Arylsulfatase B Protein (ARSB) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2714959

Produktdetails

Target: Arylsulfatase B (ARSB)

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses Arylsulfatase B Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Arylsulfatase B (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: Arylsulfatase B (ARSB)

Andere Bezeichnung: Arylsulfatase B (ARSB Produkte)

Synonyme: ASB Protein, G4S Protein, MPS6 Protein, 1110007C02Rik Protein, AI480648 Protein, As-1 Protein, As-1r Protein, As-1s Protein, As-1t Protein, As1 Protein, As1-r Protein, As1-s Protein, As1-t Protein, Asr-1 Protein, Ast-1 Protein, ARSB Protein, arylsulfatase B Protein, arylsulfatase Protein, arylsulfatase b Protein, ARSB Protein, Arsb Protein, RB348 Protein, LOC5566067 Protein, CpipJ_CPIJ011047 Protein, VDBG_03275 Protein, arsb Protein, LOC5579667 Protein

Hintergrund: Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Molekulargewicht: 56 kDa

NCBI Accession: NP_000037

Pathways: Glycosaminoglycan Metabolic Process