Order Entry
Poland
ContactUsLinkComponent
 

 

Gilets, Fristads® PR54-521 Design A, dark grey

Gilets, Fristads® PR54-521 Design A, dark grey

Supplier: FRISTADS KANSAS

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

Expand 1 Items
 
Work shorts, Icon 2020 Luxe

Work shorts, Icon 2020 Luxe

Supplier: FRISTADS KANSAS

Two-tone shorts with contrasting seams, made from 65% polyester and 35% cotton. Ideal for craftsmen and light industries.

Expand 1 Items
 
PCR plates, 96-well, Armadillo™

PCR plates, 96-well, Armadillo™

Supplier: Thermo Fisher Scientific

Rigid PC frame, thin-walled PP wells. Ultra-rigid 96-well PCR plates with rounded V-bottom wells designed for robotic applications.

Expand 1 Items
 
Overalls, Fristads® PR54-820, design A, navy blue

Overalls, Fristads® PR54-820, design A, navy blue

Supplier: FRISTADS KANSAS

Work overalls made from 65% polyester and 35% cotton. With napped inner.

Expand 1 Items
 
High purity hardened qualitative filter paper

High purity hardened qualitative filter paper

Supplier: Ahlstrom-Munksjö

Ahlstrom-Munksjö’s qualitative grades of filter paper are recommended for use in analytical methods which determine or identify particulate constituents of a mixture irrespective of the amount present. Qualitative filter papers are often used in routine separation work that still requires high purity and consistent performance. These filter papers covers a wide range of laboratory applications, as liquids clarification, qualitative analytical separations for precipitates and buffers filtration, and are also used for soil analysis and in food and beverage testing. Wet-strengthened grades contain a reinforcement agent that increases their resistance to rupture when wet, such as in vacuum filtration, and their resistance when filtering acidic solutions. High Purity hardened filter papers grades 1288 to 1291 are also produced from cellulose with an alpha content of nearly 100% resulting in an ash content of <0,1%.

Expand 1 Items
 

Workers jackets, C.I., Design C, royal blue

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.

Expand 1 Items
 
Combat trousers, C701

Combat trousers, C701

Supplier: Portwest

These basic work trousers for men can be used as a part of a uniform, in service and office environments. They are made of 65% polyester and 35% cotton.

Expand 1 Items
 
VWR®, Chemical Resistant Coats, Polyester/Hydro-Tec, Reusable

VWR®, Chemical Resistant Coats, Polyester/Hydro-Tec, Reusable

Supplier: VWR Collection

These anti-static coats are manufactured from 99% polyester fibres with 1% Hydro-Tec finish (carbon treated), which makes them both extremely durable and excellent for repelling dirt, oil, chemicals and water. All coats feature a stand-up collar, two side pockets and one breast pocket, all three protected by a flap.

Expand 1 Items
 
Poloshirt, Acode® BaseCamp 1721

Poloshirt, Acode® BaseCamp 1721

Supplier: FRISTADS KANSAS

Heavy piqué poloshirt made of 100% cotton (models in mottled grey are made of 90% cotton and 10% viscose). Pre-shrunk, ring-spun and combed.

Expand 1 Items
 
Poloshirt, Acode® Basecamp

Poloshirt, Acode® Basecamp

Supplier: FRISTADS KANSAS

Heavy men's piqué poloshirt made of 100% pre-shrunk, ring-spun and combed cotton. The model in grey melange is made of 90% cotton and 10% viscose.

Expand 1 Items
 
Gilets, Fristads® PR54-521 Design A, royal blue

Gilets, Fristads® PR54-521 Design A, royal blue

Supplier: FRISTADS KANSAS

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

Expand 1 Items
 
Gilets, Fristads® PR54-521 Design A, marine blue

Gilets, Fristads® PR54-521 Design A, marine blue

Supplier: FRISTADS KANSAS

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

Expand 1 Items
 

Workers jackets, C.I., Design C, black

Supplier: FRISTADS KANSAS

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

Expand 1 Items
 
Overalls, Fristads® PR54-820, design A, royal blue

Overalls, Fristads® PR54-820, design A, royal blue

Supplier: FRISTADS KANSAS

Work overalls made from 65% polyester and 35% cotton. With napped inner.

Expand 1 Items
 

Men shorts, C.I., Design C, dark grey

Supplier: FRISTADS KANSAS

These short trousers are made of 65% polyester and 35% cotton, with a soft nap on the reverse side. OEKO-TEX® certified.

Expand 1 Items
 
Gilets, Fristads® PR54-521 Design A, black

Gilets, Fristads® PR54-521 Design A, black

Supplier: FRISTADS KANSAS

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

Expand 1 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 
Bench top centrifuges and packages, Megafuge ST1 and ST1R Plus

Bench top centrifuges and packages, Megafuge ST1 and ST1R Plus

Supplier: Thermo Scientific

Thermo Scientific™ Megafuge ST1/ST1R Plus bench top centrifuges offer intuitive controls and versatility for power at every turn.

Expand 2 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 
Dissolved oxygen meter, handheld, FiveGo™ F4

Dissolved oxygen meter, handheld, FiveGo™ F4

Supplier: Mettler - Toledo

These portable meters provide high quality dissolved oxygen measurements with the simple click of a button. The robust and waterproof design makes the FiveGo instruments the perfect companion to get reliable measurement data even in harsh conditions. Ideal for mobile applications in the laboratory, at-line, or outdoors.

Expand 3 Items
 
Shakers, roller 6 and 10 (basic and digital)

Shakers, roller 6 and 10 (basic and digital)

Supplier: IKA

Roller shakers with 6 or 10 rolls, provide smooth rocking and rolling action, basic models have fixed speed, and the digital units feature infinitely adjustable speed. Used for mixing blood samples, solid and liquid suspensions and viscous samples. The unit can be used with all conventional tubes and cylindrical bottles. Easily removable attachments enable quick cleaning in case of sample spills.

Expand 4 Items
 
CAPRI Stretch Trousers

CAPRI Stretch Trousers

Supplier: ALSICO

Men's trousers with a modern, preshaped fitting that offers a professional look without compromising comfort. The fabric is powered by Alsiflex technology, which provides a unique combination of stretch, sustainability, and performance.

Expand 1 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (Cy7®)

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 
Self-Laminating Vinyl Wrap Around Labels for M610, M611, BMP61, M710 (with Media Adapter) and BMP71 (with Media Adapter)

Self-Laminating Vinyl Wrap Around Labels for M610, M611, BMP61, M710 (with Media Adapter) and BMP71 (with Media Adapter)

Supplier: Brady

Self-laminating vinyl (B-427) is an excellent material for wire and cable identification. This material has good clarity and conformability, and is self-extinguishing.

Expand 1 Items
 

Leica EZ4 W Stereo Microscopes

Supplier: LEICA MICROSYSTEMS

Educational stereo microscope for beginners in college and university Leica EZ4.

Expand 2 Items
 
Rotating shakers, Loopster basic and digital

Rotating shakers, Loopster basic and digital

Supplier: IKA

Rotators for smooth yet effective mixing, the basic model has fixed speed, and the digital unit features infinitely adjustable speed. Ideal for biological samples, particularly blood. Suitable for separating and mixing processes of powdered and liquid samples in tubes up to 50 ml. Easily removable attachments provide for quick cleaning in case of sample spills. Different optional attachments enable units to be used for a variety of applications.

Expand 2 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (Cy5®)

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 

Anti-TMEM59 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Supplier: Bioss

TMEM59 is a 144 amino acid protein 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.

Expand 1 Items
 
Recommended for You