Supplier: Portwest

Breathable jacket made of 300 Denier polyester yarn which features superior abrasion and tear resistance. The PU coating on the inside makes the fabric durable and waterproof. The water- and stain-repellent coating on the outside helps to keep the garment clean. With nylon lining.

Supplier: RENTEX

Lab coats, Industrial coat, Lab coats, TrenkaTex®, 46 (men), Polyester/cotton, Blue, For men, 65% polyester and 35% cotton, with Sanfor®, Weight: 245 g/m², General Purpose, Pockets: With pockets, Closure type: Press studs / snaps

Supplier: FRISTADS KANSAS

Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.

Supplier: Portwest

These overalls made of Portwest Texo fabric (60% cotton, 40% polyester), provide complete lower body and leg protection. The cotton ensures the trousers wash well at 60 °C while the polyester gives a ruggedness essential for daily use.

Supplier: HAIX SCHUHE

The safety shoes are especially designed for road maintenance and construction site workers who place the highest demands on their work shoes. The shoe is made of extra thick waterproof bull leather of the highest quality, with a thickness of at least 2,0 mm. This leather strength makes HAIX safety shoes particularly robust. The work shoes ensure the all-round feet protection needed for working on road maintenance or construction sites. The composite protective cap made of ultralight, fibre-reinforced plastic protects the toes from injury by, for example, falling objects. The shape of the toe cap leaves enough space for your feet, ensuring not only safety but also comfort at work.

Supplier: TRENKA

Wind- and waterproof, breathable high-visibility winter parka made from light Airtech® material (100% polyester) with removable quilted polyester lining. Approved for industrial washing at 60 °C.

Supplier: Portwest

Stylish and practical work trousers made of cotton rich fabric (60% cotton, 40% polyester). The cotton ensures it washes well at 60 °C whilst the polyester gives a ruggedness essential for daily use. Can be twinned with TX10 contrast jacket.

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: 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, 46 (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: 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: 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: Avantor

Suitable for use on third party robotic instruments Hamilton Microlab Star and Nimbus. Available in conductive version, with or without filter, and in CE-IVD marked version for clinical diagnostic applications.

Supplier: Avantor

Avantor® ACE® UltraCore SuperPhenylHexyl solid-core (core-shell) particle columns are ideal for demanding MS work offering improved MS signal intensity and maximum MS response. These stainless steel columns combine high efficiency separations with low column back pressure. The Encapsulated Bonding Technology (EBT™) greatly increases the ligand coverage of the silica surface and effectively eliminates the effect of unbonded silanol groups on separations. This higher ligand coverage results in improved inertness, chromatographic performance and stability.

Supplier: LABCONCO

These glove boxes with stainless steel liner provide inlet and outlet ULPA filtration and a leak-tight physical barrier to protect the operator from exposure to potentially hazardous materials and perform work with contamination-sensitive materials under vacuum or in an inert environment. Available with two or four glove ports (double version).

Supplier: Bioss

CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two 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

CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two 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: LABCONCO

FreeZone® bench top freeze dryers are designed for lyophilising light to moderate sample loads. The compact design is ideal for laboratories with limited floor space.

Supplier: Bioss

Aldehyde dehydrogenases (ALDHs) mediate NADP+-dependent oxidation of aldehydes into acids during the detoxification of alcohol-derived acetaldehyde; metabolism of corticosteroids, biogenic amines and neurotransmitters; and lipid peroxidation. ALDH1A1, also designated retinal dehydrogenase 1 (RalDH1 or RALDH1), aldehyde dehydrogenase family 1 member A1, aldehyde dehydrogenase cytosolic, ALDHII, ALDH-E1 or ALDH E1, is a retinal dehydrogenase that participates in the biosynthesis of retinoic acid (RA). There are two major liver isoforms of ALDH1 that can localize to cytosolic or mitochondrial space. The ALDH1A2 (RALDH2, RALDH2-T) gene produces three different transcripts and also catalyzes the synthesis of RA from retinaldehyde. ALDH1A3 (ALDH6, RALDH3, ALDH1A6) is a 37 kb gene that consists of 13 exons and produces a major transcript of approximately 3.5 kb most abundant in salivary gland, stomach and kidney. ALDH3A1 (stomach type, ALDH3, ALDHIII) forms a cytoplasmic homodimer that preferentially oxidizes aromatic aldehyde substrates. ALDH genes upregulate as a part of the oxidative stress response, and appear to be abundant in certain tumors that have an accelerated metabolism toward chemotherapy agents.

Supplier: Greiner Bio-One

PS. With the exception of the Small Volume™, all 384-well PS microplates have rounded square wells, which combine the advantages of flexible working volume (10 to 130 µl) with reduced wicking and bubbling. Small Volume™ plates have round wells with a conical geometry, which allows a working volume of just 4 to 25 µl. All plates are supplied without lid, except for some sterile formats.

Supplier: Portwest

This fully certified waterproof jacket is a popular option across many industries. Made of PU coated polyester, 300D Oxford Weave, with a stain resistant finish. With nylon lining and polyester filling for additional warmth.

Supplier: IKA

Designed for cooling applications up to −20 °C with a powerful 400 W cooling capacity, these recirculating chillers are highly efficient and provide stable temperatures. With a wireless controller, it is possible to operate the RC 2 safely and comfortably irrespective of where the device is located.

Supplier: RENTEX

Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, 56 (men), Polyester/cotton, Hi-vis orange, For men, 60% cotton and 40% polyester, Weight: 270 g/m², HiVis, General Purpose, Industrial, Pockets: With pockets

Supplier: Thermo Fisher Scientific

Meet your certification and documentation needs with our level 2 Thermo Scientific™ SureSTART™ specification certified screw vial and cap kits. Select level 2 products for high throughput applications, when robustness and reproducibility are key.

Supplier: Bioss

Aldehyde dehydrogenases (ALDHs) mediate NADP+-dependent oxidation of aldehydes into acids during the detoxification of alcohol-derived acetaldehyde; metabolism of corticosteroids, biogenic amines and neurotransmitters; and lipid peroxidation. ALDH1A1, also designated retinal dehydrogenase 1 (RalDH1 or RALDH1), aldehyde dehydrogenase family 1 member A1, aldehyde dehydrogenase cytosolic, ALDHII, ALDH-E1 or ALDH E1, is a retinal dehydrogenase that participates in the biosynthesis of retinoic acid (RA). There are two major liver isoforms of ALDH1 that can localize to cytosolic or mitochondrial space. The ALDH1A2 (RALDH2, RALDH2-T) gene produces three different transcripts and also catalyzes the synthesis of RA from retinaldehyde. ALDH1A3 (ALDH6, RALDH3, ALDH1A6) is a 37 kb gene that consists of 13 exons and produces a major transcript of approximately 3.5 kb most abundant in salivary gland, stomach and kidney. ALDH3A1 (stomach type, ALDH3, ALDHIII) forms a cytoplasmic homodimer that preferentially oxidizes aromatic aldehyde substrates. ALDH genes upregulate as a part of the oxidative stress response, and appear to be abundant in certain tumors that have an accelerated metabolism toward chemotherapy agents.

Supplier: Bioss

CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two 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: BIOTIX

xTIP4™ is the only Rainin® LTS® compatible tip engineered with StarStop, a patented positive stop feature. This feature minimizes ejection force and reduces the risk of repetitive stress injuries (RSI).

Supplier: Bioss

CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two 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: Bohlender

b.safe caps together with fittings, tubing and an air valve form a perfect unit for solvent extraction from laboratory flasks.

Supplier: Bioss

CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two 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.