Du Søgte efter: EU00017VWRC

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

Varenummer: BOSSBS-8372R-A350

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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

Varenummer: BOSSBS-8372R-A647

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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

Varenummer: BOSSBS-1702R-CY3

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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

Varenummer: BOSSBS-3975R

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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

Varenummer: BOSSBS-8372R-A680

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-CY5

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-CY5.5

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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.

Varenummer: BOSSBS-4075R-A680

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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]

Varenummer: BOSSBS-4075R

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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]

Varenummer: BOSSBS-4075R-A647

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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]

Varenummer: BOSSBS-4075R-FITC

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-A350

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-A680

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-FITC

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

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

Varenummer: BOSSBS-1702R-FITC

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud

Beskrivelse: Catalyzes the addition of fucose in alpha 1-6 linkage to the first GlcNAc residue, next to the peptide chains in N-glycans.

Varenummer: BOSSBS-6280R-HRP

UOM: 1 * 100 µl

Leverandør: Bioss

Tilbud