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chromolith+WP+300
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chromolith+WP+300
Fournisseur:
TCI
Description:
(±)-Acide 3-hydroxybutyrique ≥80.0% (par analyse titrimétrique) (contains Polymolecular esterification product)
Numéro de catalogue:
(710-0743)
Fournisseur:
DOEHLER GROUP
Description:
Poudre pour la fabrication de bouillon NBB®-Broth et de gélose NBB®-Agar, destinés à la détection des bactéries contaminant la bière dans des échantillons de bière filtrée, des échantillons d'eau, des échantillons de levures et des échantillons sur membrane et écouvillon. Sous sa marque NBB®, Döhler propose des milieux de culture innovants pour la détection rapide et fiable des microorganismes contaminant les boissons (par exemple, les bactéries Lactobacillus, Pectinatus et Megasphaera), et ce dans tous les échantillons provenant de brasseries, ainsi que pour l'industrie du vin. La poudre NBB®-Powder (NBB®-P) se dissout dans la bière et adapte la sélectivité des milieux NBB®-Media à la spécificité des produits. Les milieux de culture NBB® peuvent être utilisés pour la détection des éléments suivants :
UOM:
1 * 300 g
Fournisseur:
Biotium
Description:
In Western blotting, this antibody reacts with two bands of ~MW of 210 kDa and 300 kDa, identified as two isoforms of Tenascin C. Specificity of this MAb is validated by sequential immunoprecipitation with a PAb against Tenascin C. Tenascin C is a multifunctional, disulfide-linkedhexameric extracellular matrix glycoprotein expressed in association with mesenchymal epithelial interactions during development and in the neo-vasculature and stroma of undifferentiated tumors. In adults, it is restricted to certain epithelial-stromal interfaces and increases markedly in hyper-proliferative diseases and in stroma of many neoplasms, including gliomas, breast, squamous and lung carcinomas.
Fournisseur:
Biotium
Description:
In Western blotting, this antibody reacts with two bands of ~MW of 210 kDa and 300 kDa, identified as two isoforms of Tenascin C. Specificity of this MAb is validated by sequential immunoprecipitation with a PAb against Tenascin C. Tenascin C is a multifunctional, disulfide-linkedhexameric extracellular matrix glycoprotein expressed in association with mesenchymal epithelial interactions during development and in the neo-vasculature and stroma of undifferentiated tumors. In adults, it is restricted to certain epithelial-stromal interfaces and increases markedly in hyper-proliferative diseases and in stroma of many neoplasms, including gliomas, breast, squamous and lung carcinomas.
Numéro de catalogue:
(BOSSBS-5339R-A680)
Fournisseur:
Bioss
Description:
KAT3B/p300 is a transcriptional adapter protein (300 kDa)which is characterised by three cysteine and histidine rich regions and its C-terminus specifically binds the adenovirus E1A protein. KAT3B and associated proteins are components of TATA-binding protein (TBP)complexes. Protein kinase A mediated CREB phosphorylation results in the binding of CREB to a 265 kDa nuclear protein designated KAT3A/CBP(for CREB-binding protein). KAT3B and KAT3A are homologous to each other.
UOM:
1 * 100 µl
Fournisseur:
ANSELL HEALTH CARE
Description:
Ces gants en nitrile offrent une grande résistance aux produits chimiques, et une résistance à la perforation trois fois supérieure à celle des gants en latex classiques.
Numéro de catalogue:
(BOSSBS-9676R-FITC)
Fournisseur:
Bioss
Description:
MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9676R-A488)
Fournisseur:
Bioss
Description:
MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
UOM:
1 * 100 µl
Numéro de catalogue:
(BTIUBNUM0392-50)
Fournisseur:
Biotium
Description:
In Western blotting, this antibody reacts with two bands of ~MW of 210 kDa and 300 kDa, identified as two isoforms of Tenascin C. Specificity of this MAb is validated by sequential immunoprecipitation with a PAb against Tenascin C. Tenascin C is a multifunctional, disulfide-linkedhexameric extracellular matrix glycoprotein expressed in association with mesenchymal epithelial interactions during development and in the neo-vasculature and stroma of undifferentiated tumors. In adults, it is restricted to certain epithelial-stromal interfaces and increases markedly in hyper-proliferative diseases and in stroma of many neoplasms, including gliomas, breast, squamous and lung carcinomas.
UOM:
1 * 50 µl
Fournisseur:
Sartorius
Description:
Cette pipette mécanique à grand écran a été conçue pour le confort. La Tacta rend le pipetage sûr et facile, et offre des résultats précis et fiables. Les matériaux utilisés pour la pipette ont été choisis avec soin, et chaque composant a été développé pour répondre aux normes les plus strictes.
Fournisseur:
Brady
Description:
L'imprimante industrielle à transfert thermique BradyPrinter i7100 est idéale pour les clients qui ont besoin d'imprimer de manière fiable de gros volumes sur de nombreux matériaux différents dans les secteurs de l'aérospatiale, de la défense et des transports en commun, de l'électronique, de l'automobile, de la logistique, de l'électricité, des télécommunications vocales et des marchés LAB.
Numéro de catalogue:
(BOSSBS-9982R-A680)
Fournisseur:
Bioss
Description:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9974R-A680)
Fournisseur:
Bioss
Description:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterisation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15130R-A680)
Fournisseur:
Bioss
Description:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15130R-A350)
Fournisseur:
Bioss
Description:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9979R-A680)
Fournisseur:
Bioss
Description:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterisation.
UOM:
1 * 100 µl
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est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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