3380 Wyniki dla: „Butle+plastikowe&pageNo=59&view=list”
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.
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Gilets, Fristads® PR54-521 Design A, marine blue
Supplier: FRISTADS KANSAS
Functional vests made from 65% polyester and 35% cotton; napped inner.
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Work trousers, Icon (Black, grey, white and green)
Supplier: FRISTADS KANSAS
Two-colour working trousers with contrast stitching, made of 65% polyester and 35% cotton.
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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.
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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.
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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%.
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Overalls, Fristads® PR54-820, design A, navy blue
Supplier: FRISTADS KANSAS
Work overalls made from 65% polyester and 35% cotton. With napped inner.
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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.
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Trousers, Crafts, Prostretch
Supplier: FRISTADS KANSAS
Working trousers made of 65% polyester and 35% cotton, with mechanical stretch. Brushed inside.
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Gilets, Fristads® PR54-521 Design A, black
Supplier: FRISTADS KANSAS
Gilets made from 65% polyester and 35% cotton; napped inner.
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Gilets, Fristads® PR54-521 Design A, dark grey
Supplier: FRISTADS KANSAS
Functional vests made from 65% polyester and 35% cotton; with napped inner.
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Conductivity meters, handheld, FiveGo™ F3
Supplier: Mettler - Toledo
These portable meters provide high quality conductivity 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.
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D3000 series particulate filters, Secure Click™
Supplier: 3M
3M™ Secure Click™ D3000 Series Particulate Filters feature a new dual flow design for easier breathing.
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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.
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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.
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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.
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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.
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Anti-TMEM59 Rabbit Polyclonal Antibody
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.
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Anti-TMEM59 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
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.
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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.
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Leica EZ4 W Stereo Microscopes
Supplier: LEICA MICROSYSTEMS
Educational stereo microscope for beginners in college and university Leica EZ4.
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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.
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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.
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Quintix® Pro Laboratory Balances
Supplier: Sartorius Balances
Quintix® Pro laboratory balances are not just about meeting your expectations but exceeding them. The balances have an array of premium features that enhance usability, flexibility, and incorporate an eco-friendly design.
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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.
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Anti-TMEM59 Rabbit Polyclonal Antibody (Cy3®)
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.
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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.
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Precision balances, Adventurer®
Supplier: OHAUS
A range of 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, dynamic weighing, parts counting, totalisation, density determination, check weighing and percentage weighing. Stabilisation times are typically less than two seconds.
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Dehydrated culture media
Supplier: Merck
Dehydrated media are used for a wide variety of applications. To minimise the risks associated with powdered culture media, the majority of Merck's dehydrated culture media is produced in granular form. Merck uses ingredients of non animal origin to minimise the potential risk of transmissible spongiform encephalitis (TSE). When there is no alternative, only ingredients which are recommended by EDQM, and belonging to TSE category B or C are used. This ensures that the product is of the highest quality and in compliance with the standards for food control, microbiological testing on finished products and starting materials, and quality control in the pharmaceuticals and cosmetics industries. Custom-made media can be prepared to meet individual customer specifications. The formulation is kept confidential via a Non Disclosure Agreement. Please enquire for further details. Advantages of granulated Merck media.
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Workers jackets, C.I., Design C, true navy
Supplier: FRISTADS KANSAS
Industrial jacket made of 65% polyester and 35% cotton, with soft nap on reverse side. The navy blue jacket is available with different accent and piping colours.