Du Søgte efter: EU00017VWRC


595  results were found

Sort Results

Listevisning Easy View (new)
SearchResultCount:"595"
Beskrivelse: E2-like enzyme which forms an intermediate with UFM1 via a thioester linkage.
Varenummer: BOSSBS-8372R-A350
UOM: 1 * 100 µl
Leverandør: Bioss


Beskrivelse: E2-like enzyme which forms an intermediate with UFM1 via a thioester linkage.
Varenummer: BOSSBS-8372R-A647
UOM: 1 * 100 µl
Leverandør: Bioss


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


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


Beskrivelse: E2-like enzyme which forms an intermediate with UFM1 via a thioester linkage.
Varenummer: BOSSBS-8372R-A680
UOM: 1 * 100 µl
Leverandør: Bioss


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


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


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


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


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


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


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


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


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


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


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


209 - 224 of 595