23808 Results for: "Bolton-Hunter+reagent+(sulpho-SHPP)&pageNo=11"

Supplier: Lovibond Tintometer

The Model F is a visual colorimeter designed to optimise the use of Lovibond® glass filters in order to express colourof the sample in terms of Lovibond® Red, Yellow, Blue and Neutral. It can be used for colour measurment of products which transmit light as well as for opaque solids powders and pastes. Typical applications include including fats and fatty oils, bleached lac, liquid chemicals and pharmaceuticals.

Supplier: Brand

PP.

Supplier: MICRONOVA

LDPE Micronova BinLiners™ are ideal for the collection and disposal of waste, collection and transportation of parts or raw materials, and storage in cleanrooms and controlled environments. Thickness of 1 to 6 mm available for a variety of applications; including covering equipment, holding production waste, document storage, lining large production totes and so on.

Supplier: VWR Collection

Ontworpen voor de bereiding van buffers, weefselkweekmedia, microbiologische media en andere biologische vloeistoffen. Deze vacuümfiltratiesystemen zijn voorzien van hoogwaardige PES-membranen met grote diameter voor gegarandeerde prestaties en maximale doorvoer. De volledige montage omvat een filtratie-eenheid en een opvangfles met een ergonomische vorm, gegoten vingergrepen en een gepatenteerde flesdop. Dankzij het centrifugebuis- en trechtersysteem kan de gebruiker vloeistoffen rechtstreeks in een buis van 15 of 50 ml filteren.

Supplier: VWR Collection

Eenvoudig te gebruiken, nauwkeurige tafelrefractometers voor gebruik in laboratorium- of productieomgevingen.

Supplier: 3M Food Safety

The 3M™ Petrifilm™ Lactic acid bacteria count plate is a time-saving, sample-ready plate designed to determine total lactic acid bacteria populations in food and environmental samples.

Supplier: Bioss

E3 ubiquitin-protein ligase that promotes the degradation of insoluble ubiquitinated proteins, including insoluble PAX6, poly-Gln repeat expanded HTT and poly-Ala repeat expanded ARX. Mediates PAX6 ubiquitination leading to proteasomal degradation, thereby modulating cortical neurogenesis. May also inhibit PAX6 transcriptional activity, possibly in part by preventing the binding of PAX6 to its consensus sequences. May contribute to the regulation of the intracellular level of HN (humanin) or HN-containing proteins through the proteasomal degradation pathway. Mediates MED15 ubiquitination leading to proteasomal degradation. May contribute to the innate restriction of retroviruses. Upon overexpression, reduces HIV-1 and murine leukemia virus infectivity, by suppressing viral gene expression. Antiviral activity depends on a functional E3 ubiquitin-protein ligase domain. May regulate TRIM5 turnover via the proteasome pathway, thus counteracting the TRIM5-mediated cross-species restriction of retroviral infection at early stages of the retroviral life cycle.

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 C1orf192 gene product has been provisionally designated C1orf192 pending further characterization.

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 C1orf189 gene product has been provisionally designated C1orf189 pending further characterization.

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 C1orf189 gene product has been provisionally designated C1orf189 pending further characterization.

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 C1orf192 gene product has been provisionally designated C1orf192 pending further characterization.

Supplier: EPPENDORF

For any application that requires sample/reaction mixing and heating the Eppendorf® ThermoMixer F family is what you need. Whether you work with 0,5/1,5/2,0 ml tubes or plates (MTP and DWP) the dedicated fixed blocks offer a perfect solution for your special application.

Supplier: Thermo Fisher Scientific

De Finnpipette™ F2 biedt superieure robuustheid en duurzaamheid zelfs in de meest veeleisende toepassingen.

Supplier: Portwest

Slim fitting work trousers that provides incredible comfort and flexibility. Reinforced knee panels with subtle articulation allow for increased freedom of movement whilst the ribbed waistband and elasticated hems ensure a universal fit. Additional features include pre-bent knees, a crotch gusset and multiple pockets ideal for the secure storage of phones, pens and tools.

Supplier: STEMCELL Technologies

Mouse monoclonal IgG1 antibody against mouse, rat, guinea pig CD90/CD90.1, Alexa Fluor® 488-conjugated.

Supplier: Air Liquide

These vessels are designed for long term storage of biological samples in straws, cryo-vials and bags. A variety of electronic options on all models rack or canister storage systems for the samples.
Made of aluminum and composite materials.

Supplier: TOSOH Bioscience

SkillPak 1 and 5 ml columns are designed for fast method development, resin screening or sample concentration. Pre-packed with TOYOPEARL®, TSKgel® or Ca++Pure-HA™ process chromatography media, these columns offer superior separation of biomelocules, such as monoclonal antibodies, proteins and oligonucleotides. SkillPak 50 and 200 ml pre-packed columns are the best solution for seamless scale up of methods developed on SkillPak 1 and 5.

Supplier: Portwest

Be seen and be comfortable in this excellent quality jacket. The unique lightweight material offers an unrivaled combination of breathability, waterproof, and windproof protection.

Supplier: Brand

PS, effen of met transparante voet. De platen zijn leverbaar met verschillende wellprofielen (ronde U-bodem, conische V-bodem, vlakke F-bodem of C-vormige vlakke bodem met gebogen randen), in verschillende kleuren en met verschillende oppervlaktebehandelingen.

Supplier: Portwest

This jacket is made from 300D Oxford Weave fabric (300 denier polyester yarn) which features a high abrasion and tear resistance. The PU coating on the inside makes the fabric durable and waterproof, while the outer has a water- and stain-repellant coating which helps keep the garment clean.

Supplier: Whatman products (Cytiva)

Het TurboBlotter™ systeem is een snelle blotter waarmee 'downward blots' kunnen worden uitgevoerd. Het systeem garandeert hoge-resolutieblotting van DNA en RNA. De conventionele opbouw van Northern/Southern blotting is hierbij omgedraaid om de zwaartekracht te kunnen benutten.

Supplier: EPPENDORF

Eppendorf Deepwell plates 96-well, 500 µl offer efficient sample handling with features like OptiTrack® matrix for rapid identification and g-Safe® technology for stability during centrifugation. SafeCode variants provide secure three-level coding, including error correction for reliable identification, ensuring flexibility and accuracy in experimental workflows.

Supplier: ProSci Inc.

SPG11 Antibody: Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders.  Spastic paraplegia with thinning of the corpus callosum (ARHSP-TCC) is a relatively frequent form of complicated hereditary spastic paraplegia (cHSP) in which mental retardation and muscle stiffness at onset are followed by slowly progressive paraparesis and cognitive deterioration. Mutations of the SPG11 gene encoding the spatacsin protein have been identified as a major cause of HSP-TCC. Spatacsin is a potential transmembrane protein that is phosphorylated upon DNA damage. It is expressed in all structures of the brain, with a high expression in the cerebellum. SPG11 mutations may occur more frequently in familial than sporadic forms of cHSP without TCC. Kjellin syndrome is found to be associated with mutations in not only the SPG15 gene but also SPG11 gene.  Recent studies show Parkinsonism may initiate SPG11-linked HSP TCC and that SPG11 may cause juvenile Parkinsonism.

Supplier: Portwest

The DX4 Baffle Gilet uses a body-mapped design to balance insulation and freedom of movement. Hard-wearing nylon front and back panels are padded with Insulatex to keep the core body area warm. Two zipped chest pockets, side entry pockets, and internal pockets offer plenty of secure storage space.

Supplier: Portwest

Portwest WX3 contemporary workwear is designed to the highest standards and offer a solution for everyday activity and working environments. Constructed with cutting edge fabrics giving superior abrasion resistance and exceptional all-day comfort. The WX3 work trousers are made from durable poly-cotton canvas fabric and includes triple stitched seams and stretch panelling providing excellent comfort and flexibility.

Supplier: GILSON

Deze ergonomische air-displacement pipet is ontworpen voor pipetteercomfort gedurende de hele dag. De herontworpen handgreep is licht en de vingersteun zorgt voor extra comfort.

Supplier: biotechrabbit

Het RTS (Rapid Translation System) is een schaalbaar in-vitro eiwitexpressieplatform dat een groot aantal eiwitten produceert voor karakteriseringsstudies, functionele analyses of structurele analyses. RTS maakt zowel de transcriptie als omzetting van High-Yield (HY) en celvrije, continu wisselende (CECF)-technologieën mogelijk met systemen gebaseerd op bacteriële (E. coli) of eukaryotische (tarwekiemen) cellysaten. RTS biedt het voordeel van een celvrij eiwitexpressiesysteem en elimineert hierbij de noodzaak voor laboratoria om vooraf en achteraf stappen te nemen die bij celgebaseerde expressiesystemen horen.

Supplier: STEMCELL Technologies

Mouse monoclonal IgG1 antibody against mouse, rat, guinea pig CD90/CD90.1, APC-conjugated.

Supplier: ProSci Inc.

SHP2 Antibody: Src homology-2 domain containing protein (SHP2) is a member of the protein tyrosine phosphatase (PTP) family, a protein family that contains signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. SHP2 contains two tandem Src homology-2 (SH2) domains, which function as phosphotyrosine binding domains either directly or through scaffolding intermediates such as the insulin-receptor substrate 1 (IRS-1). These SH2 domains mediate the interaction of SHP2 with its substrates, allowing SHP2 to dephosphorylate proteins that inhibit signaling kinases such as ERK1 and AKT. SHP2 is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Recent experiments have shown SHP2 plays a significant role in hepatoprotection and liver regeneration.

Supplier: Portwest

These fully waterproof anti-static bomber jackets provide multi-norm protection in hazardous conditions. These are designed with chemical resistance and a detachable hood.