Sie suchten nach: D-Galactosamine+pentaacetate

Artikel-Nr: (ABNOH00002588-D01P)

Lieferant: Abnova

Beschreibung: Anti-GALNS Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

Aktion

Artikel-Nr: (ABNOH00002588-D01)

Lieferant: Abnova

Beschreibung: Anti-GALNS Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

Aktion

Artikel-Nr: (ABNOH00002588-B01P)

Lieferant: Abnova

Beschreibung: Anti-GALNS Mouse Polyclonal Antibody

UOM: 1 * 50 µG

Aktion

Artikel-Nr: (PRSI19-318)

Lieferant: ProSci Inc.

Beschreibung: Anti-GALNT4 Rabbit Polyclonal Antibody

UOM: 1 * 100 µl

New Product Aktion

Artikel-Nr: (ABNOPAB7554)

Lieferant: Abnova

Beschreibung: Goat polyclonal antibody raised against synthetic peptide of GALNS.

UOM: 1 * 100 µG

Aktion

Artikel-Nr: (PRSI15-998)

Lieferant: ProSci Inc.

Beschreibung: Anti-B3GALT4 Rabbit Polyclonal Antibody

UOM: 1 * 50 µl

New Product Aktion

Artikel-Nr: (ANTIA84403-100)

Lieferant: ANTIBODIES.COM

Beschreibung: Goat polyclonal antibody to GALNS for ELISA and WB with samples derived from human.

UOM: 1 * 100 µG

New Product Aktion

Lieferant: Merck

Beschreibung: Lipopolysaccharides (LPSs) are characteristic components of the cell wall of Gram-negative bacteria.

Artikel-Nr: (ABNOH00002588-PW1)

Lieferant: Abnova

Beschreibung: This Immunopreciptitation/ Western Blot Antibody Pair set comes with one Antibody for Immunoprecipitation and another to detect the precipitated protein in Western Blot.

UOM: 1 * 1 SET

Aktion

Artikel-Nr: (PRSI46-663)

Lieferant: ProSci Inc.

Beschreibung: Anti-GALNS Goat Polyclonal Antibody

UOM: 1 * 100 µG

Aktion

Artikel-Nr: (BOSSBS-13269R-A647)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13269R-CY5)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13269R-HRP)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13269R-A350)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13269R-A555)

Lieferant: Bioss

Beschreibung: 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

Aktion

Artikel-Nr: (BOSSBS-13269R-FITC)

Lieferant: Bioss

Beschreibung: 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

Aktion