13518 Results for: "Prepared+Media+for+Microbiology&pageNo=18&view=easy"

Supplier: FRISTADS KANSAS

Overalls made from 65% polyester, 35% cotton, with soft nap on reverse side.

Supplier: Portwest

This classic style rain jacket is made of PVC coated polyester. It is designed to be worn in foul weather conditions.

Supplier: FRISTADS KANSAS

Trousers made from 100% cotton twill. Knee pockets made from 100% Cordura®.

Supplier: 3M

Designed with smart and intuitive features, the 3M™ Secure Click™ Half Mask Reusable Respirator is simple, comfortable and reliable. Available in three sizes: Small, medium and large. These respirators all come with an optional speaking diaphragm.

Supplier: Biotium

PMA (propidium monoazide) dye is a DNA modifier invented by scientists at Biotium. It is a photo-reactive dye that binds to dsDNA with high affinity. Upon photolysis with visible light, PMA dye covalently attaches itself to dsDNA.

Supplier: Roth Carl

SEKUROKA-UV-VOLLSICHTBRILLE ULTRAS. 1ST 1 * 1 ST

Supplier: Roth Carl

SEKUROKA-UV-VOLLSICHTBRILLE ULTRAS. 1ST 1 * 1 ST

Supplier: AGILENT

The AriaMx real-time PCR system is a fully integrated quantitative PCR amplification, detection and data analysis system.

Supplier: Bioss

C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Supplier: Bioss

Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.

Supplier: Brand

Fixed volume or variable volume, analogue-adjustable or digital easy calibration.

Supplier: MULTIROIR

Durable HDPE grating designed for laboratories. Its open-grid design ensures liquid drainage, minimizing slip risks. Resistant to chemicals and easy to disinfect, it supports strict hygiene standards. Quick to assemble with a clipping system, it’s ideal for safe, clean, and efficient lab environments.

Supplier: ROBU GLASFILTER

VitraPOR® quartz glass filters offer exceptional thermal and chemical resistance for demanding filtration tasks. Ideal for high-temperature and aggressive environments, they ensure precise particle retention with excellent purity and mechanical strength.

Supplier: Bioss

Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.

Supplier: Ansell

This knitted spandex/nylon liner features a foam nitrile coating on the palm. Under abrasive conditions the ultra-thin FORTIX™ nitrile foam coating lasts up to three times longer than comparable coatings, extending glove life and reducing total cost of ownership.

Supplier: Brady

For a tough and versatile general-purpose label material, look no further than the B-499 nylon cloth label material. Print almost anywhere with a Brady portable label printer.

Supplier: asecos

Fireproof safety cabinets, classified type 90 (fire resistant up to 90 minutes).

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.

Supplier: Bioss

C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Supplier: OHAUS

A range of four-place balances that incorporate a touch screen, advanced weighing and proximity sensor technologies. The easy to use control unit can be mounted on a base, above a base on an optional column, on a wall, or remotely (up to 3 metres distance with an optional cable). The touch screen display, with universal icons and informative prompts, simplifies set-up functions and basic operation. The operator has the added choice to use proximity sensors for hands-free operation when handling sensitive samples. These balances have multiple application modes from basic weighing to SQC applications, together with short stabilisation times and optimised performance specifications.

Supplier: Brand

Fixed volume or variable volume, analogue-adjustable or digital easy calibration.

Supplier: Bioss

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. The C1orf156 gene product has been provisionally designated C1orf156 pending further characterization.

Supplier: THERMO MATRIX TECHNOLOGIES

SepraSeal® and DuraSeal® capping systems offer a pierceable, individual tube sealing solution. They are made from thermoplastic elastomer (TPE) with colorants and are DMSO resistant.

Supplier: Ansell

AlphaTec® 04-005 Gloves are heavyweight PVC supported glove with better comfort, robust, long-cuffed PVC gloves, offering grip, comfort and chemical resistance.

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.

Supplier: Merck

The filters without binder resin retain their structural integrity without weight loss when heated up to 500 °C and can therefore be used in gravimetric analysis as well as for the filtration of hot gases.

Supplier: VWR Collection

Agilent OpenLab CDS is the next generation chromatography data system, designed for ease of use and productivity. OpenLab CDS offers the most comprehensive instrument control and data acquisition for Hitachi HPLC and amino acid analysers. In addition, it supports an expanded array of instrumentation from other vendors, for example Agilent LC, GC and LC/MS. Whether you like to control a single instrument or a huge network of different analytical instruments, OpenLab CDS grows with your needs.

Supplier: ROBU GLASFILTER

ROBU® Filter Crucibles with intergrated VitraPOR® filter provide efficient filtration for laboratory applications. Made from durable materials, these crucibles are designed for high-performance filtration, offering reliable separation of solids and liquids. Ideal for gravimetric analysis and other precise filtration processes.

Supplier: Bioss

C19orf18 is a 215 amino acid single-pass type I membrane protein that is encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.

Supplier: Bioss

Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.