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Image Unavailable-TCIAB1627-10G

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

Codice catalogo: (TCIAB1627-10G)
Fornitore: TCI EUROPE
Codice articolo fornitore: B1627-10G
Codice articolo locale: TCIAB1627-10G
Descrizione: N-ɑ-Boc-L-asparagine ≥98.0% (by HPLC, titration analysis)
UOM: 1 * 10 g
Image Unavailable-A16019.14

N-ɑ-Boc-L-asparagine ≥98%

Fornitore: Thermo Scientific
Descrizione: N-ɑ-Boc-L-asparagine ≥98%

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Image Unavailable-TCIAB3915-5G

N-ɑ-Boc-L-asparagine 4-nitrophenyl ester ≥98.0% (by HPLC)

Codice catalogo: (TCIAB3915-5G)
Fornitore: TCI EUROPE
Codice articolo fornitore: B3915-5G
Codice articolo locale: TCIAB3915-5G
Descrizione: N-ɑ-Boc-L-asparagine 4-nitrophenyl ester ≥98.0% (by HPLC)
UOM: 1 * 5 g
Image Unavailable-TCIAB2964-25G

Nɑ-(tert-Butoxycarbonyl)-D-asparagine ≥98.0% (by HPLC, titration analysis)

Fornitore: TCI EUROPE
Descrizione: Nɑ-(tert-Butoxycarbonyl)-D-asparagine ≥98.0% (by HPLC, titration analysis)

Image Unavailable-H61121.06

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

Fornitore: Thermo Scientific
Descrizione: Nɑ-(tert-Butoxycarbonyl)-D-asparagine 95%

Certificati

Image Unavailable-TCIAB3789-25G

Nɑ-tert-Butoxycarbonyl-N-γ-trityl-L-asparagine ≥98.0% (by HPLC, titration analysis)

Fornitore: TCI EUROPE
Descrizione: Nɑ-tert-Butoxycarbonyl-N-γ-trityl-L-asparagine ≥98.0% (by HPLC, titration analysis)

Image Unavailable-TCIAA1614-100MG

Nω-(2-Acetamido-2-deoxy-β-D-glucopyranosyl)-Nɑ-(tert-butoxycarbonyl)-L-asparagine ≥96.0% (by HPLC)

Codice catalogo: (TCIAA1614-100MG)
Fornitore: TCI EUROPE
Codice articolo fornitore: A1614-100MG
Codice articolo locale: TCIAA1614-100MG
Descrizione: Nω-(2-Acetamido-2-deoxy-β-D-glucopyranosyl)-Nɑ-(tert-butoxycarbonyl)-L-asparagine ≥96.0% (by HPLC)
UOM: 1 * 100 mg
Image Unavailable-TCIAA1685-100MG

Nω-(2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-Nɑ-(tert-butoxycarbonyl)-L-asparagine benzyl ester ≥97.0% (by HPLC)

Codice catalogo: (TCIAA1685-100MG)
Fornitore: TCI EUROPE
Codice articolo fornitore: A1685-100MG
Codice articolo locale: TCIAA1685-100MG
Descrizione: Nω-(2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-Nɑ-(tert-butoxycarbonyl)-L-asparagine benzyl ester ≥97.0% (by HPLC)
UOM: 1 * 100 mg
Image Unavailable-TCIAG0117-1G

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

Codice catalogo: (TCIAG0117-1G)
Fornitore: TCI EUROPE
Codice articolo fornitore: G0117-1G
Codice articolo locale: TCIAG0117-1G
Descrizione: Nɑ-Glycyl-DL-asparagine ≥98.0% (by titrimetric analysis)
UOM: 1 * 1 g
Image Unavailable-BOSSBS-13322R-FITC

Anti-MOGS Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-13322R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-FITC
Codice articolo locale: BOSSBS-13322R-FITC
Descrizione: 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
Image Unavailable-BOSSBS-13322R-A750

Anti-GCS1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-13322R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-A750
Codice articolo locale: BOSSBS-13322R-A750
Descrizione: 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
Image Unavailable-BOSSBS-13322R

Anti-GCS1 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-13322R)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R
Codice articolo locale: BOSSBS-13322R
Descrizione: 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
Image Unavailable-BOSSBS-13322R-A647

Anti-MOGS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-13322R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-A647
Codice articolo locale: BOSSBS-13322R-A647
Descrizione: 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
Image Unavailable-BOSSBS-13322R-CY7

Anti-MOGS Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-13322R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-CY7
Codice articolo locale: BOSSBS-13322R-CY7
Descrizione: 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
Image Unavailable-BOSSBS-13322R-A488

Anti-MOGS Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-13322R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-A488
Codice articolo locale: BOSSBS-13322R-A488
Descrizione: 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
Image Unavailable-BOSSBS-13322R-HRP

Anti-MOGS Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Codice catalogo: (BOSSBS-13322R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-13322R-HRP
Codice articolo locale: BOSSBS-13322R-HRP
Descrizione: 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
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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