6223 Results for: "4-Methylbenzyl+isothiocyanate&pageNo=31&view=easy"

Supplier: FRISTADS KANSAS

Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.

Supplier: LAUDA

Baths/circulation thermostats with plain text menu navigation which are ideal for user friendly operation.

Supplier: FRISTADS KANSAS

Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.

Supplier: Antibodies.com

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

Supplier: Antibodies.com

Bovine BNP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of bovine BNP in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Antibodies.com

Porcine BNP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of porcine BNP in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Antibodies.com

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

Supplier: Antibodies.com

Rat BNP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat BNP in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Antibodies.com

Human TPSG1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human TPSG1 in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Bioss

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf111 gene product has been provisionally designated C1orf111 pending further characterization.

Supplier: Bioss

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf111 gene product has been provisionally designated C1orf111 pending further characterization.

Supplier: Bioss

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf54 gene product has been provisionally designated C1orf54 pending further characterization.

Supplier: Bioss

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf54 gene product has been provisionally designated C1orf54 pending further characterization.

Supplier: Bioss

Comparative evaluation of the expression patterns of the human and mouse genes, combined with previous biochemical and yeast genetic studies, indicate that the Exo1 (Exonuclease I) proteins are important contributors to chromosome processing during mammalian DNA repair and recombination. In mice, the Exo1 gene maps to distal chromosome 1, consistent with the recent mapping of the orthologous human HEX1/EXO1 gene to chromosome 1q43. Exo1 is expressed prominently in testis, an area of active homologous recombination, and spleen, a prominent lymphoid tissue. In both mammalian and yeast systems, Exo1 is a 5'-3' double stranded DNA exonuclease that has previously been implicated in DNA mismatch repair (MMR). The MMR system ensures genome integrity by removing mispaired and unpaired bases that originate during replication. In humans, Exo1 interacts with MSH2 and MLH1 and has been proposed to be a redundant exonuclease in MMR. In both mammalian and yeast systems, Exo1 plays a structural role in MMR and stabilises multiprotein complexes containing a number of MMR proteins.

Supplier: Bioss

TANC (tetratricopeptide repeat, ankyrin repeat and coiled-coil domain-containing protein), also known as TANC1, is a 1861 amino acid postsynaptic cell membrane protein that contains eleven ANK repeats, three TPR repeats and belongs to the TANC family. Considered a scaffolding component in the postsynaptic density, TANC interacts with TNIK, SAPAP1, Alpha-internexin, CaMKII, NMDA 2 and GluR-1. It is also thought that TANC interacts directly with SAP 97, PSD-95 and Homer. Upon stimulation by Rap 2, MINK1 and TNIK may phosphorylate TANC. The TANC gene encodes two alternatively spliced isoforms, contains approximately 264025 bases and maps to human chromosome 2q24.2. Making up approximately 8% of the human genome, chromosome 2 consists of 237 million bases and encodes over 1400 genes. A number of genetic diseases are linked to genes on chromosome 2 including Harlequin icthyosis, sitosterolemia and Alstr syndrome.

Supplier: Bioss

The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins. The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes. Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity. Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health. Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13. Tim8A is highly expressed in fetal and adult brain. Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system.

Supplier: Avantor Fluid Handling

High-flow pump for process applications – with an intuitive touch-screen interface and advanced connectivity.

Supplier: Binder

Avantgarde. Line incubators ensure stable and reliable incubation of microbiological cultures and guarantee reproducible results for routine tests in the laboratory – even high batch throughputs and with long-term operation. Avantgarde. Line BD models have natural convection ensuring rapid temperature equalisation after the door is opened. The BF models have forced convection via a fan. The APT.line™ pre-heating chamber technology gives homogeneous temperature distribution, excellent temperature uniformity and low fluctuation. Units up to 115 litres can be stacked on top of each other to save space. The units have 60 mm insulation which lowers energy consumption and increases performance. All models have a stainless steel chamber with an ergonomic door opening system.

Supplier: Binder

These energy efficient cooled incubators have been designed for use in the temperature range from 4 to 100 °C. They feature a Peltier cooling system for finely controlled cooling down to 4 °C together with powerful conventional heating. The unit has easy to clean stainless steel interior and inner safety glass door. The incubators are ideal for use in microbiology, genetics, zoology, food and beverage industries, medicine, forensics, pharmaceutical and cosmetic industries. USB port for reading data and ethernet interface for communication software APT-COM™ DataControlSystem.

Supplier: Bioss

Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin-1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterised by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt's lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.

Supplier: JULABO GmbH

High temperature circulators can be used for temperature applications up to 400 °C; units provide powerful heating capacities for shortest heat-up times and rapid compensation of endothermic reactions. Applications include use with reactors, autoclaves, distillation columns, mini plant installations, pilot plants and production facilities. Because of the closed circuit system oxidation is reduced and unpleasant odours and vapours do not escape, even at high temperatures.

Supplier: Thermo Fisher Scientific

This RO system with controller provides easy-to-read system parameters. Completely drainable, integrated 100 L high-purity water reservoir has a low-noise pressure booster as a standard component. The compact LabTower RO system is ideally suited as a feed water source for dishwashers, autoclaves and general laboratory use. It serves as a built-in pretreatment unit, consisting of a hardness stabilizer for protection of reverse osmosis module from hardness formers. An activated carbon/5 μm combi-cartridge protects the system against free chlorine and particles which ensures the long service life of downstream purification stages.

Supplier: Merck

The Aquastar® range is designed to provide reagents for the determination of water by Karl Fischer titration of a wide range of substrates and by a variety of methodologies. These include reagents for one- or two-component systems; combined coulometric reagents; solvents for oils and fats; reagents and solvents for determination of water in ketones and aldehydes. Calibration standards are also available.

Supplier: Bioss

Comparative evaluation of the expression patterns of the human and mouse genes, combined with previous biochemical and yeast genetic studies, indicate that the Exo1 (Exonuclease I) proteins are important contributors to chromosome processing during mammalian DNA repair and recombination. In mice, the Exo1 gene maps to distal chromosome 1, consistent with the recent mapping of the orthologous human HEX1/EXO1 gene to chromosome 1q43. Exo1 is expressed prominently in testis, an area of active homologous recombination, and spleen, a prominent lymphoid tissue. In both mammalian and yeast systems, Exo1 is a 5'-3' double stranded DNA exonuclease that has previously been implicated in DNA mismatch repair (MMR). The MMR system ensures genome integrity by removing mispaired and unpaired bases that originate during replication. In humans, Exo1 interacts with MSH2 and MLH1 and has been proposed to be a redundant exonuclease in MMR. In both mammalian and yeast systems, Exo1 plays a structural role in MMR and stabilizes multiprotein complexes containing a number of MMR proteins.

Supplier: S.C.A.T.

The SCAT SafetyWasteCaps provide maximum safety for your HPLC liquid disposal. Safely dispose of your liquid laboratory waste without contaminating the ambient air by using SafetyWasteCaps with integrated exhaust air filters. These high-performance filters regulate the air pressure balance and prevent the escape of vapors due to the resulting overpressure in the disposal container. The variety of closures, connections and thread sizes allows optimal adaptation to your HPLC situation. Additional versions with grounding connections, level controls or safety funnels or offer every convenience for safe disposal.

Supplier: MEMMERT

Sets eco standards for cultivation below room temperature: Unmatched energy efficiency, excellent heat-up, cool-down and recovery times.

Supplier: Cole-Parmer

Patented block and optical technologies deliver extreme speed, sensitivity, and data quality.

Supplier: FRISTADS KANSAS

Thanks to its durability and high degree of comfort, the PR54 jacket is perfectly suited to workshops and industrial and service enterprises. The material is made from 65% polyester and 35% cotton. The inside is brushed and as a result conveys a pleasantly comfortably cotton feeling. The outside is also resistant to the roughest demands and will not fade even after countless washes.

Supplier: IKA

Regardless of whether samples are hard, soft or fibrous this MultiDrive crusher can perform a wide range of crushing tasks involving coarse and fine crushing. MultiDrive control mixes, grinds and is also fitted with a dispersion vessel and a disposable tube.

Supplier: UVP ULTRA VIOLET PRODUCTS

Cabinet c-10e cabinet only - add 4w el lamp 1 * 1 items