3191 Results for: "Turkey+red+oil+sodium+salt&pageNo=59"
Ladies shorts, C.I., Design C, dark grey
Supplier: FRISTADS KANSAS
Short trousers made of 65% polyester and 35% cotton, with soft nap on reverse side.
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PermaSleeve® Heat-Shrink Labels for M610, M611, BMP61, M710 (with media adapter) and BMP71 (with media adapter)
Supplier: Brady
PermaSleeve® PS heat-shrink polyolefin (B-342) wire marking sleeves combine speed, ease of use, and permanence to create long-lasting, high-quality identification.
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Gilets, Fristads® PR54-521 Design A, royal blue
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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Gilets, Fristads® PR54-521 Design A, black
Supplier: FRISTADS KANSAS
Gilets made from 65% polyester and 35% cotton; napped inner.
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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.
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Bi-directional/Linear shakers, Varioshake series
Supplier: LAUDA
Shakers with bi-directional/linear motion, heavy duty, low noise, in a compact design.
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Trousers for men, C.I., Design C, black
Supplier: FRISTADS KANSAS
Robust trousers made from 65% polyester and 35% cotton, with soft nap on reverse side.
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Anti-FAM59A Rabbit Polyclonal Antibody
Supplier: ProSci Inc.
FAM59A Antibody: FAM59A, also known as GAREM, was initially identified through a mass spectroscoptic method that measures different phosphotyrosine states of proteins in response to different cell stimuli. FAM59A is a downstream molecule in the EGF signaling pathway that is tyrosine-phosphorylated, and this phosphorylation is needed for the binding of Grb2, an adaptor protein crucial to the transduction of growth signals from the plasma membrane to the nucleus. ERK activation in response to EGF stimulation is regulated by FAM59A in COS-7 and HeLa cells, and the overexpression of FAM59A stimulated cell proliferation and colony formation in soft agar, suggesting that FAM59A might be a critical protein with roles in ligand-mediated signaling pathway of the EGF receptor and the tumorigenesis of cells.
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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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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.
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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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Gilets, Fristads® PR54-521 Design A, royal blue
Supplier: FRISTADS KANSAS
Gilets made from 65% polyester and 35% cotton; napped inner.
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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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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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Overalls, Fristads® PR54-820, design A, royal blue
Supplier: FRISTADS KANSAS
Work overalls made from 65% polyester and 35% cotton. With napped inner.
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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.
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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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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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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.
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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 (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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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.
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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.
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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.
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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
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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Trousers, Originals 255K FAS
Supplier: FRISTADS KANSAS
Classic style trousers made of 100% long staple FAS® cotton twill. Suitable for all kind of craftsmen. Pockets exposed to wear and tear are reinforced with 100% polyamide.
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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.
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.