Du søkte etter: N-alpha-Boc-L-asparagine

Produsent: Thermo Fisher Scientific

Beskrivelse: N-ɑ-Boc-L-asparagine ≥98%

HMS Sertifikater

Artikkenummer: (TCIAB1627-10G)

Produsent: TCI

Beskrivelse: N-ɑ-Boc-L-asparagine ≥98.0% (by HPLC, titration analysis)

UOM: 1 * 10 g

Tilbud

Artikkenummer: (TCIAB3915-5G)

Produsent: TCI

Beskrivelse: N-ɑ-Boc-L-asparagine 4-nitrophenyl ester 98,0 HPLC_ASSAY_METHOD

UOM: 1 * 5 g

Tilbud

Produsent: TCI

Beskrivelse: Nɑ-(tert-Butoxycarbonyl)-D-asparagine 98,0 HPLC, T

Produsent: Thermo Fisher Scientific

Beskrivelse: Nɑ-(tert-Butoxycarbonyl)-D-asparagine 95%

Sertifikater

Artikkenummer: (94341-100G)

Produsent: VWR Chemicals

Beskrivelse: Animal-free amino acid. Polar. Amide.

UOM: 1 * 100 g

HMS Sertifikater Tilbud

Produsent: TCI

Beskrivelse: Nɑ-tert-Butoxycarbonyl-N-γ-trityl-L-asparagine 98,0 HPLC, T

Artikkenummer: (TCIAA1614-100MG)

Produsent: TCI

Beskrivelse: Nomega-(2-Acetamido-2-deoxy-beta-D-glucopyranosyl)-Nalpha-(tert-butoxycarbonyl)-L-asparagine 96,0 HPLC_ASSAY_METHOD

UOM: 1 * 100 mg

Tilbud

Artikkenummer: (TCIAA1685-100MG)

Produsent: TCI

Beskrivelse: Nomega-(2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl)-Nalpha-(tert-butoxycarbonyl)-L-asparagine benzyl ester ≥97.0% (by HPLC)

UOM: 1 * 100 mg

Tilbud

Produsent: Thermo Fisher Scientific

Beskrivelse: L(+)-Asparagin, anhydrous 99%

HMS Sertifikater

Produsent: Thermo Fisher Scientific

Beskrivelse: L(+)-Asparagin 99%

HMS

Artikkenummer: (TCIAG0117-1G)

Produsent: TCI

Beskrivelse: Nɑ-Glycyl-DL-asparagine ≥98.0% (by titrimetric analysis)

UOM: 1 * 1 g

Tilbud

Artikkenummer: (BOSSBS-13322R-FITC)

Produsent: Bioss

Beskrivelse: Glycosylation of asparagine residues in Asn-X-Ser/Thr motifs in proteins commonly occur in the lumen of the endoplasmic reticulum (ER). Glucosidase I catalyzes the first step in the N-linked oligosaccharide processing pathway. It specifically removes the distal alpha 1,2-linked glucose residue from the Glc3-Man9-GlcNAc2 oligosaccharide precursor. Glucosidase I contains a short cytosolic tail, a single pass transmembrane domain and a large C-terminal catalytic domain located on the luminal side of the ER. Mutations in the gene encoding Glucosidase I result in the congenital disorder glycosylation (CDG-IIb), which is characterized by generalized hypotonia, dysmorphic features, hepatomegaly, hypoventilation, feeding problems, seizures and death. Two point mutations in the Glucosidase I gene have been identified and result in amino acid substitutions, namely Arg486Thr and Phe652Leu, that affect polypeptide folding and active site formation.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13322R)

Produsent: Bioss

Beskrivelse: Glycosylation of asparagine residues in Asn-X-Ser/Thr motifs in proteins commonly occur in the lumen of the endoplasmic reticulum (ER). Glucosidase I catalyzes the first step in the N-linked oligosaccharide processing pathway. It specifically removes the distal alpha 1,2-linked glucose residue from the Glc3-Man9-GlcNAc2 oligosaccharide precursor. Glucosidase I contains a short cytosolic tail, a single pass transmembrane domain and a large C-terminal catalytic domain located on the luminal side of the ER. Mutations in the gene encoding Glucosidase I result in the congenital disorder glycosylation (CDG-IIb), which is characterized by generalized hypotonia, dysmorphic features, hepatomegaly, hypoventilation, feeding problems, seizures and death. Two point mutations in the Glucosidase I gene have been identified and result in amino acid substitutions, namely Arg486Thr and Phe652Leu, that affect polypeptide folding and active site formation.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13322R-A647)

Produsent: Bioss

Beskrivelse: Glycosylation of asparagine residues in Asn-X-Ser/Thr motifs in proteins commonly occur in the lumen of the endoplasmic reticulum (ER). Glucosidase I catalyzes the first step in the N-linked oligosaccharide processing pathway. It specifically removes the distal alpha 1,2-linked glucose residue from the Glc3-Man9-GlcNAc2 oligosaccharide precursor. Glucosidase I contains a short cytosolic tail, a single pass transmembrane domain and a large C-terminal catalytic domain located on the luminal side of the ER. Mutations in the gene encoding Glucosidase I result in the congenital disorder glycosylation (CDG-IIb), which is characterized by generalized hypotonia, dysmorphic features, hepatomegaly, hypoventilation, feeding problems, seizures and death. Two point mutations in the Glucosidase I gene have been identified and result in amino acid substitutions, namely Arg486Thr and Phe652Leu, that affect polypeptide folding and active site formation.

UOM: 1 * 100 µl

Tilbud

Artikkenummer: (BOSSBS-13322R-A750)

Produsent: Bioss

Beskrivelse: Glycosylation of asparagine residues in Asn-X-Ser/Thr motifs in proteins commonly occur in the lumen of the endoplasmic reticulum (ER). Glucosidase I catalyzes the first step in the N-linked oligosaccharide processing pathway. It specifically removes the distal alpha 1,2-linked glucose residue from the Glc3-Man9-GlcNAc2 oligosaccharide precursor. Glucosidase I contains a short cytosolic tail, a single pass transmembrane domain and a large C-terminal catalytic domain located on the luminal side of the ER. Mutations in the gene encoding Glucosidase I result in the congenital disorder glycosylation (CDG-IIb), which is characterized by generalized hypotonia, dysmorphic features, hepatomegaly, hypoventilation, feeding problems, seizures and death. Two point mutations in the Glucosidase I gene have been identified and result in amino acid substitutions, namely Arg486Thr and Phe652Leu, that affect polypeptide folding and active site formation.

UOM: 1 * 100 µl

Tilbud