6624 Results for: "Plant+Learning+Activities&pageNo=41&view=list"

Supplier: OHAUS

This incubating/cooling orbital shaker is microplate ready without the need for any additional accessories. Optional modular blocks can accommodate micro-tubes, centrifuge tubes, vials, or culture tubes. Unit holds microplates or modular blocks with a 127 mm tall interior capacity. Ideal for analyses that require a stable, controlled temperature.

Supplier: CHIRAL TECHNOLOGIES

These columns allow chromatographers to employ essentially any organic solvent as mobile phase to develop methods for the most challenging separations. These columns are available in a variety of particle sizes and offer great speed and column resolving power. Columns packed with 3 µm CSPs offer high speed separations and a reduction in analysis time and cost per sample. Columns, packed with 3 µm particles, may be used in conventional HPLC units without significant loss in performance, even with the smaller column dimensions.

Supplier: FRISTADS KANSAS

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

Supplier: FRISTADS KANSAS

Two-colour working trousers with contrast stitching, made of 65% polyester and 35% cotton.

Supplier: FRISTADS KANSAS

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

Supplier: PEAK SCIENTIFIC

The Precision Zero Air generators are designed specifically to supply clean, dry, hydrocarbon-free air to be used as flame support gas for GC at both standard and trace detection limits.

Supplier: MICROSOLV

RSA™ (Reduced Surface Activity) high quality and extremely consistent autosampler vials and caps due to reduced surface activity glass manufacturing and control processes. Excellent for low abundance or low dosage form analytes or samples that are pH sensitive, or basic in nature.

Supplier: FRISTADS KANSAS

Functional vests made from 65% polyester and 35% cotton; with napped inner.

Supplier: MACHEREY-NAGEL

NUCLEODUR® C8 ec is a medium density monomeric octyl modified silica phase for HPLC.

Supplier: VWR Collection

Rugged and economical balances, that are ideal for educational establishments and laboratory use. A series that ranges from simple weighing to operation with automated internal calibration. All Classic models have a simple backlit LCD with adjustable contrast and ergonomic keypad and a stainless steel top pan.

Supplier: MOLECULAR DEVICES

The SpectraMax® iD5 multi-mode microplate reader is a complete laboratory solution to increase your research capabilities and comes with built-in absorbance, fluorescence, luminescence, time-resolved fluorescence (TRF) and tuneable fluorescence polarisation (FP) read modes. In addition, the SpectraMax® iD5 can be expanded to include bottom-read luminescence, TR-FRET, HTRF®, BRET, dual luciferase reporter assays with injectors and Western blot detection.

Supplier: Avantor Fluid Handling

Versatile pumps for process applications - with an intuitive touch-screen interface and advanced connectivity. This drive offers a broad flow range, from 0,0006 to 19 LPM, adaptable to a variety of applications and workflows. The drive housing is constructed of 316 stainless steel - IP 66 and NEMA 4X rated for washdown.

Supplier: OHAUS

Large platform bench scales that incorporate touch screen, advanced weighing and proximity sensor technologies. The easy to use control unit can be mounted on the base, above the base on an optional column, on a wall, or remotely (up to 3 metres distance with an optional cable). The touch screen display, with universal icons and informative prompts, simplifies set-up functions and basic operation. The operator has the added choice to use proximity sensors for hands-free operation for handling sensitive samples. The balances have multiple application modes for basic weighing to SQC applications together with short stabilisation times and optimised performance specifications.

Supplier: bimos

Neon supports the forward-leaning sitting position that is often necessary in lab work. Its modern design matches the high-tech laboratory environment perfectly and of course it has all the characteristics you would expect of a good laboratory chair. It is seamless, easy to clean, washable, and resistant to disinfectants. So, Neon is the ideal solution for the laboratory, when a really comfortable ergonomic chair is needed.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: FRISTADS KANSAS

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

Supplier: Kango

Ergonomic and auto-adaptive chairs or stools made from soft PU or wood.
Nobody has perfect symmetrical morphology. This is why people have back problems, sometimes with a feeling of heavy legs. The answer to this problem can be found in the main features of the Koncept chairs and stools.

Supplier: Merck

Syringe filters are single-use, membrane-based devices used for the removal of particulate impurities from liquid and gas samples prior to analysis by methods such as HPLC, ion chromatography, gas chromatography, ICP, and dissolution testing. Proper filtration of samples improves the quality and consistency of analytical results and decreases instrument downtime.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: Bioss

Myotrophin (V-1 protein) is a ubiquitously expressed cytoplasmic protein that can translocate to the nucleus during sustained NFkB activation. The gene encoding for this protein localizes to chromosome 7q33. Myotrophin may be involved in cerebellar morphogenesis and contains an acetylated N-terminus and 2.5 internal 33 amino acid ankyrin repeats. It is important in the differentiation of cerebellar neurons, particularly of granule cells. The 117 amino acid protein has been associated with, and able to induce, cardiac hypertrophy. Myotrophin increases protooncogene, ANF and Beta-Myosin heavy chain transcript levels. Myotrophin is upregulated when myocytes undergo cyclic stretch or are treated with tumour necrosis factor Alpha (TNF Alpha) or interleukin-1Beta. Highest levels of Myotrophin are detected in brain and lowest levels in skeletal muscle.

Supplier: asecos

Fireproof safety cabinets, classified type 30 (fire resistant up to 30 minutes), safe, durable, robust and convenient with transport base and bicoloured cabinet design.

Supplier: Avantor

Avantor® ACE® Method Development Kits (MDK) are designed to maximise selectivity, offering a powerful and reliable approach to UHPLC/HPLC method development. Based upon an ultra-inert, high efficiency silica, Avantor® ACE® phases incorporate the latest developments in LC stationary phase design, providing chromatographers with more choices for alternative selectivity, without compromising stability or robustness.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: Bioss

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterisation.

Supplier: Bioss

Myotrophin (V-1 protein) is a ubiquitously expressed cytoplasmic protein that can translocate to the nucleus during sustained NFkB activation. The gene encoding for this protein localizes to chromosome 7q33. Myotrophin may be involved in cerebellar morphogenesis and contains an acetylated N-terminus and 2.5 internal 33 amino acid ankyrin repeats. It is important in the differentiation of cerebellar neurons, particularly of granule cells. The 117 amino acid protein has been associated with, and able to induce, cardiac hypertrophy. Myotrophin increases protooncogene, ANF and Beta-Myosin heavy chain transcript levels. Myotrophin is upregulated when myocytes undergo cyclic stretch or are treated with tumour necrosis factor Alpha (TNF Alpha) or interleukin-1Beta. Highest levels of Myotrophin are detected in brain and lowest levels in skeletal muscle.

Supplier: ANTIBODIES.COM

Human SPTBN2 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SPTBN2 in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: MACHEREY-NAGEL

NUCLEODUR® C18 Gravity is an octadecyl modified silica phase with a high density coverage, using for HPLC.

Supplier: FRISTADS KANSAS

Industrial jacket made of 65% polyester and 35% cotton, with soft nap on reverse side. The royal blue jacket is available with different accent and piping colours.