6217 Results for: "Comparator+Kits&pageNo=31&view=list"

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: Avantor Fluid Handling

Designed with maintenance-free high-accuracy motor and a graphical interface—makes setup and operation easier than ever!

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: SCHOTT AG Lighting and imaging

The SCHOTT EasyLED portfolio for stereo microscopy delivers precise LED light for a wide variety of applications, such as laboratory and diagnostics, industrial applications, education, or forensic science. The series offers robust design and easy handling in a compact device, with a range of accessories for specific requirements.

Supplier: Avantor Fluid Handling

Maintenance-free drives built for precision dispensing.

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: VWR Collection

VENTI-Line® drying ovens are designed for all standard drying and tempering tasks as well as sterilising glassware. They have a temperature range between 50 to 300 °C and are intended for use in biological, chemical, medical, pharmaceutical and physical laboratories.

Supplier: VWR Collection

PE bags, transparent. These sterile sampling bags provide a secure, contaminant-free pliant container that ensures dependable analysis results. Economical and efficient way to collect, contain and carry samples. With these bags, the user can bring sterile sampling bags into a cleanroom without any worries about contamination. The bags are double-pouched so the user can remove the outer bag before entering the cleanroom, which minimises the number of bags exposed.

Supplier: Merck

All Spectroquant® test kits can be used with the Prove range of spectrophotometers and Nova 60/60A instruments. Tests can be used not only on photometers and spectrophotometer from Merck, but also on photometers and spectrophotometers from other suppliers (programming details available on request). Spectroquant® cell test kits.

Supplier: FRISTADS KANSAS

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

Supplier: FRISTADS KANSAS

This outdoor jacket is made of anti-pilling polyester, jersey bonded fabric, with micro fleece inside. The jacket is windproof, water repellent, breathable and quick drying.

Supplier: FRISTADS KANSAS

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

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: MACHEREY-NAGEL

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

Supplier: Thermo Fisher Scientific

Contains a C4 linker which allows for superior alignment of the phenyl ring with aromatic molecules. Get excellent retention and unique selectivity for aromatic and moderately polar analytes with Thermo Scientific™ Hypersil GOLD™ Phenyl reversed phase HPLC columns.

Supplier: Thermo Fisher Scientific

Ambient measurements or monitoring of laboratory equipment.

Supplier: Thermo Fisher Scientific

Natural tubes are made from 100% virgin PP to help ensure maximum clarity for biological-based work.

Supplier: Avantor Fluid Handling

Versatile pumps for accurate fluid delivery – with an intuitive touch-screen interface.

Supplier: VWR Collection

The W10 heating plate, with its sleek compact design, accommodates two rows of up to 40 slides in total. The heating plate is very useful as a stretch bench for mounting, stretching and drying paraffin sections on slides, fixing bacterial smears, and heating fluid samples in Petri dishes. The black anodised surface provides an excellent visual contrast. The working plate is made of solid 8 mm aluminium with black anodised surface and ensures a constant, homogenous temperature over the entire heating surface. The touch display and switch are protected from water and paraffin. The unit has over-temperature protection for extra safety. Temperature adjustment and power On/Off switch, with control light for 'On' mode, are conveniently located at the front of the unit.

Supplier: VWR Collection

DRY-Line® drying ovens are designed for all standard drying and tempering tasks as well as sterilising glassware. They have a temperature range between 50 to 300 °C and are intended for use in biological, chemical, medical, pharmaceutical and physical laboratories.

Supplier: TEKNOMEK

Our range of sensor operated wash troughs are manufactured from 304 grade stainless steel with a fully welded design for maximum hygiene. Choose from knee, battery or mains operation to suit your needs.

Supplier: MACHEREY-NAGEL

NUCLEODUR® C18 PolarTec is an octadecyl modified silica phase with embedded polar group for HPLC.

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 C9orf71 gene product has been provisionally designated C9orf71 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 C9orf71 gene product has been provisionally designated C9orf71 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 C9orf50 gene product has been provisionally designated C9orf50 pending further characterisation.

Supplier: Bioss

The charged multivesicular body proteins, commonly designated CHMPs, belong to the vacuolar sorting protein family and function as chromatin-modifying proteins. CHMP1-6 are all components of ESCRT (endosomal sorting complex required for transport) I, II or III complexes. These complexes are crucial for sorting endosomal articles into multivesicular bodies (MVBs), and are also required for the formation of these bodies. CHMP2B, also known as CHMP2.5 or vacuolar protein-sorting-associated protein 2-2, is a 213 amino acid cytosolic protein. Widely expressed in brain, heart, skeletal muscle, small intestine, pancreas, lung, placenta and leukocytes, CHMP2B associates directly with CHMP2A and vps4 for the disassembly of the ESCRT-III complex. Defects in the gene encoding CHMP2B have been shown to cause chromosome 3-linked frontotemporal dementia (FTD3).

Supplier: Bioss

The CART gene encodes for a protein which has an important role in the regulation of appetite and body weight. The CART (cocaine- and amphetamine-regulated transcript) neuropeptide is an mRNA that changes in response to psychostimulant drug administration. Injection of CART peptides into the ventral tegmental area produces psychostimulant-like effects. CART localizes to areas of the central and peripheral nervous systems and is involved in feeding behavior when injected centrally. Expression of CART in the rat hypothalamus is modulated by nutritional status, and injection of synthetic CART peptide into the forebrain ventricular system suppresses food intake, indicating a possible role in hypothalamic control of energy homeostasis. Its identification in cell bodies and central terminals of vagal afferent neurons additionally suggests a role in brainstem mechanisms of meal termination and satiety.

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 C9orf50 gene product has been provisionally designated C9orf50 pending further characterisation.

Supplier: Bioss

C3orf37, also known as DC12 or MGC111075, is a 354 amino acid protein encoded by a gene that maps to human chromosome 3q21.3. Chromosome 3 is made up of approximately 214 million bases encoding over 1100 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 tumour 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.