GALNS Protein (Myc-DYKDDDDK Tag)
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- Target See all GALNS Proteins
- GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This GALNS protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human GALNS protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product GALNS Protein
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- Application Notes
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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 - Comment
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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.
- Storage
- -80 °C
- Storage Comment
- 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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- Target
- GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
- Alternative Name
- Galns (GALNS Products)
- Synonyms
- GALNAC6S Protein, GAS Protein, GalN6S Protein, MPS4A Protein, mFLJ00319 Protein, galns Protein, zgc:158385 Protein, galactosamine (N-acetyl)-6-sulfatase Protein, galactosamine (N-acetyl)-6-sulfate sulfatase Protein, N-acetylgalactosamine-6-sulfatase Protein, galactosamine (N-acetyl)-6-sulfatase L homeolog Protein, GALNS Protein, Galns Protein, Celly_0425 Protein, galns.L Protein, galns Protein
- Background
- 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.
- Molecular Weight
- 55.4 kDa
- NCBI Accession
- NP_000503
- Pathways
- Glycosaminoglycan Metabolic Process
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