Arylsulfatase B Protein (ARSB) (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes Arylsulfatase B (ARSB) Protéines
- Arylsulfatase B (ARSB)
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant 2
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette Arylsulfatase B protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human Arylsulfatase B (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product ARSB Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- 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.
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- Antigène
- Arylsulfatase B (ARSB)
- Autre désignation
- Arylsulfatase B (ARSB Produits)
- Synonymes
- 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
- Sujet
- 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.
- Poids moléculaire
- 42.3 kDa
- NCBI Accession
- NP_942002
- Pathways
- Glycosaminoglycan Metabolic Process
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