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Masterflex+Single-use+Flow+Sensor
Numéro de catalogue:
(BOSSBS-5405R-A680)
Fournisseur:
Bioss
Description:
KRT18 encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. Mutations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for this gene.
UOM:
1 * 100 µl
Fournisseur:
Biotium
Description:
This MAb is specific to c-erbB-2/HER-2 and shows minimal cross-reaction with other members of the family. C-erbB-2/HER-2 is a member of the EGFR family. Receptors of this family are located on the plasma membrane and consist of an extracellular ligand-binding domain that is connected to a large intracellular domain by a single transmembrane sequence. c-erbB-2/HER-2 protein is over-expressed in a variety of carcinomas especially those of breast and ovary.
Numéro de catalogue:
(BOSSBS-5405R-A647)
Fournisseur:
Bioss
Description:
KRT18 encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. Mutations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
UOM:
1 * 100 µl
Fournisseur:
Molecular Devices
Description:
Le lecteur de microplaques SpectraMax® L mesure les tests de luminescence flash et glow dans des plaques à 96 et 384 puits.
Fournisseur:
BD Medical
Description:
The BD CPT™ glass tube provides a single-step, standardised method for the isolation of Peripheral Blood Mononuclear Cells (PBMCs) - lymphocytes and monocytes from whole blood. In a single process step, up to 15 million PBMCs can be isolated within 20 minutes.
Fournisseur:
Simport Scientific
Description:
Ces chambres se mettent facilement en place, permettant au filtre de s'aligner correctement avec le tunnel à échantillons. Elles sont équipées d'un anneau de compression, situé autour de l'orifice pour échantillons, afin de mieux contrôler le taux d'absorption et de garantir des résultats cohérents. Deux ports, l'un dans le puits à échantillons et l'autre dans le tunnel permettent une grande flexibilité. Les échantillons sont chargés par les bouchons du godet afin d'éviter les éclaboussures d'échantillons dangereux. Les bouchons procurent une sécurité supplémentaire à l'utilisateur. Une grande zone de dépôt de cellules, centrée, facilite le criblage et le rend plus sensible. Dans les chambres doubles, les zones de dépôt de cellules sont plus proches et faciles à trouver, ce qui permet d'accélérer l'analyse des échantillons. Deux zones de dépôt sur une lame améliorent tous les avantages des chambres simples classiques. Gain de temps pour le chargement et le déchargement des lames.
Fournisseur:
SGE a Trajan company
Description:
A connecting unit with inlet and outlet connectors for the gas lines.
Numéro de catalogue:
(BOSSBS-4757R-A647)
Fournisseur:
Bioss
Description:
Involved in diverse cellular processes such as ribosome biogenesis, centrosome duplication, protein chaperoning, histone assembly, cell proliferation, and regulation of tumor suppressors p53/TP53 and ARF. Binds ribosome presumably to drive ribosome nuclear export. Associated with nucleolar ribonucleoprotein structures and bind single-stranded nucleic acids. Acts as a chaperonin for the core histones H3, H2B and H4. Stimulates APEX1 endonuclease activity on apurinic/apyrimidinic (AP) double-stranded DNA but inhibits APEX1 endonuclease activity on AP single-stranded RNA. May exert a control of APEX1 endonuclease activity within nucleoli devoted to repair AP on rDNA and the removal of oxidized rRNA molecules. In concert with BRCA2, regulates centrosome duplication. Regulates centriole duplication: phosphorylation by PLK2 is able to trigger centriole replication. Negatively regulates the activation of EIF2AK2/PKR and suppresses apoptosis through inhibition of EIF2AK2/PKR autophosphorylation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-4757R-A555)
Fournisseur:
Bioss
Description:
Involved in diverse cellular processes such as ribosome biogenesis, centrosome duplication, protein chaperoning, histone assembly, cell proliferation, and regulation of tumor suppressors p53/TP53 and ARF. Binds ribosome presumably to drive ribosome nuclear export. Associated with nucleolar ribonucleoprotein structures and bind single-stranded nucleic acids. Acts as a chaperonin for the core histones H3, H2B and H4. Stimulates APEX1 endonuclease activity on apurinic/apyrimidinic (AP) double-stranded DNA but inhibits APEX1 endonuclease activity on AP single-stranded RNA. May exert a control of APEX1 endonuclease activity within nucleoli devoted to repair AP on rDNA and the removal of oxidized rRNA molecules. In concert with BRCA2, regulates centrosome duplication. Regulates centriole duplication: phosphorylation by PLK2 is able to trigger centriole replication. Negatively regulates the activation of EIF2AK2/PKR and suppresses apoptosis through inhibition of EIF2AK2/PKR autophosphorylation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-5009R-HRP)
Fournisseur:
Bioss
Description:
Phosphorylase b kinase catalyzes the phosphorylation of serine in certain substrates, including troponin I. Polymer of 16 chains, four each of alpha, beta, gamma, and delta. Alpha and beta are regulatory chains, gamma is the catalytic chain, and delta is calmodulin. The two calmodulin-binding domains appear to act in concert to bind a single molecule of calmodulin and are pseudosubstrate/autoinhibitory domains.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13352R-A750)
Fournisseur:
Bioss
Description:
This gene encodes a member of the gamma-glutamyl transpeptidase (GGT) family, which are important in the metabolism of glutathione. The most ubiquitously expressed human GGT gene, GGT1, encodes a single transmembrane polypeptide that is post-translationally processed to form a heavy and a light chain. In contrast, the product of this gene only contains homology to the light chain region, and lacks a transmembrane domain. Multiple alternatively spliced variants, encoding the same protein, have been identified.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1677R-CY3)
Fournisseur:
Bioss
Description:
Efficiently joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. Involved in DNA non-homologous end joining (NHEJ) required for double-strand break repair and V(D)J recombination. The LIG4-XRCC4 complex is responsible for the NHEJ ligation step, and XRCC4 enhances the joining activity of LIG4. Binding of the LIG4-XRCC4 complex to DNA ends is dependent on the assembly of the DNA-dependent protein kinase complex DNA-PK to these DNA ends.
UOM:
1 * 100 µl
Fournisseur:
CPC COLDER
Description:
Connectors provide quick and easy sterile connections for small-flow applications, even in non-sterile environments.
Numéro de catalogue:
(BOSSBS-2526R-A555)
Fournisseur:
Bioss
Description:
CD160, a 27 kDa glycoprotein, was initially identified with the monoclonal antibody BY55. Its expression is tightly associated with peripheral blood NK cells and CD8 T lymphocytes with cytolytic effector activity. The cDNA sequence of CD160 predicts a cysteine rich, glycosylphosphatidylinositol anchored protein of 181 amino acids with a single Ig-like domain weakly homologous to KIR2DL4 molecule.
UOM:
1 * 100 µl
Fournisseur:
VWR Collection
Description:
ChromasterUltra Rs, ChromasterUltra Rs, unité à cuve de circulation pour détecteur à réseau de diodes 6430 (chemin 10 mm, volume 2,2 µl)
Numéro de catalogue:
(BOSSBS-8480R)
Fournisseur:
Bioss
Description:
RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions that affect males more frequently as males carry a single X chromosome.
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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