AGPS Protein (Myc-DYKDDDDK Tag)
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- Target See all AGPS Proteins
- AGPS (Alkylglycerone Phosphate Synthase (AGPS))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This AGPS protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human AGPS / AAG5 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 AGPS 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
- AGPS (Alkylglycerone Phosphate Synthase (AGPS))
- Alternative Name
- Agps,aag5 (AGPS Products)
- Synonyms
- fd16e06 Protein, zgc:56718 Protein, wu:fd16e06 Protein, ADAP-S Protein, ADAS Protein, ADHAPS Protein, ADPS Protein, ALDHPSY Protein, 5832437L22 Protein, 9930035G10Rik Protein, AW123847 Protein, Adaps Protein, Adas Protein, Adhaps Protein, Adps Protein, Aldhpsy Protein, bs2 Protein, Adap-s Protein, Ads Protein, alkylglycerone phosphate synthase Protein, alkylglycerone phosphate synthase L homeolog Protein, agps Protein, AGPS Protein, agps.L Protein, Agps Protein
- Background
- This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.
- Molecular Weight
- 67 kDa
- NCBI Accession
- NP_003650
- Pathways
- SARS-CoV-2 Protein Interactome
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