PFAS Protein (Myc-DYKDDDDK Tag)
-
- Target See all PFAS Proteins
- PFAS (Phosphoribosylformylglycinamidine Synthase (PFAS))
- Protein Type
- Recombinant
-
Origin
- Human
-
Source
- HEK-293 Cells
- Purification tag / Conjugate
- This PFAS protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
-
- Recombinant human PFAS 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 PFAS Protein
-
Phosphoribosylformylglycinamidine Synthase (PFAS) (AA 1-1338) protein (Strep Tag)
Crystallography grade PFAS Origin: Human Host: Tobacco (Nicotiana tabacum) Recombinant >80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA
Phosphoribosylformylglycinamidine Synthase (PFAS) (AA 1-1337) protein (Strep Tag)Crystallography grade PFAS Origin: Mouse Host: Tobacco (Nicotiana tabacum) Recombinant ≥ 80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA
-
- Application Notes
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
-
The tag is located at the C-terminal.
- Restrictions
- For Research Use only
-
- 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.
-
- Target
- PFAS (Phosphoribosylformylglycinamidine Synthase (PFAS))
- Alternative Name
- Pfas (PFAS Products)
- Synonyms
- FGAMS Protein, FGARAT Protein, PURL Protein, 4432409B16Rik Protein, Gm18 Protein, Sofa Protein, phosphoribosylformylglycinamidine synthase Protein, phosphoribosylformylglycinamidine synthase (FGAR amidotransferase) Protein, Spirs_3128 Protein, PFAS Protein, Pfas Protein
- Background
- Purines are necessary for many cellular processes, including DNA replication, transcription, and energy metabolism. Ten enzymatic steps are required to synthesize inosine monophosphate (IMP) in the de novo pathway of purine biosynthesis. The enzyme encoded by this gene catalyzes the fourth step of IMP biosynthesis.
- Molecular Weight
- 144.6 kDa
- NCBI Accession
- NP_036525
-
