8804 Risultati per: "Alla France"

Supplier: Aviva Systems Biology

Anti-FANCL Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-FANCM Mouse Polyclonal Antibody

Supplier: US Biological

Anti-FANCF Goat Polyclonal Antibody

Supplier: Merck

Organic Standard, Methyl all-cis-5,8,11,14,17-eicosapentaenoate

Supplier: Merck

Organic Standard, all-cis-4,7,10,13,16-Docosapentaenoic acid

Supplier: VWR Chemicals

Marcatore MW (peso molecolare) per DNA, gamma alta: 10 frammenti da 1.503 a 48.502 bp. Materiale sufficiente per 75 – 150 saggi.

Supplier: Thermo Fisher Scientific

Polyethyleneimine, M.W. 1,800 ≥99%, branched

Supplier: Thermo Fisher Scientific

Nonenylsuccinic anhydride (mixture of branched chain isomers) 96%

Supplier: Avantor Fluid Handling

Displays instantaneous, total and accumulated flow rates.

Supplier: VWR Collection

These triple-display thermometers offer a choice of different probes. The bottle insulates the thermometer from rapid temperature changes when door is opened. The stainless steel handle probe (Ø×L: 3,2×300 mm) with 3 metre cable is waterproof and suitable for liquids, air/gas and semi-solids, with adjustable holder and VELCRO® tape.

Supplier: Merck

Acqua, Tracepur® for inorganic trace analysis, Supelco®

Supplier: Thermo Fisher Scientific

Germanio 99.999% (trace metals basis), in polvere

Supplier: Bioss

FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

Supplier: Thermo Fisher Scientific

Tallio (I) nitrato 99.99% (trace metals basis)

Supplier: Bioss

Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromsomal instability (1,2). The FA Group C complementation group gene encodes the protein FANCC, which is located in both cytoplasmic and nuclear compartments. FANCC is expressed in a cell cycle-dependent manner, with the lowest levels at the G1/S boundary and the highest levels in the M-phase. The FANCC protein interacts with other FA complementation group proteins as well as non-FA proteins (3). A human a spectrin II (designated aSpIIs) acts as a scaffold to enhance interactions between FANCC and FANCA to form a nuclear complex (4,5). Another binding partner of FANCC is the BTB/POZ domain containing protein FAZF, which is a transcriptional repressor (6). In hematopoietic cells expressing mutant FANCC, PKR is constitutively phosphorylated and has increased binding affinity for double-stranded RNA (7,8), which suggests that FANCC indirectly suppresses the activity of PKR. These cells are also apoptotic and are hypersensitive to IFNg and TNFa (8). In addition, FANCC protein is involved in the activation of STAT1 through receptors for at least three hematopoietic growth and survival factors (8).

Supplier: Bioss

Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromsomal instability (1,2). The FA Group C complementation group gene encodes the protein FANCC, which is located in both cytoplasmic and nuclear compartments. FANCC is expressed in a cell cycle-dependent manner, with the lowest levels at the G1/S boundary and the highest levels in the M-phase. The FANCC protein interacts with other FA complementation group proteins as well as non-FA proteins (3). A human a spectrin II (designated aSpIIs) acts as a scaffold to enhance interactions between FANCC and FANCA to form a nuclear complex (4,5). Another binding partner of FANCC is the BTB/POZ domain containing protein FAZF, which is a transcriptional repressor (6). In hematopoietic cells expressing mutant FANCC, PKR is constitutively phosphorylated and has increased binding affinity for double-stranded RNA (7,8), which suggests that FANCC indirectly suppresses the activity of PKR. These cells are also apoptotic and are hypersensitive to IFNg and TNFa (8). In addition, FANCC protein is involved in the activation of STAT1 through receptors for at least three hematopoietic growth and survival factors (8).

Supplier: US Biological

Anti-FANCC Rabbit Polyclonal Antibody (Biotin)

Supplier: US Biological

Anti-FANCB Rabbit Polyclonal Antibody (Biotin)

Supplier: Thermo Fisher Scientific

Litio nitrato 99.999% (trace metals basis)

Supplier: Thermo Fisher Scientific

Selenio biossido 99.8% (trace metals basis)

Supplier: Thermo Fisher Scientific

Selenio biossido 99.999% (trace metals basis)

Supplier: Bioss

Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. The thirteen FA proteins that have been characterized are important for regulating chromosomal stability and genome surveillance. Eight of these proteins, namely FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL and FANCM, comprise the FA core complex, which catalyzes a key reaction in DNA repair: the monoubiquitination of FANCD2. FANCM (Fanconi anemia, complementation group M) is a member of the DEAD-box helicase family of proteins and contains a DEAH helicase domain and a nuclease domain. Localizing to chromatin fractions, FANCM is phosphorylated in a cell cycle-dependent manner and is believed to function as an anchor, recruiting the FA core complex to chromatin. Mutations in the gene encoding FANCM can lead to Fanconi anemia.

Supplier: AAT Bioquest

Fluorometric methods based on the peptide substrates labeled with cleavable fluorophores have been widely used for assaying various proteases.

Supplier: ENTEGRIS

Multiple film frame shippers provide a safe and effective way to ship and store up to 25 wafers, or singulated die, mounted to film frames. Special applications include shipping 'diced' or thinned GaAs or GaP wafers as well as storage or shipment of wafers mounted to film frame. Replaceable top cover cushion allows for reuse of shipper. Shippers available for 300 mm, 200 mm and 150 mm film frame applications.

Supplier: Corning

Trace Elements B Solution has the same composition as Cleveland's Trace Element I.

Supplier: Merck

Trace Metals - Clay 1, Supelco®, Certified reference material, : N/A, Pkg of 50 g

Supplier: UVEX

These polycarbonate and cellulose acetate visors can be attached to helmets by using a length adapter and can be locked in three positions.

Supplier: VWR Collection

Tutte le sedie e gli sgabelli sono disponibili con base a raggi realizzata in acciaio tubolare a elevata resistenza, particolarmente robusto e duraturo. Il design piatto riduce il rischio di inciampare.

Supplier: Thermo Fisher Scientific

Cesio 99.95+% (trace metals basis)

Supplier: Abcam

Rabbit Polyclonal FANCA/FAA antibody. Suitable for IP, WB and reacts with Human samples. Immunogen corresponding to Synthetic Peptide within Human FANCA aa 1400 to C-terminus.