer::
BOSSBS-8594R-CY5
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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
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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