sterile+vials
Numéro de catalogue:
(KIMB34155)
Fournisseur:
KIMBERLY CLARK
Description:
These single ply, light-duty wipes can handle a variety of delicate tasks and easily wipe up liquid and dust.
UOM:
1 * 17.160 ST
Fournisseur:
ANSELL HEALTH CARE
Description:
Glove liners made of high-elasticity polyamide for optimal fit.
Fournisseur:
Biowest
Description:
Donor horse serum is aseptically collected from herds of healthy animals inspected periodically by a licensed veterinarian. Applications for donor horse serum include mycoplasma contamination tests carried out on media, blocking agent and controls in immunoassays, culture of PC12 cells when combined with FBS.
Numéro de catalogue:
(331-0338)
Fournisseur:
BURKLE
Description:
La cuillère avec coque de cuillère coudée est appropriée pour des produits variés, par ex. la poudre, le granulé, les pâtes ou les liquides. La forme de cuillère coudée permet de bien atteindre aussi les coins d’un récipient. La cuillère en plastique à poignée longue permet une bonne vidange résiduelle d’un récipient de grande taille et accède également aux lieux difficilement accessibles, par ex. les bidon à goulot étroit.
UOM:
1 * 10 ST
Fournisseur:
Biowest
Description:
Feline serum is the liquid fraction of whole blood that is collected after the blood is allowed to clot; it is the blood plasma with the fibrinogens removed. Serum includes all proteins not used in blood clotting (coagulation) and all the electrolytes, antibodies, antigens, hormones, and any exogenous substances. Feline serum is used as a blocking agent in immunoassays and controls.
Fournisseur:
ANSELL HEALTH CARE
Description:
Ansell's lightest ANSI A5/ISO Level E cut resistant touchscreen glove.
Numéro de catalogue:
(BOSSBS-9098R-HRP)
Fournisseur:
Bioss
Description:
ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9098R-A647)
Fournisseur:
Bioss
Description:
ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1021R-A350)
Fournisseur:
Bioss
Description:
Cooperates with LY96 and CD14 to mediate the innate immune response to bacterial lipopolysaccharide (LPS). Acts via MYD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also involved in LPS-independent inflammatory responses triggered by free fatty acids, such as palmitate. In complex with TLR6, promotes sterile inflammation in monocytes/macrophages in response to oxidized low-density lipoprotein (oxLDL) or amyloid-beta 42. In this context, the initial signal is provided by oxLDL- or amyloid-beta 42-binding to CD36. This event induces the formation of a heterodimer of TLR4 and TLR6, which is rapidly internalized and triggers inflammatory response, leading to the NF-kappa-B-dependent production of CXCL1, CXCL2 and CCL9 cytokines, via MYD88 signaling pathway, and CCL5 cytokine, via TICAM1 signaling pathway, as well as IL1B secretion.
UOM:
1 * 100 µl
Numéro de catalogue:
(218-1290)
Fournisseur:
Bel-Art Products, a Part of SP
Description:
En PP, autoclavable.
UOM:
1 * 1 ST
Fournisseur:
BURKLE
Description:
PS. Double pelle-spatule à extrémités arrondies, contenu 1,0 et 0,25 ml. La micro-spatule à usage unique permet d'échantillonner, de transvaser ou de transformer de petites quantités de produits chimiques, poudres, granulés, pâtes, crèmes ou liquides.
Fournisseur:
Thermo Fisher Scientific
Description:
Use SureSTART™ level 3 manual vial crimpers for 20 mm Crimp vials to ensure that your crimp caps are sealed reliably every time.
Fournisseur:
PerkinElmer
Description:
Bouchon pour flacon de chromatographie, Phénolique, Ø: 13 mm, Screw cap, without septa, Septum: –
Numéro de catalogue:
(BOSSBS-9617R-CY3)
Fournisseur:
Bioss
Description:
C14orf174, is a 674 amino acid protein that contains one SAM (sterile alpha motif) domain. Existing as two alternatively spliced isoforms,C14orf174 is encoded by a gene that maps to human chromosome 14q24.3. Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein Bcl-3 in the (14;19) translocations found in a variety of B cell malignancies.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9617R)
Fournisseur:
Bioss
Description:
C14orf174, is a 674 amino acid protein that contains one SAM (sterile alpha motif) domain. Existing as two alternatively spliced isoforms,C14orf174 is encoded by a gene that maps to human chromosome 14q24.3. Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein Bcl-3 in the (14;19) translocations found in a variety of B cell malignancies.
UOM:
1 * 100 µl
Numéro de catalogue:
(PERCN6101182)
Fournisseur:
PerkinElmer
Description:
This is a replacement vial locator for PerkinElmer AutoSystem GC autosamplers.
UOM:
1 * 1 ST
Appel de prix
Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l' est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l' est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
Ces articles ne peuvent être ajoutés au Panier. Veuillez contacter votre service client ou envoyer un e-mail à vwr.be@vwr.com
Une documentation supplémentaire peut être nécessaire pour l'achat de cet article. Un représentant de VWR vous contactera si nécessaire.
Ce produit a été bloqué par votre organisation. Contacter votre service d'achat pour plus d'informations.
Le produit original n'est plus disponible. Le remplacement représenté est disponible
Les produits marqués de ce symbole ne seront bientôt plus disponibles - vente jusqu'à épuisement de stock. Des alternatives peuvent être disponibles en recherchant le code article VWR indiqué ci-dessus. Si vous avez besoin d'une assistance supplémentaire, veuillez contacter notre Service Clientèle au 016 385 011.
|
|||||||||