12096 Results for: "TLC+Plates&pageNo=17&view=easy"

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: Thermo Fisher Scientific

Use Thermo Scientific™ SureSTART™ 11 mm Snap caps with snap vials that have an 11 mm opening, including our SureSTART 2 ml glass snap Vials, 1.5 ml total recovery glass snap vials, high recovery glass snap vials, and glass snap micro vials for <2 ml samples (level 3).

Supplier: EPPENDORF

Versatile, ergonomic pipette with innovative design, meeting the highest needs in precision and accuracy.

Supplier: Thermo Fisher Scientific

Use Thermo Scientific™ SureSTART™ 9 mm screw caps with screw vials that have a 9 mm opening, including our SureSTART 2 ml Glass Screw Vials and 2 ml polypropylene screw Microvials for <2 ml samples (Level 1). Select level 1 caps for chromatography approved, cost optimised products that are suitable for everyday analyses and compatible with all instrument types.

Supplier: SIOEN

This multi-functional jacket with detachable sleeves and detachable fleece lining can be adapted to any kind of weather. It is made of Siopor® Ultra fabric (100% polyester fabric with 100% PU coating). With detachable fleece lining in body (can not be worn separately), fixed polyamide lining in body and quilted sleeves.

Supplier: Thermo Fisher Scientific

The Thermo Scientific™ F1-ClipTip™ pipette features interlocking technology to ensure secure tip attachment. The pipettes work exclusively with Thermo Scientific ClipTip pipette tips, providing a unique tip interface that locks the tip in place, and ensures a complete seal with minimal tip application and ejection forces. Tips are locked firmly in place and will not fall off.

Supplier: Portwest

This traditional t-shirt made of 50% polyester and 50% cotton offers optimum warmth at all times.

Supplier: RENTEX

Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, Comfort Stretch 285, 44 (men), Polyester/cotton, Beige, For men, 60% polyester, 35% cotton and 5% DOW XLA, Weight: 285 g/m², General Purpose, Industrial, Pockets: With pockets

Supplier: Antibodies.com

Monkey IL-17A Matched Antibody Pair Kit includes an unlabelled monoclonal capture antibody, biotin-labelled monoclonal detection antibody, Streptavidin-AP, recombinant human IL-17A ELISA standard, and standard reconstitution buffer. This matched antibody pair kit can be used to quantify native and recombinant non-human primates and human IL-17A. Matched antibody pair kits are ideal for economical ELISA and ELISA-based assay development.

Supplier: Antibodies.com

Mouse BCMA ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse BCMA in serum, plasma or other biological fluids.

Supplier: DuPont

These Tyvek® overalls are made from flash spun, high density polyethylene, providing an ideal balance of protection, durability and comfort. Tyvek® is permeable to both air and water vapour, yet repels water-based liquids and aerosols. It offers an excellent barrier against fine particles and fibres (down to 1 micron in size).

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Brady

Mark cables and wires with the B-427 self-laminating vinyl label material, designed with a clear self-laminating protective layer. Print almost anywhere with a durable Brady portable label printer.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Ansell

Unsupported neoprene gloves that provide broad chemical protection with enhanced comfort and tactility.

Supplier: LEICA MICROSYSTEMS

Emspira 3 digital microscope empowers users to streamline inspection processes, cover inspection needs flexibly, and work with confidence. An ideal partner for manipulation, quality control, inspection and research applications.

Supplier: Thermo Fisher Scientific

The Thermo Scientific™ IntelliStack™ CO₂ Incubator shaker is a versatile laboratory instrument used for incubating and agitating samples simultaneously. It combines the functions of an incubator and shaker, providing a controlled environment for cell culture, microbial growth, and various other applications. With adjustable temperature, speed, and CO₂ concentration settings, it offers precise control over experimental conditions. A large, easy-to-use 10" colour touchscreen display with alarms, alerts, real-time monitoring of key parameters, and data logging with export via USB or Ethernet allows for easy operation.

Supplier: Hospidex

Sharpsafe®, historic pioneer in protecting against the risk of sharps injuries and sustainability in medical waste packaging management, presents the recycled 5th generation needle containers.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: ELMA SCHMIDBAUER

The Elmasonic EASY ultrasonic bath series includes 9 units of different sizes and is characterised by simple, user-friendly operation. With 100% ultrasonic power at a frequency of 37 kHz, the EASY solves cleaning tasks quickly and efficiently. Ideal for removing tenacious, mineral soiling and polishing pastes.

Supplier: Copan

CLASSIQSwabs™ are traditional and sterile ready-for-use devices intended for the collection of clinical samples.  The association of Copan CLASSIQSwabs™ with the wide range of Copan Transport Media enables an efficient sample collection and preservation compatible with many downstream assays.
These soft fiber swabs are available in tubes or peel pouches, Regular or Minitip shapes, and various materials such as cotton, rayon, and polyester. All these materials are inert and non-toxic to microorganisms and patients. CLASSIQSwabs™ are traditional and sterile ready-for-use devices intended for the collection of clinical samples.

Supplier: ALSICO

Comfortable multirisk trousers in inherent flame retardant fabric.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Merck

MultiScreenHTS plates are specifically developed for high-throughput use with automated work stations. Rigid sidewalls improve handling and ample surfaces are provided for bar code labels. Wells are individually sealed to prevent incubation crosstalk and the underdrain is removable for access to the filters. Filter plates are available in 96- and 384-well platforms with a broad selection of membranes and plastics.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Bioss

CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four isoforms and encoded by a gene mapping to human chromosome 1. 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.

Supplier: Thermo Fisher Scientific

Armadillo™ 384-well PCR plates combine the rigidity of a polycarbonate frame with thin walled polypropylene wells to provide superior thermal cycling performance under all conditions, without warping. All formats are available with clear or white wells, ensuring the highest level of sensitivity for all PCR and qPCR reactions.

Supplier: LEICA MICROSYSTEMS

Leica (brightfield) colour cameras provide outstanding colour fidelity due to state-of-the-art colour interpolation algorithms performed in the camera head. Leica fluorescence cameras provide high sensor sensitivity allowing short exposure times and, therefore, preventing photo bleaching, so actively protecting cells from any photo damage.

Supplier: Avantor Fluid Handling

Versatile pumps for process applications – with an intuitive touch-screen interface and advanced connectivity.