28057 Results for: "2,4-Dichloro-3-formylpyridine&amp"

Supplier: Bioss

17Beta-HSD4 (17Beta-hydroxysteroid dehydrogenase type 4) is also known as peroxisomal multifunctional enzyme/protein 2 (MFE-2/MFP-2), D-bifunctional enzyme or 17-Beta Estradiol dehydrogenase type IV. It belongs to the 17Beta-HSD family of proteins that regulate the availability of steroids within various tissues throughout the body. 17Beta-HSD4 inactivates Estradiol through its oxidative activity but it is primarily involved in peroxisomal fatty acid and cholesterol Beta-oxidation. It has a multi-domain structure: the dehydrogenase domain is fused to a hydratase and a lipid transfer domain. 17Beta-HSD4 is a target protein of chromeceptin and it is essential for the downstream activation of Stat6. 17Beta-HSD4-deficient patients exhibit Zellweger-like syndrome and die within the first year of life. They display neuronal migration defects, facial dysmorphisms, severe hypotonia and convulsions in the neonatal period.

Supplier: Avantor Fluid Handling

Versatile washdown pumps for accurate fluid delivery – with an intuitive touch-screen interface.

Supplier: VWR International

The BA410 Elite Cytology Package is a complete cytology microscope bundle, which includes the Motic's flagship life-science microscope, the BA410 Elite. This package has been crafted to provide everything needed to perform professional level cytology microscopy with efficiency and effectiveness.

Supplier: VWR International

The microscope is for advanced work in life sciences. Sections, smears and dispersions can be checked by plan achromat objectives. Lab technicians profit from the Full-Kohler illumination, ready to work on unstained or weakly-stained structures from biology and medicine.

Supplier: Avantor Fluid Handling

Versatile pumps for accurate fluid delivery – with an intuitive touch-screen interface.

Supplier: VWR International

The VWR® Traceable® Logger-Trac™ Temperature datalogger is an ideal tool for monitoring material in transit, with a variety of intuitive user-programmable features and functions.

Supplier: Eppendorf

Eppendorf epT.I.P.S.® Racks feature high-precision pipette tips in 'Eppendorf Quality', 'PCR clean', 'Biopur®', and 'Sterile' purity grades. All tips are supplied in disposible racks designed for optimal organization and user convenience in demanding laboratory environments.

Supplier: Prosci

TRIM30 Antibody: TRIM30 belongs to a family of the tripartite motif (TRIM) proteins involved in the regulation of cell proliferation, differentiation, development, oncogenesis, apoptosis and antiviral responses. The TRIM protein family is an expanding family of RING ('really interesting new gene') proteins, also known as RBCC proteins as they contain an RBCC motif, which comprises a RING domain, one or two B-boxes and a predicted coiled-coil region. Studies have shown that some TRIM family members are critical to innate immunity; TRIM5, TRIM19 and TRIM25, for example, have been shown to restrict viral infection. A recent study shows that TRIM30 functions as a negative modulator of the TLR signaling pathway, by targeting TAB2 and TAB3, and contributes to the inhibition of TLR-mediated NF-kappa B activation. The importance of TRIM30 in the attenuation or termination of NF-kappa B activation suggests that targeting of TAB2 and TAB3 by TRIM30alpha may be a mechanism for modulating many types of immune responses.

Supplier: SenseAnywhere

Experience the SenseAnywhere StarterKit −30 to +70 °C, with the AiroSensor 20-20-25 for accurate temperature and RH tracking. Includes a secure Indoor AccessPoint, innovative AssetTagging, and 6 Credits for effortless sensor management, offering up to 10 years of maintenance-free, reliable monitoring across diverse environments.

Supplier: Electron Microscopy Sciences

Hard-Plus Resin-812 is supplied only as a premix kit

Supplier: Eppendorf

The Innova 44 and 44R (refrigerated) are Eppendorf’s most popular shakers - they accommodate flasks up to 5 L, have the space-saving glide-up door, and the reliable Innova triple-eccentric drive. They just run forever to give you peace of mind.

Supplier: DRG International

An enzyme immunoassay for the quantitative determination of caridac specific troponin I in serum.

Supplier: Eppendorf

The CryoCube® F101h ULT freezers offers a personal storage solution in a convenient package. The compact design means the unit will fit below a standard laboratory bench so samples are always securely close-at-hand. F101h has two inner compartments for storing for up to 6 racks/60 boxes giving space for up to 6000 vessels (1.5 ml). These freezers with efficient and reliable 2-stage compressor systems help reduce energy consumption, which helps to lower costs. Energy consumption: (–70/–80 ℃): 4.6/6.3 KWh/day.

Supplier: Bioss

Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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 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. The C19orf29 gene product has been provisionally designated C19orf29 pending further characterization.

Supplier: Rockland Immunochemical

Humanized Recombinant Anti-VEGFA ScFV fragment Antibody has been tested for use in Flow Cytometry, Western Blot, and ELISA. This antibody recognizes structured VEGF-A and will work in western blot when the protein has not been denatured with DTT or bMe. Although not tested, this antibody could be useful in in IHC and in in-vivo and other cellular assays. Specific conditions for reactivity should be optimized by the end user

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 C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.

Supplier: Thermo Fisher Scientific

Ideal for routine processing, these centrifuges combine exceptional capacity, ergonomics, and value with market-leading capabilities including unparalleled productivity and throughput, as well as exceptional ergonomics.

Supplier: Thermo Fisher Scientific

Heracell i CO₂ incubators with variable control of oxygen stimulate cell behaviors that are more predictive of the in vivo environment. Available in a choice of two ranges of O₂ control, 1 to 21% for physiological levels and 5 to 90% for hyperoxic studies.each is supplied with maintenance free zirconia oxide sensor is calibrated automatically and remains in place during the ContraCon high temperature decontamination, and a unique gas tight segmented inner door assembly enables access sections of the chamber without disturbing the entire environment to minimize recovery time, contamination risk, and gas consumption.

Supplier: Rockland Immunochemical

Apoptosis, also known as programmed cell death, plays major roles in development and normal tissue turnover in addition to tumor formation. Apoptosis is regulated by death domain (DD) and/or caspase recruitment domain (CARD) containing molecules and the caspase family of proteases. CARD domain containing cell death regulators include RAIDD, Apaf-1, caspase-9, and caspase-2. A novel CARD domain containing protein was recently identified and designated ARC for apoptosis repressor with CARD. An alternate splicing isoform of ARC was identified as Nop30. While ARC interacts with caspase-2 and -8 and suppresses apoptosis induced by cell death adapters FADD and TRADD and by cell death receptors Fas, TNFR-1 and DR3, Nop30 multimerizes and binds to the splicing factor SRp30c and may act to influence alternative splice site selection in vivo. The Nop30 antibody will not detect ARC protein.

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 C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.

Supplier: Labconco

Logic Class II, Type A2 Biosafety Cabinets (BSCs) offer comprehensive personnel, product and environmental protection from hazardous particulates, including risk group agents requiring BSL 1 to 4 containment. These cabinets are ideal for applications involving biological hazards, genetic material, antineoplastic drugs and other hazardous airborne particulates. All models ensure the highest standard of safety and performance.

Supplier: Eppendorf

Eppendorf's twin.tec® 96-well, 150 µl PCR Plates feature a polycarbonate frame and thin-walled polypropylene wells ensuring optimal heat transfer and high rigidity. The SafeCode variants enhance sample identification, while the BioBased options, manufactured using renewable resources, provide an eco-friendly alternative without compromising performance.

Supplier: Cytiva

Ettan™ IPGphor™ 3 is a fully integrated isoelectric focusing (IEF) system optimized to deliver high throughput, speed, reproducibility and high protein-loading capacity.

Supplier: Electron Microscopy Sciences

Home made devices are no longer necessary

Supplier: SenseAnywhere

The Hermetically Sealed Pt100 Probe, with a digital SenseAnywhere Bus and PFA seal, specializes in extreme temperature measurements in liquids, from –90 to +250 ˚C. Chemical-resistant and waterproof, it's perfect for harsh environments. It requires calibration only for the probe, with easy monitoring via the SenseAnywhere Portal.

Supplier: Analytik Jena US

The UVP iBox Studio is sophistication and ease of use in one system for high resolution small animal fluorescence imaging. From in depth in-vivo studies to quick screening, this powerful imaging system can perform any choice of in-vivo application.

Supplier: Bioss

Consisting of around 63 million bases with over 1,400 genes, chromosome 19 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 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. The C19orf29 gene product has been provisionally designated C19orf29 pending further characterization.

Supplier: MP Biomedicals

Bovine albumin is a single polypeptide chain consisting of approximately 583 to 595 amino acid residues and no carbohydrates. At pH 5-7 it contains 17 intrachain disulfide bridges and 1 sulfhydryl group.

Supplier: DRG International

A high sensitivity enzyme immunoassay for the quantitative determination of C-reactive protein (CRP) concentration in serum.

Supplier: Molecular Devices

Overcome the challenges associated with conventional cell confluence techniques with the CloneSelect Imager system - producing objective, quantitative, and consistent results in less time.