MECR Polyclonal Antibody

Background:
The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy.

Research Area: Metabolism, Signal transduction

Synonyms:
AI195831, CGI 63, FASN2B, Homolog of yeast 2 enoyl thioester reductase, HsNrbf-1, HsNrbf1, mecr, MECR, Mitochondrial 2 enoyl thioester reductase, mitochondrial, NRBF 1, NRBF-1, NRBF1, Nuclear receptor binding factor 1, Nuclear receptor-binding factor 1, OTTMUSP00000009996, RP23-13A13.1, Trans 2 enoyl CoA reductase, mitochondrial, Trans-2-enoyl-CoA reductase

Immunogen: Fusion protein of human MECR

Swissprot: Q9BV79
Gene Accession: BC001419

Calculated MW: 40 kDa
Observed MW: Refer to figures

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 1.2 mg/mL
Dilution: WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.