Supplier: Brady

High-performance polyester (B-488) withstands numerous solvents and variable temperatures when applied to various surfaces, including stainless steel and polypropylene.

Supplier: VWR Collection

Designed for freezing samples in all cryopreservation applications, these vials feature an internal thread with washer, or an external thread.

Supplier: Hettich

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

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: 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: 3M

The G3000 helmet is made from UV-stabilised ABS and was designed in close collaboration with forestry, industrial and construction workers. It is intended for use in harsh environments with tough demands for effective protection, excellent ventilation and a maximum field of vision.

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: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

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: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: Avantor

The Avantor® ACE® C18-AR phase utilises a specially developed ligand combining a C18 chain with integral phenyl functionality, thus combining the benefits of both C18 and phenyl characteristics into a single phase. This can be used for ‘standard’ C18 column separations, but is additionally recommended for separations that involve compounds containing aromatic functionality.

Supplier: Avantor Fluid Handling

High accuracy pressure transducers for plug and play connectivity with Masterflex® MasterSense® pump systems.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

Supplier: JSP

EVO® VISTAshield® is a next generation, feature-rich safety helmet based on the proven Evolution® head protection technology. Incorporating a fully retractable optical class 1 integrated face shield offering A-rated impact protection. The eyewear is easy to deploy, adjust and maintain, ensuring protection is on hand whenever it is required.

Supplier: Cole Parmer

Advanced split beam optics ensure excellent accuracy and reproducibility.

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: Avantor

These syringe filters are specifically designed for chromatography sample preparation applications and optimised to provide the most consistent results with less extractables.

Supplier: Bioss

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A 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

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.

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

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

Supplier: 3M

3M™ SecureFit™ Safety Helmet, X5000 series, provides secure, comfortable, and adjustable head protection for workers in a variety of situations. The helmets feature six different settings to adjust positions and 4-point chin strap selector systems to switch between EN 397 (industrial safety helmets) or EN 12492 (helmets for mountaineers) certification standards. X5000 series safety helmets are vented, brimless, and have 3M™ UVicator™ sensors that indicate levels of exposure to damaging ultraviolet (UV) light. The easily-adjustable, 6-point ratchet suspension system features the exclusive 3M™ pressure diffusion technology.

Supplier: 3M

3M™ Full Facepiece Reusable Respirator is multi-function full-face mask designed to provide durable and comfortable protection against a wide range of respiratory hazards. Use in conjunction with approved 3M powered air systems or as a negative pressure respirator with the 3M™ DT Series filter range, providing protection against a wide range of industrial hazards.

Supplier: Avantor

Avantor® ACE® C18-PFP phase utilises a specially developed ligand combining a C18 chain with integral PFP functionality. This results in a phase that maintains the hydrophobic, stability and low bleed characteristics of leading C18 phases, yet provides the multiple retention mechanisms of a PFP phase.