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Image Unavailable-BOSSBS-13269R-A555

Anti-GALNS Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Référence Produit: (BOSSBS-13269R-A555)
Fournisseur: Bioss
Description: Chondroitinase is a 522 amino acid protein that localizes to the lysosome and functions as an exohydrolase that is essential for the degradation of glycosaminoglycans, keratan sulfate and chondroitin 6-sulfate. Using calcium as a cofactor, Chondroitinase, which exists as a disulfide linked oligomer, catalyzes the hydrolysis of the 6-sulfate group on target substrates. Defects in the gene encoding Chondroitinase are the cause of mucopolysaccharidosis type 4A (MPS4A), an autosomal recessive lysosomal storage disease that is characterized by the intracellular accumulation of keratan sulfate and chondroitin-6-sulfate and is associated with dental anomalies, short stature and, in some cases, death in the second or third decade of life.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-CY7

Anti-GNS Rabbit Polyclonal Antibody (Cy7®)

Référence Produit: (BOSSBS-13479R-CY7)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13269R-A750

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

Référence Produit: (BOSSBS-13269R-A750)
Fournisseur: Bioss
Description: Chondroitinase is a 522 amino acid protein that localizes to the lysosome and functions as an exohydrolase that is essential for the degradation of glycosaminoglycans, keratan sulfate and chondroitin 6-sulfate. Using calcium as a cofactor, Chondroitinase, which exists as a disulfide linked oligomer, catalyzes the hydrolysis of the 6-sulfate group on target substrates. Defects in the gene encoding Chondroitinase are the cause of mucopolysaccharidosis type 4A (MPS4A), an autosomal recessive lysosomal storage disease that is characterized by the intracellular accumulation of keratan sulfate and chondroitin-6-sulfate and is associated with dental anomalies, short stature and, in some cases, death in the second or third decade of life.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-CY3

Anti-GNS Rabbit Polyclonal Antibody (Cy3®)

Référence Produit: (BOSSBS-13479R-CY3)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A647

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

Référence Produit: (BOSSBS-13479R-A647)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-HRP

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

Référence Produit: (BOSSBS-13479R-HRP)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A680

Anti-Glucosamine 6 sulfatase Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Référence Produit: (BOSSBS-13479R-A680)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A555

Anti-GNS Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Référence Produit: (BOSSBS-13479R-A555)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A750

Anti-Glucosamine 6 sulfatase Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Référence Produit: (BOSSBS-13479R-A750)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A488

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

Référence Produit: (BOSSBS-13479R-A488)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-A350

Anti-GNS Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Référence Produit: (BOSSBS-13479R-A350)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13479R-FITC

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

Référence Produit: (BOSSBS-13479R-FITC)
Fournisseur: Bioss
Description: GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
UOM: 1 * 100 µl
Product Image-ACRO315250025

Calcium sulfate dihydraté 98+% ACS

Fournisseur: Thermo Fisher Scientific
Description: Calcium sulfate dihydraté 98+% ACS

FDS (Fiche de données de sécurité)

Product Image-ACRO448031000

Calcium sulfate dihydraté 98% pour biochimie

Fournisseur: Thermo Fisher Scientific
Description: Calcium sulfate dihydraté 98% pour biochimie

FDS (Fiche de données de sécurité)

Image Unavailable-SPCMCA170-2.5KG

Calcium sulfate dihydraté NF

Fournisseur: Spectrum Chemical
Description: Calcium sulfate dihydraté NF

Product Image-ACRO225270250

Calcium sulfate dihydraté 98+% pour analyses

Fournisseur: Thermo Fisher Scientific
Description: Calcium sulfate dihydraté 98+% pour analyses

FDS (Fiche de données de sécurité)

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