FA2H Protein (Myc-DYKDDDDK Tag)
-
- Target Alle FA2H Proteine anzeigen
- FA2H (Fatty Acid 2-Hydroxylase (FA2H))
- Protein-Typ
- Recombinant
-
Spezies
- Human
-
Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses FA2H Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
-
- Recombinant human Fatty acid alpha-hydroxylase protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product FA2H Protein
-
-
- Applikationshinweise
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Kommentare
-
The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Lagerung
- -80 °C
- Informationen zur Lagerung
- 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
- FA2H (Fatty Acid 2-Hydroxylase (FA2H))
- Andere Bezeichnung
- Fatty Acid alpha-Hydroxylase (FA2H Produkte)
- Synonyme
- FAAH Protein, FAH1 Protein, FAXDC1 Protein, SCS7 Protein, SPG35 Protein, RGD1310347 Protein, Wdr59 Protein, Faxdc1 Protein, G630055L08Rik Protein, MGC85470 Protein, MGC97767 Protein, cb1044 Protein, zgc:153777 Protein, fatty acid 2-hydroxylase Protein, fatty acid 2-hydroxylase L homeolog Protein, fatty acid hydroxylase Protein, FA2H Protein, Fa2h Protein, fa2h.L Protein, fa2h Protein, Tsp_11648 Protein, Ilyop_0703 Protein, Celly_1453 Protein, Weevi_1515 Protein, Fluta_1455 Protein, Mesop_3301 Protein
- Hintergrund
- This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.[provided by RefSeq, Mar 2010].
- Molekulargewicht
- 42.6 kDa
- NCBI Accession
- NP_077282
-