GALNS Antikörper

Produktnummer ABIN5708456

Produktdetails anti-GALNS Antikörper

Target: GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GALNS Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Aufreinigung: Antigen affinity purified

Immunogen: A recombinant human partial protein corresponding to amino acids Y181-N289 was used as the immunogen for the GALNS antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the GALNS antibody should be determined by the researcher.\. Western Blot: 0.5-1 μg/mL,IHC (FFPE): 1-2 μg/mL,Direct ELISA: 0.1-0.5 μg/mL

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Lagerung: -20 °C

Informationen zur Lagerung: After reconstitution, the GALNS antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Details zu GALNS

Target: GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))

Andere Bezeichnung: GALNS (GALNS Produkte)

Synonyme: GALNAC6S antikoerper, GAS antikoerper, GalN6S antikoerper, MPS4A antikoerper, mFLJ00319 antikoerper, galns antikoerper, zgc:158385 antikoerper, galactosamine (N-acetyl)-6-sulfatase antikoerper, galactosamine (N-acetyl)-6-sulfate sulfatase antikoerper, N-acetylgalactosamine-6-sulfatase antikoerper, galactosamine (N-acetyl)-6-sulfatase L homeolog antikoerper, GALNS antikoerper, Galns antikoerper, Celly_0425 antikoerper, galns.L antikoerper, galns antikoerper

Hintergrund: N-acetylgalactosamine-6-sulfatase is an enzyme that, in humans, is encoded by the GALNS gene. This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder.

UniProt: P34059

Pathways: Glycosaminoglycan Metabolic Process