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U heeft gezocht op: N-alpha-Boc-L-asparagine


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N-ɑ-Boc-L-asparagine ≥98%

Leverancier: Thermo Fisher Scientific
Omschrijving: N-ɑ-Boc-L-asparagine ≥98%

MSDS Certificaten

Image Unavailable-TCIAB1627-10G

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

Catalogus nummer: (TCIAB1627-10G)
Leverancier: TCI
Omschrijving: N-ɑ-Boc-L-asparagine ≥98.0% (by HPLC, titration analysis)
UOM: 1 * 10 g
Image Unavailable-TCIAB3915-5G

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

Catalogus nummer: (TCIAB3915-5G)
Leverancier: TCI
Omschrijving: N-ɑ-Boc-L-asparagine 4-nitrophenyl ester ≥98.0% (by HPLC)
UOM: 1 * 5 g
Image Unavailable-TCIAB2964-5G

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

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

Image Unavailable-H61121.06

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

Leverancier: Thermo Fisher Scientific
Omschrijving: Nɑ-(tert-Butoxycarbonyl)-D-asparagine 95%

Certificaten

Product Image-94341-100G

L(+)-Asparagine, anhydrous ≥99.0%, high purity

Catalogus nummer: (94341-100G)
Leverancier: VWR Chemicals
Omschrijving: Animal-free amino acid. Polar. Amide.
UOM: 1 * 100 g

MSDS Certificaten


Image Unavailable-TCIAB3789-25G

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

Leverancier: TCI
Omschrijving: 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)

Catalogus nummer: (TCIAA1614-100MG)
Leverancier: TCI
Omschrijving: Nω-(2-Acetamido-2-deoxy-β-D-glucopyranosyl)-Nɑ-(tert-butoxycarbonyl)-L-asparagine ≥96.0% (by HPLC)
UOM: 1 * 100 mg
Image Unavailable-B21473.36

L(+)-Asparagine, watervrij 99%

Leverancier: Thermo Fisher Scientific
Omschrijving: L(+)-Asparagine, watervrij 99%

MSDS Certificaten

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)

Catalogus nummer: (TCIAA1685-100MG)
Leverancier: TCI
Omschrijving: 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
Product Image-ACRO371601000

L(+)-Asparagine 99%

Leverancier: Thermo Fisher Scientific
Omschrijving: L(+)-Asparagine 99%

MSDS

Image Unavailable-TCIAG0117-1G

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

Catalogus nummer: (TCIAG0117-1G)
Leverancier: TCI
Omschrijving: 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))

Catalogus nummer: (BOSSBS-13322R-FITC)
Leverancier: Bioss
Omschrijving: 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)

Catalogus nummer: (BOSSBS-13322R-A647)
Leverancier: Bioss
Omschrijving: 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

Catalogus nummer: (BOSSBS-13322R)
Leverancier: Bioss
Omschrijving: 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)

Catalogus nummer: (BOSSBS-13322R-A750)
Leverancier: Bioss
Omschrijving: 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
Bel voor prijs
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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