4672 Results for: "Dodecyl+methacrylate&pageNo=54&view=list"

Supplier: KEYSTONE CLEANROOM PRODUCTS

Tyvek® 1422A autoclave bags with steam indicators can be used as either the inner, or outer bag for the steam sterilisation of pharmaceutical change parts.

Supplier: Bioss

Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Supplier: ROBU GLASFILTER

VitraPOR® glass filters are precision-engineered porous glass components for effective filtration in laboratory and industrial settings.

Supplier: Bioss

ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

Supplier: Bioss

ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

Supplier: OHAUS

Balances with multiple features, but uncomplicated weighing capabilities, provide the user with rapid, accurate results for routine weighing and measurement activities. Applications include weighing, formulation, check weighing and percentage weighing. Stabilisation times are typically less than three seconds.

Supplier: WTW

A wide choice of tests is available, for routine quantitative analysis in different applications, designed for use with WTW spectrophotometers and photometers. The test is automatically recognised by the laboratory instruments (via a barcoding system) and results are displayed in the appropriate units. Due to the different photometer optics, one test may yield different measuring ranges in different instruments; LED photometers may have smaller measuring ranges for the same test.

Supplier: Avantor

Avantor® ACE® AQ columns provide great reproducibility and column lifetime. These stainless steel columns are available in a wide range of particle sizes and dimensions from capillary to preparative.

Supplier: Bioss

Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Supplier: Bioss

ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

Supplier: Air Liquide

Possibility to upgrade an ARPEGE without electronic to a CRYOMEMO electronic. Please contact us for further information.

Supplier: Hettich

Powerful, compact bench top centrifuges with quiet and smooth running for processing microlitre tubes of 0,2 to 2,0 ml, used in clinical laboratories as well as in genetic research, virology and bacteriology.

Supplier: Hettich

Centrifuges with excellent performance and comprehensive range of accessories enabling them to carry out virtually any centrifuging task.

Supplier: OHAUS

Designed with energy efficiency in mind, the Compass CX series offers a battery life of up to 1000 continuous hours, allowing for uninterrupted operation. Compass™ CX scales have a stainless steel pan and are ideal for use in laboratory, industrial, education, and even household settings.

Supplier: Restek

Graphitised carbon black offers unique selectivity and very little adsorption for alcohol analyses. Two types of CarboBlack supports are available, CarboBlack B and CarboBlack C. CarboBlack B support, with its higher surface area, can hold up to a 10% loading of a non silicone liquid phase. CarboBlack C support can hold up to a 1% loading of a non silicone liquid phase.

Supplier: Greiner Bio-One

Flexibility is critical in terms of modern liquid handling solutions. This is why the Sapphire tips are manufactured in eight different sizes in a volume range from 10 to 1250 µl, including an extended length 10 µl tip for the recovery of small sample volumes. All our tips are made of medical grade polypropylene and are available as standard, low-retention, filter, or low-retention filter tips.

Supplier: MACHEREY-NAGEL

These ready-to-use Flash cartridges are designed for use in the Teledyne Isco® Companion® and other Teledyne Isco® CombiFlash® systems without additional connectors or capillaries or as stand-alone version for any pump/detector combinations.

Supplier: Avantor

These ultra-inert Avantor® ACE® C8 columns provide great reproducibility and column lifetime. These stainless steel columns are available in a wide range of particle sizes and dimensions from capillary to preparative.

Supplier: Bioss

Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Supplier: Cole Parmer

Advanced split beam optics ensure excellent accuracy and reproducibility.

Supplier: IKA

This overhead stirrer is ideal for special applications. Combining high performance with excellence, the units require minimum space.

Supplier: Bioss

Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Supplier: ROBU GLASFILTER

VitraPOR® glass filters are precision-engineered porous glass components for effective filtration in laboratory and industrial settings.

Supplier: SMEG

Glassware washing machines, LMP2010 jet rack with ¹/₄ position for test tube rack, 10 pipette wash positions and 20 assorted nozzle sizes, stainless steel, For: GW0160, GW0160S, GW1160, GW1160C, GW1160S, GW1160SC, GW3060BX, GW3060BXC, GW3060,P GW3060S

Supplier: Avantor

Avantor® ACE® C18-HL columns provide great reproducibility and column lifetime. These stainless steel columns are available in a wide range of particle sizes and dimensions from capillary to preparative.

Supplier: Rubbermaid Commercial Products

The Fast and Easy Solution for Washroom Hygiene.
Rubbermaid Toilet Seat Cleaner is a convenient and effective way to keep your washroom surfaces clean and germ-free. It is a simple and easy-to-use spray that removes dirt and bacteria from toilet seats, handles, or changing tables in seconds. Unlike messy and awkward seat covers, it dries quickly and leaves no residue. It also helps prevent the spread of diseases.

Supplier: Hettich

A rugged, versatile, indispensable centrifuge for routine laboratory tasks in doctors' practices and small hospital laboratories, especially for tasks in clinical chemistry and cytology as well as for the preparation of samples in industrial and research laboratories.

Supplier: Avantor

Avantor® ACE® AQ columns provide great reproducibility and column lifetime. These stainless steel columns are available in a wide range of particle sizes and dimensions from capillary to preparative.

Supplier: Bioss

Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf54 gene product has been provisionally designated C18orf54 pending further characterization.

Supplier: KEYSTONE CLEANROOM PRODUCTS

PureClean™ self-sealing autoclave bags are made from a transparent film and 1421B DuPont™ Tyvek®, which is a new grade of uncoated, untreated, flexible Tyvek® material specifically designed for pharmaceutical use in steam sterilisation applications. Uncoated Tyvek® eliminates the potential of residue deposits on equipment, post sterilisation.