AGL Protein (Transcript Variant 4) (Myc-DYKDDDDK Tag)
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- Target See all AGL Proteins
- AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 4
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This AGL protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human AGL / GDE (transcript variant 4) 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 AGL 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
- AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
- Alternative Name
- Agl,gde (AGL Products)
- Synonyms
- DDBDRAFT_0219237 Protein, DDBDRAFT_0234114 Protein, DDB_0219237 Protein, DDB_0234114 Protein, GDE Protein, 1110061O17Rik Protein, 9430004C13Rik Protein, 9630046L06Rik Protein, AI850929 Protein, C77197 Protein, amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase Protein, glycogen debranching enzyme Protein, glycogen debranching protein Protein, amylo-1,6-glucosidase, 4-alpha-glucanotransferase Protein, AGL Protein, agl Protein, MMAH_RS03870 Protein, Agl Protein
- Background
- This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described.
- Molecular Weight
- 174.6 kDa
- NCBI Accession
- NP_000019
- Pathways
- Cellular Glucan Metabolic Process
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