FA2H Protein (Myc-DYKDDDDK Tag)

Catalog No. ABIN2712286

Product Details

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Protein Type: Recombinant

Origin: Human

Source: HEK-293 Cells

Purification tag / Conjugate: This FA2H protein is labelled with Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Characteristics:

• Recombinant human Fatty acid alpha-hydroxylase protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Purity: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Application Details

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

Handling

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 Details

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Alternative Name: Fatty Acid alpha-Hydroxylase (FA2H Products)

Synonyms: 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

Background: 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].

Molecular Weight: 42.6 kDa

NCBI Accession: NP_077282