10985 Results for: "Obaly+steriliza\\\\\\\\\\\\\\\\u010Dn\u00ED&pageNo=21"

Supplier: DWK Life Sciences

CryoELITE® cryogenic vials are made from low binding, cryogenic grade virgin PP. They offer an unrivaled cap seal for the shipping and storage of precious biosamples. The patented cap seal exceeds DOT and IATA regulations ensuring ultimate protection of samples during transportation and demanding freeze-thaw handling.

Supplier: VWR Collection

ESD kalhoty jsou vyrobeny z 63% polyesteru, 35% bavlny a 2% rezistentního vlákna (uhlíku). Tato speciální směs zajišťuje stálou antistatickou ochranu. Díky tomu jsou tyto kalhoty vhodné pro použití v prostředí výroby elektroniky.

Supplier: Avantor Fluid Handling

Protect your light-sensitive samples.

Supplier: Avantor Fluid Handling

Provides longer life than other platinum and peroxide silicone tubing formulations.

Supplier: Avantor Fluid Handling

Ensure optimum performance from your Masterflex® pump.

Supplier: VWR Collection

Ekonomická řada spolehlivých, vysoce výkonných analytických vah. Všechny modely mají nerezovou vážní desku.

Supplier: Avantor Fluid Handling

Ultra low spallation protects fluid purity – ideal for sensitive and costly fluids and for filtration applications.

Supplier: Halyard

PUREZERO* HG5 gloves feature an accelerator-free formulation that reduces the risk of allergies and skin irritation associated with accelerator chemicals in other nitrile gloves. Comfortable to wear, the HG5 gloves also protect workers with effective barrier protection against chemical splash, micro-organisms, and viruses.

Supplier: LABCONCO

Fast-Freeze® flasks for FreeZone® freeze dry systems are designed to be easier to handle, faster to load, and more convenient to use in the laboratory for freeze drying.

Supplier: GA

Cryogenic direct thermal labels intended for labeling already frozen surfaces and containers under deep-freeze conditions, as low as (–80 °C).

Supplier: ECOLAB CONTAMINATION CONTROL

Contains 70% IPA or denatured ethanol (IMS) blended with highest specification (EP) water for injection. It is filtered to 0,2 µm, filled and triple bagged under ISO Class 5; Grade B (microbial count) laminar flow in an ISO Class 7; Grade C (microbial count) cleanroom before irradiation using a validated process at no less than 25 kGy to ensure spore free alcohol.

Supplier: GA

Writable cryogenic colour dots and rectangles provided in dispenser box rolls for identifying the sides and tops of cryo vials and microtubes stored in lab freezers and liquid nitrogen dewars. Easy to write on with permanent cryo markers, JTRA-class labels are available in a variety of colours.

Supplier: FRISTADS KANSAS

Basic T-shirts made of 100% pre-shrunk, ring spun cotton (single jersey). The models in mottled grey are made of 85% cotton and 15% viscose.

Supplier: Antibodies.com

Human MYH7B ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MYH7B in serum, plasma, tissue homogenates or other biological fluids.

Supplier: FRISTADS KANSAS

Jacket made of 65% polyester and 35% cotton, ideal for light-duty industrial applications. Made for the industrial worker with emphasis on comfort, durability and functionality.

Supplier: ProSci Inc.

Calcitonin is a secreted protein which belongs to the calcitonin family. Calcitonin is cleaved into the following two chains: Calcitonin and Katacalcin. Katacalcin is a potent plasma calcium-lowering peptide. Calcitonin is a 32-amino acid linear polypeptide hormone. Calcitonin acts to reduce blood calcium (Ca2+), opposing the effects of parathyroid hormone (PTH). Its importance in humans has not been as well established as its importance in other animals, as its function is usually not significant in the regulation of normal calcium homeostasis. Calcitonin causes a rapid but short-lived drop in the level of calcium and phosphate in blood by promoting the incorporation of those ions in the bones.

Supplier: PEAK SCIENTIFIC

Precision Nitrogen 250 generator provides a constant and consistent source of nitrogen for detector make-up gas at standard/typical detection levels for GC applications, as well as headspace vial pressurization, purge and trap, tube conditioning for thermal desorption and sample preparation.

Supplier: GA

These freezer grade blackout labels are designed to conceal any already existing information or labels. Can be used to re-label cryo vials, microtubes, and freezer boxes stored in ultra-low temperature freezers (−80 °C) or transported in dry ice.

Supplier: FRISTADS KANSAS

Gilets made from 65% polyester and 35% cotton; napped inner.

Supplier: Antibodies.com

Mouse CCL21 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse CCL21 in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.

Supplier: Cytiva (Formerly Pall Lab)

A filter for every step in your process. From drug discovery and basic research to process development, Pall Laboratory's AcroPak capsules come in a variety of membrane types and volume sizes.

Supplier: Bioss

The downstream of kinase family (Dok1-7) are members of a class of docking? proteins that include the tyrosine kinase substrates IRS-1 and Cas, which contain multiple tyrosine residues and putative SH2 binding sites. Based on their similarities, the Dok family of proteins can be divided into three subgroups: Dok-1/2/3, Dok-4/5/6 and Dok-7. Through its interaction with muscle-specific receptor kinase (MuSK), Dok-7 is crucial for neuromuscular synaptogenesis and for MuSK activation. Mice lacking Dok-7 do not form neuromuscular synapses nor acetylcholine receptor clusters. Mutations in the Dok-7 gene can cause congenital myasthenic syndromes (CMA) recessively inherited disorders characterized by muscle weakness.

Supplier: Bioss

Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf117 gene product has been provisionally designated C20orf117 pending further characterization.

Supplier: Bioss

Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

Supplier: JULABO GmbH

VALEGRO recirculating coolers are environmentally-friendly all-rounders for a wide range of temperature control tasks. They are characterised by a good ratio between cooling capacity and unit size as well as optimal usability. They work with natural refrigerant and can be adapted to application requirements thanks to their adjustable pump.

Supplier: Bioss

Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf38 gene product has been provisionally designated C3orf38 pending further characterization.

Supplier: Bioss

Hephaestin is a single-pass type I membrane protein that belongs to the multicopper oxidase family of proteins. Hephaestin, a copper-dependant ferroxidase protein, is crucial for iron exiting intestinal enterocytes into the circulation. It mediates the movement of iron across the basolateral membrane in conjunction with ferroportin 1. This is an important link between iron and copper metabolism in mammalian systems, as copper deficiency leads to reduced hephaestin and reduced iron absorption resulting in anemia. Hephaestin can bind six copper ions per monomer and is regulated by the homeobox transcription factor CDX2. Increased levels of iron leads to an increase in CDX2 expression and thus Hephaestin. Hephaestin is primarily detected in the intestine, but is also expressed in colon, breast, bone trabecural cells and fibroblasts.

Supplier: Bioss

Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf40 gene product has been provisionally designated C4orf40 pending further characterization.

Supplier: Bioss

Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf151 gene product has been provisionally designated C20orf151 pending further characterization.

Supplier: Bioss

Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf117 gene product has been provisionally designated C20orf117 pending further characterization.