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Varenummer: (BOSSBS-8372R-CY5.5)

Leverandør: Bioss

Beskrivelse: E2-like enzyme which forms an intermediate with UFM1 via a thioester linkage.

UOM: 1 * 100 µl

Tilbud

Varenummer: (ROCKMB-101-0500)

Leverandør: Rockland Immunochemicals

Beskrivelse: Deoxyribonuclease I (usually called DNase I), is an endonuclease coded by the human gene DNASE1. DNase I is a nuclease that cleaves DNA preferentially at phosphodiester linkages adjacent to a pyrimidine nucleotide, yielding 5'-phosphate-terminated polynucleotides with a free hydroxyl group on position 3', on average producing tetranucleotides. It acts on single-stranded DNA, double-stranded DNA, and chromatin.

UOM: 1 * 1 Each

Tilbud

Varenummer: (BOSSBS-1702R-A680)

Leverandør: Bioss

Beskrivelse: May catalyse alpha-1,3 glycosidic linkages involved in the expression of Lewis X/SSEA-1 and VIM-2 antigens.

UOM: 1 * 100 µl

Tilbud

Varenummer: (90018.)

Leverandør: Biotium

Beskrivelse: 5-TRITC (Tetramethylrhodamine 5-isothiocyanate chloride) is spectrally similar to TAMRA (90022). The isothiocyanate reactive group reacts with primary or secondary amines to form a thiourea bond linkage.

UOM: 1 * 5 mg

Tilbud

Varenummer: (90024.)

Leverandør: Biotium

Beskrivelse: 5(6)-FAM SE (full name: 5-(and-6)-Carboxyfluorescein, succinimidyl ester mixed isomers) is an amine-reactive green fluorescent dye widely used for labeling proteins or other molecules that contain a primary or secondary aliphatic amine. The coupling reaction is usually carried out at pH 8-9.5. The amide linkage from the coupling reaction is much more stable than the thiourea linkage formed from the coupling of an amine and an isothiocyanate.

UOM: 1 * 100 mg

Tilbud

Varenummer: (BOSSBS-3975R-HRP)

Leverandør: Bioss

Beskrivelse: AMY2A belongs to the glycosyl hydrolase 13 family. Catalytic activity: endohydrolysis of alpha-D-glucosidic linkages in oligosaccharides and polysaccharides.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R-A680)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibres more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R-A647)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R-FITC)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-2305R)

Leverandør: Bioss

Beskrivelse: E2 EPF is a member of the ubiquitin conjugating enzyme family. It is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme dependent manner, a characteristic property of ubiquitin carrier proteins.

UOM: 1 * 100 µl

Tilbud

Leverandør: TriLink BioTechnologies

Beskrivelse: 2',3'-Dideoxycytidine-5'-O-(1-Thiotriphosphate) is a sugar modified nucleoside triphosphate where the 2' and 3' hydroxyl groups are absent, resulting in chain termination. This ddCTP analog also contains a 1-Thiotriphosphate which results in a nuclease resistant phosphorothioate linkage. The inability of polymerases to extend from a dideoxy nucleotide causes chain termination and is useful in antiviral research and in a variety of biotechnology applications.

New Product

Varenummer: (BOSSBS-4075R-A750)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibres more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R-CY3)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4075R-A350)

Leverandør: Bioss

Beskrivelse: Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-2305R-A647)

Leverandør: Bioss

Beskrivelse: E2 EPF is a member of the ubiquitin conjugating enzyme family. It is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme dependent manner, a characteristic property of ubiquitin carrier proteins.

UOM: 1 * 100 µl

Tilbud