11731 Results for: "Ace+Audio+Visual&pageNo=21&view=easy"

Supplier: Thermo Fisher Scientific

These columns offer lower hydrophobic retention than columns packed with longer alkyl length material, such as C18. Based on Core Enhanced Technology, they provide fast, high resolution separations without the elevated back pressures required by sub-2 µm particles. Improve separation speed and resolution while maintaining low backpressures using Thermo Scientific™ Accucore C8 columns.

Supplier: BASSAIRE

These laminar flow workstations have been designed to protect product and operating staff by maintaining a dust free ultra clean environment. The P-range is constructed in white powder coated high quality carbon steel with a 304 L stainless steel post formed worktop.

Supplier: HAMILTON BONADUZ

The 1800 series is the reinforced plunger version of the 1700 series syringe. Attached to the flange of the syringe is a removable blue syringe holder that prevents heat transfer, dispense inaccuracies and plunger blow outs. It also provides support to small volume plungers that are prone to bending during injection.

Supplier: OHAUS

The Ranger 7000 series are rugged, high performance industrial scales for the toughest jobs. Ten advanced application modes can provide results for complex applications while minimising manual calculations. Ranger 7000 will meet a variety of industrial applications from recipes formulation through automatic filling systems to density weighing of concrete. The scales have a bright backlit display and navigation panel that is comprised of a keypad with 5 quick, 8 function, and 12 alphanumeric keys and a 109 mm graphic display, which can be operated in multiple languages.

Supplier: SIOEN

Protective, bicoloured jacket made of 100% soft double-sided polyester fleece providing good cold protection. With anti-pilling treatment and stitched seams. Can be zipped into the rain jacket 608Z.

Supplier: Greiner Bio-One

Flexibility is critical in terms of modern liquid handling solutions. This is why the Sapphire tips are manufactured in eight different sizes in a volume range from 10 to 1250 µl, including an extended length 10 µl tip for the recovery of small sample volumes. All our tips are made of medical grade polypropylene and are available as standard, low-retention, filter, or low-retention filter tips.

Supplier: Boster Bio

APOBEC3G (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G) is a human enzyme encoded by the APOBEC3G gene. This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. The protein encoded by this gene has been found to be a specific inhibitor of human immunodeficiency virus-1 (HIV-1) infectivity.

Supplier: OHAUS

The Scout® SKX series has been designed for education applications. The overload protection and large backlit LCD, backed by education software makes the Scout® the ideal balance for the classroom. The integrated transportation lock protects the load cell from damage during stacking storage and transportation. Can be used either in battery-powered mode (4× AA batteries, not included) or via the AC adapter, with power saving auto shut-off function and low battery indicator. The SKX123 has an ingenious draught shield with an easy to remove top cover piece.

Supplier: Antibodies.com

Human POTED ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human POTED in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Whatman products (Cytiva)

Cellulose nitrate membranes, circles, plain. Recommended for the majority of routine applications, this membrane is manufactured under strictly controlled conditions.

Supplier: Antibodies.com

Human HDAC6 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human HDAC6 in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Antibodies.com

Human ABCB4 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human ABCB4 in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Antibodies.com

Human LY6G6F ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human LY6G6F in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: CleanAir by Baker

BioVanguard Green Line is a Class II cabinet range which offers simplicity, robustness and high reliability and ensures the highest level of protection for the operator, product and environment, minimising the hazards inherent with working with agents assigned to biosafety levels one, two and three. It is designed for microbiological research with biological agents (e.g. bacteria, viruses, etc) and allergens.

Supplier: Bioss

Transcription factors, OTX1 and OTX2, are two murine homologs of the Drosophila orthodenticle (OTD), show a limited amino acid sequence divergence. OTX1 and OTX2 play an important role during early and later events required for proper brain development in that they are involved in the processes of induction, specification and regionalization of the brain. OTX1 is involved in corticogenesis, sensory organ development and pituitary functions, while OTX2 is necessary earlier in development, for the correct anterior neural plate specification and organization of the primitive streak. OTX2 is also required in the early specification of the neuroectoderm, which is destined to become the fore-midbrain, and both OTX1 and OTX2 co-operate in patterning the developing brain through a dosage-dependent mechanism. A molecular mechanism depending on a precise threshold of OTX proteins is necessary for the correct positioning of the isthmic region and for anterior brain patterning. The genes which encode OTX1 and OTX2 map to human chromosomes 2p13 and 14q21-q22, respectively.

Supplier: Bioss

Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterisation.

Supplier: Bioss

Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf29 gene product has been provisionally designated C12orf29 pending further characterisation.

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 recognised 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 Fc 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

Capsid protein self-assembles to form an icosahedral capsid with a T=1 symmetry, about 22 nm in diameter, and consisting of 60 copies of three size variants of the capsid protein VP1, VP2 and VP3 which differ in their N-terminus. The capsid encapsulates the genomic ssDNA. Binds to host cell heparan sulfate and uses host ITGA5-ITGB1 as coreceptor on the cell surface to provide virion attachment to target cell. This attachment induces virion internalisation predominantly through clathrin-dependent endocytosis. Binding to the host receptor also induces capsid rearrangements leading to surface exposure of VP1 N-terminus, specifically its phospholipase A2-like region and putative nuclear localisation signal(s). VP1 N-terminus might serve as a lipolytic enzyme to breach the endosomal membrane during entry into host cell and might contribute to virus transport to the nucleus.

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 C1orf180 gene product has been provisionally designated C1orf180 pending further characterization.

Supplier: Bioss

Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (i.e. a photon, pheromone, odorant, hormone or neurotransmitter), while the effectors (e.g. adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein alhfa, beta and gamma polypeptides are encoded by at least 16, 4 and 7 genes, respectively. Most interest in G proteins has been focused on their a subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Evidence, however, has established an important regulatory role for the beta gamma subunits. It is becoming increasingly clear that different G protein complexes expressed in different tissues carry structurally distinct members of the gamma as well as the alhfa and beta subunits, and that preferential associations between members of subunit families increase G protein functional diversity.

Supplier: Bioss

Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (i.e. a photon, pheromone, odorant, hormone or neurotransmitter), while the effectors (e.g. adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein alhfa, beta and gamma polypeptides are encoded by at least 16, 4 and 7 genes, respectively. Most interest in G proteins has been focused on their a subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Evidence, however, has established an important regulatory role for the beta gamma subunits. It is becoming increasingly clear that different G protein complexes expressed in different tissues carry structurally distinct members of the gamma as well as the alhfa and beta subunits, and that preferential associations between members of subunit families increase G protein functional diversity.

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 C1orf95 gene product has been provisionally designated C1orf95 pending further characterization.

Supplier: Ahlstrom-Munksjö

Ahlstrom-Munksjö offers a full range of high quality cotton papers with high absorbency – ideal for chromatographic analysis and blotting methods with gel (Southern, Northern and Western Blots). Ahlstrom-Munksjö manufactures, both in Europe and in the US, absorbent papers made of the highest purity cotton linters. These media do not contain additive of any kind, thus preventing any contamination during the transfer steps.

Supplier: FRISTADS KANSAS

Durable trousers made of Denim fabric (100% cotton), coloured back unwashed. Reinforcements in black 100% polyamide. With reflective piping at back for visibility.

Supplier: FRISTADS KANSAS

Trousers made of 100% high quality cotton twill. The fluorescent material is made of 80% polyester and 20% cotton. The fabric is dirt-, oil and water-repellent. Reinforcement in 100% polyamide.

Supplier: SIOEN

Modern, lightweight jacket made of 2-layer bonded softshell fabric consisting of 100% polyester stretch and 100% polyester fleece inside. The jacket provides good protection from cold and wind and can be be zipped into different jackets.

Supplier: Antibodies.com

Human IL-22 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human IL-22 in serum, plasma, and other biological fluids.

Supplier: Antibodies.com

Human VILIP1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human VILIP1 in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: FRISTADS KANSAS

Industrial overall made of 65% polyester and 35% cotton, with soft nap on reverse side. The black overall is available with several different accent colours. The accent colour can be found on the top of the collar, on the inside front flap, on the pocket edges and and as a stripe on front and back.